ZY

Zymeworks

- TSX:ZYME
Last Updated 2024-03-26

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Ticker Symbol Entity Name Domain As Of Date Title URL Brand Category Location Text City State Country Posted Date Number of Openings Description Salary Salary Currency Salary Description Coordinates Date Added Date Updated Company Name Sector Industry
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 23rd, 2019 12:00AM Manager, Regulatory Operations (Vancouver or Seattle) Open Regulatory Affairs Permanent - Full Time Seattle Washington USA Feb 27th, 2019 12:00AM <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"> </p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">About the Position</span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">The Manager, Regulatory Operations is responsible for supporting the preparation and submission of electronic regulatory documents (eCTD) in compliance with global health authority requirements. The position will ensure timely and compliant submissions of the highest quality, including clinical trial, i.e. CTAs, INDs, amendments, meeting briefing packages, periodic reports, safety reports and marketing applications (BLA/NDS/MAA). </span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">This position will report to the Vice President of Regulatory Affairs and will be based in either Seattle, WA or Vancouver, BC.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"> </p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Key Responsibilities</span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Responsible for the preparation, delivery and archiving of high quality global regulatory submissions in accordance with company standards and timelines.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Ensure submissions and related documentation are prepared in eCTD format and in compliance with applicable health agency regulations and guidelines.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Performance of high-level formatting in both word and PDF files, including the creation of bookmarks/hyperlinks, file optimization, optical character recognition, etc.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Review/validate submissions for compliance with technical requirements.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Maintain submission scheduling calendar to allow timely completion of projects.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Participate in submission team meetings.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Maintain the corporate submissions style guide and templates and ensure their use for regulatory submission documents.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Advise on regional and technical requirements for submission documents and provide answers to technical questions for submissions as needed.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Support the implementation of necessary regulatory publishing systems, including assistance with validations, qualifications and verifications of the systems.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Troubleshoot and resolve some technical issues with business-critical systems applications.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Maintain effective relationships with external publishing vendors/ contractors to help manage the regulatory submission workload.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Contribute to process improvement initiatives.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Maintain the files for electronic regulatory correspondence, ensuring that all communications are properly archived.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Contribute to the preparation and implementation of publishing processes and standards, and the updating/creation of the respective departmental SOPs and guidelines.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Stay current with relevant global regulatory submission requirements and publishing best practices.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"> </p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Qualifications and Experience</span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Bachelor’s degree.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• 7+ years of pharma/biotech industry experience with 5+ years of in-depth Regulatory Operations experience.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Highly knowledgeable in CTD/eCTD structure and requirements and a solid understanding of submission requirements for submission types (i.e. IND, CTA, BLA, NDS, MAA, PSUR, DSUR, etc.).</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Experience in compilation and publishing of US FDA eCTD submissions is required and experience with ex-US electronic submissions is highly desirable.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Detailed knowledge of and experience managing eCTD publishing systems, EDMS technology, publishing software and tracking databases.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Detailed knowledge of clinical/nonclinical data standards (ADaM, SDTM, SEND).</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Thorough understanding of the submission production process from beginning to end.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Strong knowledge of US and other major global (ICH, EU, Asian) regulatory requirements and standards and a thorough and current understanding of appropriate regulations.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Strong knowledge of Microsoft Office suite, Adobe Acrobat and Plug-Ins, EDMS, eCTD publishing tools, eCTD validation and viewing tools.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Ability to multi-task while paying close attention to detail and meeting deadlines.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Ability to work independently and as part of a team to accomodate changing timelines and priorities.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Excellent project management and organization skills.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Solutions oriented and pragmatic with analytical thinking and problem-solving skills.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Excellent communication and interpersonal skills.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"> </p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Why Work for Us?</span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at www.zymeworks.com. </span></span></p> <p style="font-size: 12px;font-family: -apple-system-font">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="color: #ffffff;font-family: verdana, geneva">#L1-JD1</span></p> Jun 23rd, 2019 07:52PM Jun 23rd, 2019 07:52PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 23rd, 2019 12:00AM Senior Project Manager (CMC) Open Project Management Permanent - Full Time Seattle Washington USA Mar 6th, 2019 12:00AM <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px"><b></b></span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px"><b>About the Position</b></span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks is looking for a highly motivated Senior Project Manager (CMC) who is a biopharma industry professional with experience in coordinating multiple complex CMC development plans.  Candidates will have the ability to partner with the Project Lead and multiple cross-functional team members to execute integrated project plans.  The Senior Project Manager will also be responsible for ensuring active communication of status, risk, risk management, and escalation of issue to stakeholders and management.  This position will report to the Director of Project Management (Development Programs). This position will be based in Seattle, WA.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px"></span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Key Responsibilities</span></span></strong></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Contributes to the strategic planning and direction of process development and manufacturing activities supporting development stage assets.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Facilitates the CMC project-planning process with input from technical lead team members; drives execution and monitors progress.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Leads the preparation of project budgets and facilitates appropriate review.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Maintains high level and detailed timelines of the CMC project plan and ensures that the functional resources and timelines are aligned with overall development program timelines.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Analyzes critical path, evaluates potential means to accelerate pace or mitigate identified risks and plans contingencies with input from various functions.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Prepares project progress reports, identifies and anticipates issues associated with project timeline and/or budget.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Creates communication plans, maintains open and proactive lines of communication with cross-functional and management stakeholders.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Regularly interacts with functional areas beyond CMC, such as Regulatory, Quality, Supply Chain, Technical Operations and Clinical</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Liaises with CMOs. Monitors and reports progress on SOWs; co-leads meetings; follows up on action items; organizes timely technical review of external meeting minutes.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Prepares and maintains project dashboards; assists with compilation of data packages to support business development, licensing, and intellectual property activities.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Prepares budgets and maintains forecasts.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Ensures team members understand project objectives, specifications, deliverables, timelines and tasks. </span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Contribute to the best practices of project management to support the continued success and evolution of the department</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Actively works to foster an environment of effective and collaborative working relationships amongst employees, management and external partners.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px"></span></span></p> <p><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Qualifications and Experience</span></span></strong></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>University degree and a minimum of 8 years related experience or an equivalent combination of education and experience. Broad pharmaceutical lifecycle management experience desirable.  PMP certification preferred.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Ability to lead through example and to establish an environment fostering effective and collaborative working relationships.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Excellent organizational skills and the ability to manage concurrent deliverables and work effectively in a challenging, milestone-driven environment.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Ability to refine project plan/timelines to meet critical milestones. </span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Ability to manage resources (budget, personnel, time).</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Proven personnel management and mentorship skills. </span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Strong oral, written and listening skills.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">•<span> </span>Proficiency with MS Office, utilization of PM software (MS Project or other gantting software).</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px"></span></span></p> <p><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Why Work for Us?</span></span></strong></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at www.zymeworks.com. </span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px"><span style="color: #ffffff">#L1-JD1</span></span></span></p> Jun 23rd, 2019 07:52PM Jun 23rd, 2019 07:52PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 23rd, 2019 12:00AM Executive Assistant Open Technical and Manufacturing Operations Permanent - Full Time Seattle Washington USA Mar 27th, 2019 12:00AM <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">Zymeworks is seeking a highly-motivated professional who is looking to grow their career with our company. </span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-size: 12px;font-family: 'times new roman', times"><strong><span style="font-family: -apple-system-font">About the Position</span></strong></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font"></span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">Zymeworks is looking for an Executive Assistant who will be responsible for managing and maintaining senior executive’s schedules, coordinating and preparing for meetings, preparing and editing various correspondence, coordinating travel arrangements, assisting with budgeting and organizing departmental events.  The successful candidate will be a seasoned professional who is confident, organized and a self-starter who excels in a high paced, rapidly changing environment while providing excellent customer service.  This position will report to the Executive Vice President, Early Development and Chief Scientific Officer, and the Senior Vice President, Technical and Manufacturing Operations. This position will be based in Seattle, Wa.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><strong><span style="font-family: -apple-system-font">Key Responsibilities</span></strong></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Manages and maintains executive’s schedule by planning and scheduling meetings, conferences, teleconferences and travel. </span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Optimizes schedule for maximum efficiency, prioritizes appointments and proactively resolves schedule conflicts. </span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Coordinates in-office meetings, prepares and circulates electronic and physical meeting materials and coordinates catering as required.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Collects and prepares presentation materials for Committee meetings.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Supports the scheduling and coordination of Board and Committee meetings, held on site and via teleconference.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Prepares and edits correspondence, communications, presentations and other documents.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Coordinates travel arrangements for Research and Technical &amp; Manufacturing Operations team members, as required. Manages domestic and international needs, including air and hotel reservations, ground transportation consistent with management preferences and corporate standards.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Assists with the onboarding of new employees, liaises with Office Manager to identify office/workspace allocation and set-up requirements and ensures workspace is equipped with appropriate reference materials and stationary supplies. </span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Assists in budget preparation, monitors expenses, generates purchase orders as required.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Completes executive expense claims and corporate credit card reconciliation as per the company guidelines and deadlines. </span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Complies with organizational policies and procedures necessary to ensure appropriate decision-making protocols are followed. </span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Proactively looks for new ways to improve current processes, maximize executive productivity and affect continuous improvement/efficiency within the reporting departments. </span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Organizes/coordinates events within the reporting departments, in accordance with agreed logistics, scope, timelines and budget allocations.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><strong>Education and Experience:</strong></span></p> <p></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">University degree in business, office administration, or a related program and a minimum of 5 to 10 years’ related experience or an equivalent combination of education and experience.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><strong><span style="font-family: -apple-system-font">Skills and Abilities:</span></strong></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team and to establish and maintain effective working relationships with employees, management and external associates.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Strong organizational skills and the ability to work effectively in a high paced, fast changing environment. Results-oriented.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Excellent customer service skills with a proactive, problem solving approach. Ability to function professionally and pleasantly during periods of high stress.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Demonstrates initiative and the ability to make thoughtful and timely decisions.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Ability to exercise professionalism, sound judgement and discretion when handling issues of a difficult sensitive or confidential nature.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Excellent oral and written communication skills. Strong attention to detail.</span></span></p> <p></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Experience coordinating domestic and international travel arrangements in multiple time-zones• Proficiency with MS Office and Sharepoint, including strong experience and familiarity with Outlook. Experience with Mac operating systems an asset.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">• Knowledge of NetSuite, Diligent, Bamboo, Veeva an asset.</span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><strong><span style="font-family: -apple-system-font">Why Work for Us?</span></strong></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><span style="font-family: -apple-system-font">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at www.zymeworks.com. </span></span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></p> <p><span style="font-size: 12px;font-family: 'times new roman', times"><strong><span style="font-family: -apple-system-font"></span></strong></span><span style="color: #ffffff;font-size: 12px;font-family: verdana, geneva">#L1-JD1</span></p> Jun 23rd, 2019 07:52PM Jun 23rd, 2019 07:52PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 23rd, 2019 12:00AM Director, Legal (Clinical) Open Legal Permanent - Full Time Seattle Washington USA Jun 20th, 2019 12:00AM <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-size: 14px;font-family: 'Source Sans Pro', arial, verdana, sans-serif"> Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></p> <p> Zymeworks is seeking a highly-motivated professional who is looking to grow their career with our company.  </p> <p>This position will report to the Senior Director, Legal (located in Vancouver, BC) and will be based in Seattle, WA.</p> <p><b>Key Responsibilities</b></p> <ul> <li>Participates in the development of strategic and long-term direction of the Legal department. Works with the Senior Director, Legal to develop and implement policies, programs, and processes. Ensures department and operational activities are aligned with company objectives. </li> <li>Drafts, reviews, and negotiates clinical trial agreements for global clinical trials, informed consent forms, HIPAA authorizations and other privacy consents, confidentiality agreements, CRO agreements, lab services agreements, drug supply agreements, manufacturing agreements, co-development and commercialization agreements, material transfer agreements, research evaluation agreements, investigator-sponsored trial agreements, and other agreements. Prepares negotiation strategy and back-up provisions for clinical trial contracts. </li> <li>Provides counsel concerning a broad range of legal, regulatory and compliance issues, including privacy law matters (HIPAA, GDPR, etc.), FDA regulations, False Claims Act, Anti-Kickback Statute, OIG guidance, the PhRMA Code and competition law, and anti-corruption law.  Advises on product labeling, launch activities, promotional and educational activities, marketing strategies, government reimbursement, and interactions with healthcare professionals.</li> <li>Assists the Senior Director, Legal to manage the activities of the company’s Contracts management team, and serves as a legal resource to Contracts management team.</li> <li>Maximizes company opportunities and minimizes risk and exposure by identifying legal trends and variances and communicating implications of the company’s activities. Analyzes, formulates and implements various strategies accordingly. </li> <li>As required, develops, manages, communicates and monitors the implementation of policies and procedures relating to clinical regulatory issues, and other legal and regulatory issues.</li> <li>Leads through example to establish an environment fostering effective and collaborative working relationships. </li> </ul> <p><b>Qualifications and Experience</b></p> <ul> <li>JD degree and a minimum of 10 years’ related experience, preferably including both prominent law firm and in-house experience supporting a clinical group at a biotechnology/pharmaceutical company, or an equivalent combination of education and experience. </li> <li>Member in good standing of a U.S. state bar, preferably the Washington State bar. </li> <li>Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team. Ability to establish and maintain effective working relationships</li> <li>Efficient, focused and pragmatic, offering quality practical legal advice and strategic solutions</li> <li>Strong leadership skills with the proven ability to manage, develop and empower employees</li> <li>Excellent organizational skills and the ability to manage competing priorities and concurrent deliverables and work effectively in a challenging, milestone-driven environment</li> <li>Ability to think and act strategically, anticipate roadblocks and map out next steps</li> <li>Sound business acumen with a practical, results-oriented management style that can translate innovative, creative strategies and conceptual thinking into action plans</li> <li>Demonstrated high level of integrity and ethics</li> <li>Extremely strong written and oral communication and presentation skills</li> <li>Positive, can-do attitude</li> </ul> <p><b>Why Work for Us?</b></p> <p>Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at <a href="http://www.zymeworks.com" rel="noopener noreferrer">www.zymeworks.com</a>. </p> <p>We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</p> Jun 23rd, 2019 07:52PM Jun 23rd, 2019 07:52PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 24th, 2019 12:00AM Senior Clinical Data Associate (Vancouver or Seattle) Open Biometrics Permanent - Full Time Seattle Washington USA Apr 13th, 2019 12:00AM <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">About the Position</span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"> </p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">Zymeworks is seeking a CDA to lead Data Management aspects of a clinical study with minimal support and oversight. The CDA will have thorough knowledge of FDA regulations and industry standards, strong technical skills, and is capable of leading infrastructure assessment and improvement. This position will report to the Senior Manager, Data Management and will be based in either Seattle, WA or Vancouver, BC.</span></span></p> <p><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">Key Responsibilities</span></span></strong></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Independently develops/reviews DM documents including but not limited to DMPs, CRFs, CRF Completion Guidelines, Edit Checks, UAT specifications, data flow and integrity plans, blinding plans, and data review plans.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Manages/coordinates work performed by vendors/CROs as appropriate to ensure quality of product. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• May assist in the selection of vendors (Lab, CRO).</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Programs non-system edit check (NSECs, data listings as appropriate), run SAS programs, review SAS logs, and generate output and/or SAS Data Listings as appropriate for SAS skill level.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Independently leads data cleaning activities such as but not limited to Study Team data reviews, Non-system Edit Check Output review, SAE reconciliation, and non-CRF data reconciliation.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Independently manages the database lock process in an efficient and timely manner;</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Understands critical tasks and milestones; ensures data management deliverables are met per study timelines. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Utilizes communication, available metrics reports, experience, knowledge, and other resources to efficiently lead and coordinate all data management activities.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Ensures study team members from different functional areas understand and deliver components affecting data to ensure successful execution of deliverables. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Provides solutions for data management issues that arise during study conduct. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Performs medical coding utilizing MedDRA and WHO-DRUG, as appropriate. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Evaluates CDM processes and applications for improvements.</span></span></p> <p> </p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Participate in working groups to develop and implement new processes and applications.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Coordinates and delegates work performed by junior CDAs, as needed; assists in mentoring junior CDAs and/or contractors. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Utilizes experience and leadership skills to provide guidance to other team members.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Fosters effective and collaborative working relationships with fellow employees, management and external partners.</span></span></p> <p><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">Qualifications and Experience:</span></span></strong></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• BA or BS in a relevant field and a minimum of 5 years’ related experience or an equivalent combination of education and experience</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Effective organizational skills and the ability to work effectively in a high paced, fast changing environment</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Ability to work collaboratively as a member of cross functional team.  Ability to establish and maintain effective and working relationships </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Technologically savvy; ability to quickly learn and implement new information, standards, regulations, tools, methods or software as it relates to position and profession </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Detail oriented; performs quality and accurate work </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Thorough knowledge of FDA regulations, ICH GCP guidelines, SDTM, CDISC, database development, UAT, medical coding, the drug development process </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Previous relevant electronic systems as such EDC, IXRS, RTSM</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Previous vendor/CRO management </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• SAS programming experience </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">Preferred: </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Previous experience with EPRO, SharePoint, JReview, Business Intelligence tool</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Database development experience </span></span></p> <p><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">Why Work for Us?</span></span></strong></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at www.zymeworks.com. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></span></p> <p><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">How to Apply</span></span></strong></p> <p> </p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">If you are interested in this challenging opportunity, please apply online at xxx. Due to the high volume of applicants, only those selected for interviews will be contacted.</span></span></p> Jun 24th, 2019 03:48PM Jun 24th, 2019 03:48PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 24th, 2019 12:00AM Senior Patent Agent/Lawyer Open Intellectual Property Permanent - Full Time Seattle Washington USA May 30th, 2019 12:00AM <p><span style="font-size: 12px;font-family: helvetica">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics. Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></p> <p><span style="font-size: 12px;font-family: helvetica">We are currently seeking a highly-motivated professional to join our Intellectual Property (IP) team as a Senior Patent Agent/Lawyer. This position will be based in Seattle, WA and will report into our Lead Patent Agent who is located in our headquarters in Vancouver, BC. </span></p> <p><span style="font-size: 12px;font-family: helvetica"> <b style="color: #000000;font-family: helvetica">Key Responsibilities</b></span></p> <ul> <li><span style="font-size: 12px;font-family: helvetica">Collaborates with the IP team to develop and manage the company’s global patent portfolio, including evaluating invention disclosures, drafting and prosecuting patent applications and conducting Freedom to Operate and patentability searches. </span></li> <li><span style="font-size: 12px;font-family: helvetica">Develops patent strategies for assigned products and platform technologies. </span></li> <li><span style="font-size: 12px;font-family: helvetica">Prepares and prosecutes PCT, US and foreign patent applications, working with lead patent agents and outside counsel as appropriate.  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Meets with scientists and engineers on a frequent basis to identify and protect novel inventions.  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Provides guidance and oversight to inventors for drafting invention disclosures and developing experimental protocols to support patents.  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Advises assigned R&amp;D project teams and business development teams on a wide range of IP matters, including analysis of patent landscape and third-party patent portfolios.</span></li> <li><span style="font-size: 12px;font-family: helvetica">Manages existing patent portfolio requirements and monitors deadlines for assigned cases.</span></li> <li><span style="font-size: 12px;font-family: helvetica">Performs patentability and Freedom to Operate searches.</span></li> <li><span style="font-size: 12px;font-family: helvetica">In conjunction with lead patent agents, assists in IP due-diligence examinations with collaborators, partners and investors. </span></li> <li><span style="font-size: 12px;font-family: helvetica">Participates on teams evaluating potential candidates for in-licensing.</span></li> <li><span style="font-size: 12px;font-family: helvetica">Monitors and analyzes competitive intellectual property and communicates findings to Lead Patent Agents.</span></li> <li><span style="font-size: 12px;font-family: helvetica">Develops, implements and ensures compliance of policies and procedures relating to IP protection requirements and ensures IP processes are consistent with best practices.</span></li> <li> <span style="font-size: 12px;font-family: helvetica">Actively works to foster an environment of effective and collaborative working relationships amongst employees, management and external partners. </span> </li> </ul> <p><span style="font-size: 12px;font-family: helvetica"><b>Qualifications and Experience</b> </span></p> <ul> <li><span style="font-size: 12px;font-family: helvetica">Requires an advanced degree in Molecular Biology, Structural Biology, Immunology, Biochemistry, Organic Chemistry, Medicinal Chemistry or related discipline, working knowledge of antibody-based therapeutics and/or small molecule therapeutics and a minimum of 5 years’ in a law firm and/or in-house IP department with a focus on drafting and prosecuting PCT, US and foreign patent applications, providing patentability and freedom-to-operate opinions or an equivalent combination of education and experience. PhD and post-doctoral experience preferred.  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Patent Agent licensed/admitted to practice before the USPTO and/or CIPO. </span></li> <li><span style="font-size: 12px;font-family: helvetica">Proven interpersonal skills with the ability to work collaboratively as a member of cross-functional team. Ability to establish and maintain effective working relationships  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Strong organizational skills and the ability to work effectively in a high paced, fast changing environment.</span></li> <li><span style="font-size: 12px;font-family: helvetica">Results-oriented  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Solid understanding of the rules, regulations and procedures of the U.S. Patent and Trademark Office  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Experience drafting and prosecuting patent applications  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Experience running complex prior-art/Freedom to Operate searches   </span></li> <li><span style="font-size: 12px;font-family: helvetica">Exceptional oral and written communication skills and the ability to present findings with confidence to senior management   </span></li> <li><span style="font-size: 12px;font-family: helvetica">Excellent attention to detail   </span></li> <li><span style="font-size: 12px;font-family: helvetica">Strong analytical and problem-solving abilities  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Demonstrated high level of integrity and ethics  </span></li> <li><span style="font-size: 12px;font-family: helvetica">Proficiency with MS Office  </span></li> </ul> <p><span style="font-size: 12px;font-family: helvetica"><b>Why Work for Us?</b></span></p> <p><span style="font-size: 12px"><span style="color: #000000;font-family: helvetica">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at </span><a style="font-family: helvetica" href="http://www.zymeworks.com/" rel="noopener noreferrer">www.zymeworks.com</a><span style="color: #000000;font-family: helvetica">. </span> </span></p> <p><span style="font-size: 12px;font-family: helvetica">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></p> Jun 24th, 2019 03:48PM Jun 24th, 2019 03:48PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 25th, 2019 12:00AM Associate Director, Clinical Quality Assurance (Vancouver or Seattle) Open Quality Assurance Permanent - Full Time Seattle Washington USA Apr 16th, 2019 12:00AM <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">Zymeworks is seeking an Associate Director, Clinical Quality Assurance to provide Quality oversight in support of Zymeworks’ clinical development programs and contribute to the development and ongoing management of the Zymeworks Quality Management System (QMS). This position will report to the Director, Quality Assurance and will be based in either Seattle, WA or Vancouver, BC</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">Key Responsibilities</span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"><em><span style="font-family: -apple-system-font"><span style="font-size: 12px">Leadership &amp; Partnership</span></span></em></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Leads the Zymeworks Clinical Quality Assurance team to ensure development and implementation of clinical Quality processes, procedures and standards as required by applicable regulations.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Provides ongoing development of the Clinical Quality Assurance (CQA) team, including staff selection, work assignments, goal completion, and performance management.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Establishes strong partnership/relationship with internal Zymeworks stakeholders and interacts frequently with senior management.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Recognized as a senior strategic GCP Quality resource.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Establishes and ensures adherence to budget, schedules and work plans.</span></span></p> <p><em><span style="font-family: -apple-system-font"><span style="font-size: 12px">Oversee Clinical Vendor Audit &amp; Compliance Monitoring Programs</span></span></em></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Develops and implements the clinical vendor audit plan in collaboration with Clinical Development.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Determines acceptability of potential clinical vendors.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Evaluates existing clinical vendors for compliance with GCP regulations, guidelines, and standards.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Ensures consistency of audit reports (i.e. observations and ratings).</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Provides Quality Assurance leadership and influence to product development teams.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Acts as the company-wide resource for Clinical Quality GCP, ICH guidelines, and Clinical Operations SOPs</span></span></p> <p><em><span style="font-family: -apple-system-font"><span style="font-size: 12px">Assess State of GCP Compliance</span></span></em></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Supervises and oversee the analysis of audit program results, quality issues and investigations in order to optimize regional operations and global state of compliance. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Collaborates with Quality Management and Quality Systems Quality Assurance to identify and mitigate GCP quality and compliance issues with potential systemic impact.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Monitors and interprets compliance issues identified across clinical programs and elevates systemic problems with appropriate recommendations/solutions to senior management for immediate and long-term resolution.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Provides appropriate risk analysis for key stakeholders to make critical decisions.</span></span></p> <p><em><span style="font-family: -apple-system-font"><span style="font-size: 12px">Regulatory Inspection / External Audit Support</span></span></em></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Represents Clinical Quality Assurance during GCP regulatory inspections and audits. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Assures observation responses are timely and appropriate to maintain good standing with regulatory agencies and partners.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Coaches and educates external sites and cross functional Zymeworks staff in clinical regulatory inspection readiness activities. </span></span></p> <p><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">Qualifications and Experience</span></span></strong></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Bachelor’s degree in Biology, Chemistry or other relevant discipline;</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• A minimum of eight (8) years’ related experience in the pharmaceutical/biotech industry with demonstrated increasing responsibility and relevant Quality Assurance experience or an equivalent combination of education and experience.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Four (4) years of Good Clinical Practices (GCP) auditing experience.</span></span></p> <p><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">Skills and Abilities:</span></span></strong></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Proven interpersonal skills with the ability to work collaboratively as a member of cross-functional team. Ability to establish and maintain effective working relationships.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Working knowledge of regulatory guidelines and expertise in Quality for the advancement of therapeutics through different phases of development.  </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Excellent organizational skills and the ability to manage concurrent deliverables and work effectively in a challenging, milestone-driven environment. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Proficiency with creating Standard Operating Procedures and working with Contract Research Organizations.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Advanced understanding of Quality principles, GCP regulatory requirements, industry standards and guidelines.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Strong understanding of Good Documentation Practices and GCP quality review methods.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Demonstrated ability to interact with cross-functional teams in order to ensure the compliance of the GCP operations.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Understanding of basic scientific/technical concepts.</span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Strong oral, written and listening skills. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">• Proficiency with MS Office.</span></span></p> <p><strong><span style="font-family: -apple-system-font"><span style="font-size: 12px">Why Work for Us?</span></span></strong></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at www.zymeworks.com. </span></span></p> <p><span style="font-family: -apple-system-font"><span style="font-size: 12px">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></span></p> <p> </p> Jun 25th, 2019 04:45PM Jun 25th, 2019 04:45PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 25th, 2019 12:00AM Vice President, Translational Sciences (Vancouver or Seattle) Open Translational Sciences Permanent - Full Time Seattle Washington USA May 11th, 2019 12:00AM <p style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span style="font-family: Titillium">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></p> <p style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><b><span style="font-family: Titillium">About the Position</span></b></p> <p style="font-size: medium;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #222222;font-size: 11.5pt;font-family: Titillium">Zymeworks</span><span lang="EN-US" style="color: #222222;font-size: 11.5pt;font-family: Cambria, serif"> </span><span lang="EN-US" style="color: #222222;font-size: 11.5pt;font-family: Titillium">is looking for a Vice President of Translational Sciences to join our Senior Management team. </span><span lang="EN-US" style="color: #222222;font-size: 11.5pt;font-family: Titillium">This executive position will lead the Pharmacokinetics, Biomarkers, Pharmacology, Toxicology, and Translational Informatics groups and is responsible for leading the transition of the organization’s drug discoveries into early stage and late stage development programs.</span></p> <p style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-family: Titillium">This position will report to the Chief Scientific Officer and Executive Vice President, Research &amp; Development and will be based in either Seattle, WA or Vancouver, BC</span></p> <p style="font-size: medium;font-family: 'Times New Roman', serif"><b><span style="font-family: Titillium">Key Responsibilities</span></b></p> <ul> <li style="font-size: medium;font-family: 'Times New Roman', serif"> <span style="font-size: 11pt;font-family: Titillium">In collaboration with the senior management team, develops the strategy and leads</span><span style="font-size: 11pt;font-family: Cambria, serif"> </span><span style="font-size: 11pt;font-family: Titillium">company efforts in translational sciences (transition of the organization’s drug discoveries into early stage and late stage development programs) including in vivo Pharmacology, biomarker discovery and IND enabling studies.</span> </li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Provides leadership to the PK, Biomarker, Pharmacology, Toxicology and Translational informatics groups, nurturing a culture of engagement, respect and high performance within a team environment. Provides leadership, coaching and feedback; mentors and empowers personnel.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Develops models, both preclinical and clinical, to ensure robust decision making on developability of drug molecules in various therapeutic areas of interest.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Conceives and executes translational strategies to support advancing discovery projects into clinical development programs; providing the link between early research and the clinical.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Oversees design of proof of concept studies and full development for various therapeutic area programs.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Serves as point-person accountable for translational strategy and biomarkers discovery on projects and multi-functional clinical program teams.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Works in conjunction with the biomarker lead to plan and execute a CDx plan as appropriate.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Develops, manages and implements operating budget for Translational Medicine, ensuring the financial resources are effectively allocated and managed to support achievement of the strategic objectives.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Participates as a key member of Zymeworks Research Leadership team.</span></li> <li style="font-size: medium;font-family: 'Times New Roman', serif"><span style="font-size: 11pt;font-family: Titillium">Oversees the development of detailed work plans to incorporate quantitative, objective end points into clinical studies to demonstrate target engagement, pharmacodynamic regulation of pathways of interest, modulation of pharmacologic mechanism and information to aid patient selection.</span></li> </ul> <p style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><b><span style="font-family: Titillium">Qualifications and Experience</span></b></p> <p style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="font-size: 11pt;font-family: Titillium">University degree in Translational Medicine, Immunology or related field and 15+ years’ industrial experience or an equivalent combination of education and experience.</span></p> <p style="font-size: medium;font-family: 'Times New Roman', serif"><b><span style="font-family: Titillium">Skills and Abilities</span></b></p> <ul> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Demonstrated ability to think holistically and long-term across a broad spectrum of industry trends and issues. Ability to envision, shape and communicate long term business objectives and priorities and be able to create competitive and break-through strategies and plans</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Excellent analytical and conceptual thinking abilities, forward-looking. Out-of-the-box problem solving skills</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Proven history of building relationships and fostering engagement across multiple stakeholders, including the board, senior management, operational levels, suppliers and business partners</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Exceptional leadership skills and the ability to mentor and develop strong contributors. A track record of inspiring and aligning organizations around goals and contributing as an active role model in company values</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Experience collaborating with biologists and chemists to generate <i>in vivo</i>target validation data and establishing PK/PD and biomarker correlations</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Experience with identifying relevant translational disease models and applying them to meet program goals</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Multiple examples of partnering with drug discovery to identify and develop candidates</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Strong track record of meeting and exceeding goals. Demonstrated ability to drive steep change as well as incremental, continuous improvements in quality, efficiency and growth through change initiatives and vigorous leadership</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Sound business acumen with a practical, results-oriented leadership style that can translate innovate, creative strategies and conceptual thinking into action plans</span></li> <li style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span lang="EN-US" style="color: #1d1d1d;font-size: 11pt;font-family: Titillium">Demonstrated high level of integrity and ethics</span></li> </ul> <p style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><b><span style="font-family: Titillium">Why Work for Us?</span></b></p> <p style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span style="font-family: Titillium">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at </span><span lang="EN-US"><a style="color: #954f72" href="http://www.zymeworks.com/" rel="noopener noreferrer"><span lang="EN-US" style="font-family: Titillium"><span lang="EN-US">www.zymeworks.com</span></span></a></span><span style="font-family: Titillium">. </span></p> <p style="font-size: medium;text-align: justify;font-family: 'Times New Roman', serif"><span style="font-family: Titillium">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></p> Jun 25th, 2019 04:45PM Jun 25th, 2019 04:45PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 27th, 2019 12:00AM Senior Manager, Clinical Supply Chain (Vancouver or Seattle) Open Technical and Manufacturing Operations Permanent - Full Time Seattle Washington USA Jan 19th, 2019 12:00AM <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">About the Position</span></span></strong></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks is currently seeking a Senior Manager, Clinical Supply Chain to join our Commercial Operations group. The successful candidate will be part of a highly motivated multidisciplinary group responsible for ensuring that clinical drug supply is available for global clinical trials, including compliance with international regulatory standards applicable to the storage, transport and labeling of antibody-based therapeutics and antibody-drug conjugates.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">This role includes demand forecasting, inventory management at depots and sites, order management and proof of delivery, return or destruction and global distribution logistics including import and export management. This position will also be responsible for leading the clinical labeling and packaging strategy for all materials needed for global clinical studies by working closely with Clinical Operations, CMC and contracted CROs and CMOs to determine manufacturing and supply needs and timelines.</span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">The successful candidate will have a background in clinical and commercial supply chain practices as well as a familiarity with the applicable GMP and ICH Quality guidelines governing biotherapeutics, and the abilty to incorporate multiple variables into forecasts and presentations. Effective communication and discussion with team members and other groups will be a critical component of daily activities. </span></span></p> <p style="font-size: 12px;font-family: -apple-system-font"> </p> <p style="font-size: 12px;font-family: -apple-system-font"><span style="font-family: verdana, geneva"><span style="font-size: 12px">The Senior Manager, Clinical Supply Chain will be based in either Seattle, WA or Vancouver, BC.</span></span></p> <p><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Key Responsibilities: </span></span></strong></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Leads the supply management of all Zymeworks clinical products including demand planning and supply for clinical global studies, management of the labeling and packaging supply chain, and distribution of product to clinical sites.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Develops strong internal collaboration with stakeholders, including CMC, Clinical Operations, Regulatory Affairs, Quality, and Process Development functions, to ensure effective cross-functional communication.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Manages clinical packaging and labeling including label design, translation and production.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Creates and manages a supply plan to support the pharmaceutical product demand forecast, including determination of supply overage amounts and regular inventory updates to project teams.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Develops supply strategy to maximize supply efficiency, minimize waste while identifying risk and develop risk mitigation plans.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Manages domestic and international distribution/logistics for clinical programs, including import and export of clinical supplies.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Establishes and maintains Supply Chain department SOPs, including packaging, labeling, logistics and others, in compliance with internal and regulatory standards and requirements.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Manages external clinical packaging/distribution vendors, including negotiating third-party contracts, and developing the distribution instructions with clinical supply chain vendors.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Monitors drug expiration and initiates supply/re-supply to clinical sites, serving as the inventory manager.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Achieves operational objectives by providing information and recommendations to strategic plans and budget reviews, and supporting department budget activities.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Participates as required in the vetting, evaluation and selection process for clinical inventory systems in conjunction with clinical operations and other cross-functional stakeholders.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Works with Quality Assurance to ensure Supplier Quality requirements are achieved and maintained.</span></span></p> <p><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Skills and Abilities:</span></span></strong></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• University degree and a minimum of 8 years’ related experience in clinical or commercial biologics global supply chain management or equivalent combination of education and experience.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team. Ability to establish and maintain effective working relationships</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Excellent organizational skills and the ability to work effectively in a high paced, fast changing environment</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Proven experience with forecasting, demand/supply planning, inventory management, clinical, packaging, labeling and distribution including cold chain, import/export and reverse logistics</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Experience in CMO and CRO vendor management</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Working knowledge of the clinical drug development process (Phase I-III)</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Working knowledge of cGMPs and familiar with US and EU regulations and quality standards applicable to antibody-based therapeutics and antibody-drug conjugates</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Strong attention to detail and problem-solving skills, with excellent project management skills</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Proven experience handling confidential and sensitive information with the ability to exercise discretion and show good judgment; honesty, integrity, and trust building behaviors in all dealings is essential and required</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Excellent customer-service orientation, high degree of professionalism, and the ability to work with limited direction</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Self-motivated, with initiative and the ability to take ownership of, and follow through with specific tasks</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">• Ability to multi-task and shift priorities quickly while working under tight deadlines</span></span></p> <p> </p> <p><strong><span style="font-family: verdana, geneva"><span style="font-size: 12px">Why Work for Us?</span></span></strong></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at www.zymeworks.com. </span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></span></p> <p><span style="font-family: verdana, geneva"><span style="font-size: 12px"><span style="color: #ffffff">#L1-JD1</span></span></span></p> Jun 27th, 2019 03:05PM Jun 27th, 2019 03:05PM Zymeworks
tsx:zyme zymeworks.bamboohr.com zymeworks.bamboohr.com Jun 27th, 2019 12:00AM Manager, Office Services Open Business Operations Permanent - Full Time Seattle Washington USA Apr 26th, 2019 12:00AM <p><span style="font-size: 14px">Zymeworks is a clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics.  Zymeworks’ suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.</span></p> <p><span style="font-size: 14px">Zymeworks is seeking a highly-motivated professional who is looking to grow their career with our company. </span></p> <p><span style="font-size: 14px">This position will report to the Senior Manager, Business Operations and will be based in Seattle, WA.</span></p> <p><span style="font-size: 14px"> </span></p> <p><span style="font-size: 14px"><b>Key Responsibilities:</b></span></p> <p><span style="font-size: 14px">• Manages and coordinates the efficient operations of the Zymeworks Biopharmaceuticals Inc. Office Services function, developing and executing on plans to improve daily administrative operations and ensuring maximum productivity, operational excellence and efficiency. </span></p> <p><span style="font-size: 14px">• Ensures that office operations between Zymeworks Inc. and Zymeworks Biopharmaceuticals are streamlined by following the Office Manager Operations Manual and working closely with Manager, Office Services of Zymeworks Inc.</span></p> <p><span style="font-size: 14px">• Manages direct report(s). Monitors performance, encourages growth and facilitates the development of team members’ skills through training, mentorship opportunities and sharing of knowledge. Ensures adequate coverage for essential services adjusting for absenses; monitors and establishes standards of work performance; organizes, schedules, assigns and reviews work—providing direction and technical guidance. Provides back-up relief for Seattle Office Services personnel, as necessary. </span></p> <p><span style="font-size: 14px">• Serves as a point of contact for internal office services inquiries. Develops, promotes and maintains effective communication, and positive working relationships in all internal and external interactions. Exercises considerable judgement when answering inquiries, conveying information, solving problems and directing people to the proper person or department for resolution of issues. </span></p> <p><span style="font-size: 14px">• Manages day-to-day operations of Seattle branch(es) including:</span></p> <p><span style="font-size: 14px">o Oversee the ordering of office supplies, stationary and lunchroom consumables.</span></p> <p><span style="font-size: 14px">o Ensure shared office spaces (ex. meeting rooms) are maintained in a clean and user friendly state.</span></p> <p><span style="font-size: 14px">o Organizes and supervises, as necessary, furniture and catering vendors, office janitorial services, off-site storage, building managers etc. as required.</span></p> <p><span style="font-size: 14px">o Manages, monitors and maintains employee services relating to transit passes, parking, and access cards.</span></p> <p><span style="font-size: 14px">o Tracks, analyses and proposes changes to seating arrangements to HR as required.</span></p> <p><span style="font-size: 14px">o Ensures facilities are maintained to a high standard of finish and arranges for repairs as required.</span></p> <p><span style="font-size: 14px">• Project manages Seattle-based corporate events and team building activities ensuring events are delivered efficiently, effectively and within budget. Develops Seattle based Social Committee and participates in corporate social committee when relevant,  liaises with key stakeholders/vendors, completes site inspections and manages all components of event ensuring activities are executed professionally and proficiently. Solicits formal feedback from participants and incorporates recommendations, as appropriate, in future events to help ensure excellent employee engagement and quality delivery. </span></p> <p><span style="font-size: 14px">• Contributes Seattle based office expenses to the annual facilities’ budget. Projects funds needed for office equipment, materials, supplies, corporate events, renovations and general office services projects. </span></p> <p><span style="font-size: 14px">•  Provides coordination and administrative support for ad hoc projects as requested, conducts research, compiles data and prepares special reports and other materials as requested. </span></p> <p><span style="font-size: 14px">• Manages the execution of all Seattle office renovations and upkeep from start to finish. As required, participates on project teams formed to address special projects including office moves and build-out of new facilities. </span></p> <p><span style="font-size: 14px">• Reviews, evaluates, develops and recommends procedures to improve operational efficiency of the Office Services department.</span></p> <p><span style="font-size: 14px">• Fosters effective and collaborative working relationships with fellow employees, management and external partners. </span></p> <p> </p> <p><span style="font-size: 14px"><b>Education and Experience:</b></span></p> <p><span style="font-size: 14px">University degree and a minimum 5 to 7 years years’ experience or an equivalent combination of education and experience. </span></p> <p> </p> <p><span style="font-size: 14px"><b>Skills and Abilities:</b></span></p> <p><span style="font-size: 14px">• Proven interpersonal skills with the ability to work collaboratively as a member of a team and to establish and maintain effective working relationships with employees, management and external associates.</span></p> <p><span style="font-size: 14px">• Strong organizational skills and the ability to work effectively in a high paced, fast changing environment. Results-oriented.</span></p> <p><span style="font-size: 14px">• Ability to supervise, train and motivate staff effectively and to promote a positive and respectful work environment. Previous experience monitoring performance and providing feedback.</span></p> <p><span style="font-size: 14px">• Excellent customer service skills with a proactive, problem solving approach. Ability to function professionally and pleasantly during periods of high stress.</span></p> <p><span style="font-size: 14px">• Strong computer skills and proficiency in MS Office.</span></p> <p> </p> <p><span style="font-size: 14px"><strong style="font-family: 'Source Sans Pro', arial, verdana, sans-serif">Why Work for Us?</strong></span><span style="font-size: 14px"> </span></p> <p><span style="font-size: 14px">Zymeworks’ employees are passionate, engaged and extremely motivated to succeed.  We are excited by the cutting-edge science and technology, the endless possibilities this union holds and the sheer opportunity to be a part of something big.  To learn more about Zymeworks Inc. and our current openings, please visit our website at www.zymeworks.com. </span></p> <p><span style="font-size: 14px">We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.</span></p> Jun 27th, 2019 03:05PM Jun 27th, 2019 03:05PM Zymeworks

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