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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 Date Added Date Updated Ticker Sector Ticker Industry
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Senior Manager, Quality Assurance Open Science Center Campus San Diego CA USA Jan 24th, 2019 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. Pacira BioSciences currently has an opening for a Senior Manager, Quality Assurance.

 

The purpose of this position is to provide organizational management and leadership to the Quality Assurance group and to ensure the cGMP compliance of the organization.

 

  • Responsible for ensuring the review, facilitation and timely closure of all Quality Events (QE).  Provide QA input and approvals to QE as needed. Ensure all QE’s are complaint and meet Pacira standards. 

  • Provide supervision to Quality Engineer.

  • Propose and approve CAPAs. 

  • Proactively participate and direct investigations as needed. Ensure investigations are thorough and determine root cause and product impact.

  • Develop department plans and strategies to ensure company goals are met.

  • Provide solutions to GMP related problems that are both compliant and are in alignment with Pacira standards and goals.

  • Develop and implement strategies to to improve group efficiencies and productivity. 

  • As needed, identify compliance gaps and proactively take steps to remediate.

  • As needed, review and approve  Standard Operating Procedures (SOPs), Change Controls, Validation Protocols/Reports, Batch Records and Engineering Drawings, ensuring internal and external standards are met.

  • Take leadership role as needed for all on-site inspections by regulatory agencies and partners.

  • Assist in the review of documents and data submitted in or in support of regulatory submissions.

  • Assist in the writing of Annual Product Reviews.

  • Other duties as assigned by Quality management.

The qualified candidate will possess the following:

  • Must have experience in an aseptic manufacturing environment. 

  • Ten (10) years of relevant Pharmaceutical Industry experience. 

  • BS degree in Chemistry/Biology or equivalent experience. 

  • Supervisory experience a plus.

  • Must have a strong understanding of Quality Systems and US and EU GXPs.

  • Ability to conceptualize, analyze, plan, organize and lead cross-functional projects.

  • Ability to manage multiple responsibilities with a high degree of self-motivation.

  • Strong communication, presentation, interpersonal, and organizational skills.

  • Proficiency in Microsoft Excel, PowerPoint, SharePoint, Project, Word and Adobe Acrobat applications.

  • Flexibility to work varying schedules to support occasional weekend, holiday and off shift work hours.

 

 

**No relocation assistance will be provided

 

Equal Opportunity Employer/Veterans/Disabled

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Associate Director, Regulatory Affairs CMC Open Science Center Campus San Diego CA USA Mar 21st, 2019 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. Pacira BioSciences currently has an opening for a Associate Director, Regulatory CMC

 

This position  provides regulatory expertise and leads regulatory projects for the Pacira Pharmaceuticals regulatory team.
 
Coordinate, write and review CMC sections for regulatory submission to US and international health agencies in the areas of new drug development, marketing applications, life-cycle management submissions, formal meeting briefing package.

  • Ensure conformance to commitments made with various health agencies (e.g., IND/NDA/MAA commitments).
  • Assist in developing regulatory strategies; identify and implement appropriate submission strategies for assigned projects. Provide input for product labeling, CMC changes and clinical projects.
  • Coordinate the submissions and ensure regulatory submissions are of high quality and submitted in a timely manner; review submissions for accuracy, completeness, and compliance with applicable regulatory requirements and internal procedures.
  • Participate in Regulatory interaction and presentations to Regulatory Health Authorities, customers and partners.
  • Monitor and maintain awareness of regulatory environment assessing impact to business, interpret and disseminate information to affected departments.
  • Other duties as assigned.

 

The qualified individual will possess the following:

 

Bachelor degree in life science from an accredited college or university

  • Minimum 8 years progressively responsible experience in Regulatory Affairs in the U.S. pharmaceutical industry
     
  • Demonstrated strong understanding of the U.S. and EU Regulatory requirements.

  • Proven ability to interpret and apply regulations to specific projects (FDA and ICH or other regulatory agency guidance requirements).

  • Excellent written and verbal  English communication skills

  • Demonstrated excellent organizational skills

  • Proven  negotiation skills.

  • Proven ability to manage multiple projects, set priorities and meet deadlines.

  • Excellent skill level in MS Office including Word, Excel and Outlook.

 

Equal Opportunity Employer/Veterans/Disabled

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Sr. Project Manager - Engineering Open Science Center Campus San Diego CA USA May 20th, 2019 12:00AM

At Pacira Pharmaceuticals, controlling postsurgical pain is the key to improving patient outcomes. Our in-depth knowledge of the needs of the postsurgical pain market, coupled with our passion for delivering improved patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. Pacira Pharmaceuticals currently has an opening for a Sr. Project Manager – Engineering.

Provides project management and engineering services to Manufacturing, Product Development, Facilities, and other partner groups.  Responsible for full project lifecycle development and managing projects on schedule and within budget while engaging customers and owners across multiple functions.  Key contributor to the development of PMO standards.

·         Experience in the design, construction, commissioning, and operation of:
o    Pharmaceutical-Biologics Manufacturing Systems: Chemical Synthesis, Fermentation/Cell Culture, Purification, Media/Buffer Preparation Operations, or Fill-Finish Operations.
o    Pharmaceutical-Biologics Manufacturing Support Systems: Clean Steam, Water-For-Injection, Clean-In-Place (CIP), Steam-In-Place (SIP), and Component Preparation.
o    Industrial Manufacturing Facility Systems: Plant Steam, Refrigerated/Chilled Water, Compressed Air, Process Gases (O2, N2, CO2), and Reverse Osmosis/Deionized (RO/DI) Water.
·         Full responsibility over effective management through full program and project management lifecycle.
·         Define and manage project/initiative scopes, execution resources (i.e. people, funds), timelines/schedules as well as indirect impacts on areas and/or partner groups.
·         Author and implement project management process guidance documents.
·         Manage the design, procurement, installation, start-up, and commissioning of pharmaceutical manufacturing facility systems and equipment.
·         Verify and/or execute Factory Acceptance Test (FAT), Site Acceptance Test (SAT), and/or commissioning protocols for pharmaceutical systems and equipment.
·         Assist Quality Assurance and/or Validation personnel during the execution of Installation-Operational Qualification (IOQ) protocols for pharmaceutical systems and equipment.
·         Work with and mentor junior project managers in developing new skills and career paths.


The qualified candidate will possess the following:

·         BS in Chemical Engineering, Mechanical Engineering or Manufacturing Engineering with 8-10+ years OR;
·         MS with 6-8+ years’ experience OR;
·         A minimum of 5 years overall direct experience with process and project engineering in pharmaceutical/biotech manufacturing.
·         A minimum of 10 years direct experience in project management and planning with 5 years of GMP related project experience.
·         PMP Certification preferred.
·         Application of PMI principles required.
·         Development and/or management of a PMO preferred.
·         Experience working with aseptic emulsion and/or filling equipment preferred.
·         Operational Excellence experience is a plus.
·         Experience developing and managing to corporate project management guidelines.
·         Strong organizational and teamwork skills.
·         Ability to influence individuals without having direct authority over them.
·         Creative problem solving skills.
·         Excellent written and oral communication skills are a must.
·         Advanced schedule management in Microsoft Project a plus (resource loaded Gantt, critical path/chain).
·         PC literacy required (Microsoft suite).
·         Must be able to read and interpret engineering and CAD documents.
·         Travel may be required (5-20%).

**No relocation assistance will be provided

Equal Opportunity Employer/Veterans/Disabled


Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Sr. Manufacturing Technician Open Science Center Campus San Diego CA USA Jun 27th, 2019 12:00AM

At Pacira Pharmaceuticals, controlling postsurgical pain is the key to improving patient outcomes. Our in-depth knowledge of the needs of the postsurgical pain market, coupled with our passion for delivering improved patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. Pacira Pharmaceuticals currently has an opening for a Sr. Manufacturing Technician.

 

The purpose of this position is to perform tasks and operations in either the bulk manufacturing or filling operations required in the preparation for and sterile production of liquid injectable, sustained release pharmaceutical products under cGMP regulations.

 

·         Bulk Manufacturing: Perform operations in CIP, SIP, and solution prep, take responsibility for set-up and preparation of the area for bulk manufacturing, utilize automated control systems, and other routine tasks

·         Filling Operation: Prep parts, run the vial washer/depyrogenation tunnel, autoclave, capping machine, tray loader, support the filling line, aseptic gown qualify, maintain aseptic qualification, inspect finished product

·         Understands critical process parameters and steps of activities sufficiently to act as a trainer for new employees

·         Complete GMP documentation (Batch Records, Forms, Charts, Data Entry )

·         Read, comprehend, and adhere to standard operating procedures (SOPs)

·         Participate in development and production of pipeline products

·         Author or assist in drafting and revising of departmental procedures and practices

·         Identify and communicate floor observations to supervisory staff

·         High level of proficiency with process equipment and automated control systems with the ability to troubleshoot, escalate issues and determine corrections

·         Organizational skills and an ability to perform assignments with a high degree of independence

·         Proficient and fully trained in cleanroom gowning and cleanroom practices

·         Participate in departmental aseptic process simulation (APS) qualification requirements

·         Assist in maintaining the production areas and records in a cGMP state at all times

 

 

 

Qualifications, Education, and Experience:

·         A minimum of 5 years of industry experience in the pharmaceutical or a closely-related industry required. However, exceptions may be made based on relevant educational degree.

·         A high school diploma/GED is required. Relevant experience may be substituted for diploma/GED requirement.

·         Bachelor’s degree from an accredited college/university may be substituted for industry experience.

·         Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

·         The ability and willingness to work as a member of a team, good interpersonal skills

·         Ability to work with minimal direct supervision and is self-driven to meet the schedule

·         Must have good attention to detail, documentation skills, and the ability to follow written procedures in a GMP environment

·         Must possess strong written and verbal English communication skills

·         Must have strong organizational skills and the ability to multi-task

·         Ability to operate in a cleanroom environment

·         Must understand and be proficient with basic arithmetic calculations, including calculating elapsed time and ratio calculations

·         Computer proficiency, including knowledge of Microsoft Word, Outlook, and Excel applications is required

·         Ability to accommodate production requirements that may occasionally require 50+ hour workweeks, including extended day hours and weekends

 

**No relocation assistance will be provided

 

Equal Opportunity Employer/Veterans/Disabled


Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Associate Account Manager - Atlanta Open Remote - Atlanta, GA Atlanta GA USA Dec 13th, 2018 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. Pacira Biosciences currently has an opening for an Associate Account Manager.

 

The Associate Account Manager (AAM) is responsible for supporting the positioning and selling of EXPAREL® and Pacira solutions within assigned territory. This includes the pharmacological & technical (Package Insert & functions, benefits) knowledge and sales of EXPAREL value proposition . The Associate AM will work with the Account Manager and Regional Director to develop a sound business plan that will lead to exceeding defined sales revenues for said territory. The Associate AM will utilize product knowledge, relevant hospital relationships, and business acumen skills and execute strategy to meet and exceed sales objectives of our flagship product EXPAREL®.

 

 

  • Identify target markets in accordance with organizational strategy utilizing familiarity with hospital operations and existing reporting, tools and dashboards.

  • Ensure that corporate revenue objectives are exceeded within a specified geography

  • Work with surgeons ,anesthesiologists,  health care providers and pharmacy; focused on pain management  to ensure that EXPAREL® is adopted within an account and geography

  • Utilize VEEVA to demonstrate proficiency in Account planning, forecasting, data analysis

  • Develop and maintain expertise of EXPAREL®

  • Work cross functionally with J&J counterparts to deliver customer adoption and proper utilization of EXPAREL

  • Effective time management skills to increase sales productivity and tactical implementation of sales activities to achieve business objectives and establish long-term value proposition of EXPAREL.

  • Actively participate with Account Manager and  Region Director in the strategic and tactical planning process

  • Update and document sales account information via software system (VEEVA)

  • Demonstrate expertise and knowledge of the conversion process within a hospital

  • Develop and execute sales and retention strategies for target markets and customers

  • Complete face-to-face sales meetings with physicians, schedulers, practice managers, and medical staff in hospitals to ensure understanding, as well as to close business, ensuring that obstacles are identified and minimized.

  • Effectively manage territory, conducting office visits to include: Education on services offered, enhancement and new advances.

  • Communicating opportunities, market trends, and issues to appropriate management/staff in a timely manner

  • Prepare and present opportunities, market trends, and challenges to appropriate leadership/staff in a timely manner and on a regular basis, gaining support and commitment as needed.

  • Manage  expense budgets in a timely manner

  • Keeping up to date with latest clinical data supplied by the company and interpreting, presenting and discussing this data with health care professionals during presentations.

 

 

 

The qualified individual will possess the following:     

 

 Bachelor’s degree from accredited college or university, Science or Business major required GPA minimum 3.2


1-2 years of direct selling experience to hospitals and healthcare professionals in the pharmaceutical, biotech, device or health care industry preferred. Will consider relevant business internship experience.

  • Excellent written and oral English communication skills,

  • Strong demonstrated presentation skills.

  • Must be able to timely and accurately complete Hospital Credentialing requirements to gain access to their facilities

  • Able to travel extensively; valid driver’s license in the state in which you reside; reliable transportation.

  • Must live in your designated geographic territory.

  • Must have valid driver’s license in the state in which you reside.

  • Knowledge of key industry business drivers, emerging medical trends, and performance metrics, and ability to leverage that knowledge to inform strategy.

  • Strong communication, interpersonal, collaborative, and analytical skills with a customer focus; must be able to foster and maintain sound working relationships.

  • Independently motivated and driven to achieve high goals and seek continuous improvement in knowledge and skills.

  • Competencies for sales efficiency and effectiveness; discipline in goal setting, prospecting, networking, territory management, and time management. Skills in account management, needs assessment, value propositioning, handling objections and gaining agreement.

  • Skills to employ technologies effectively and proficiency (MS office suite, relevant mobile technology and web-based applications.)

  • Demonstrated  successful working relationships with surgeons, anesthesiologists and Hospital Pharmacy in the territory

  • Overnight travel will be required, ability to cover geographic territory; including corporate meetings. Able to travel overnight and locally up to 90% of the time.

     

     

    Equal Opportunity Employer/Veterans/Disabled

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Assembler - Temp to Perm - Swing Shift Open Fremont Office Fremont CA USA May 7th, 2019 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. We currently have multiple opportunities available for Assemblers (Swing Shift) in our CryoTech division based in Fremont, CA.

The Assembler will support production builds in both the clean room environment and outside the clean room environment for building product.  Assemble, test, clinical and market released product, following defined instructions.

·         Complete work projects assigned in a timely manner and document work performed.

·         Work with department supervisor, lead, engineers and other departments to improve productivity.

·         Assemble products under the direction of lead, supervisor and/or manufacturing engineering and complete routers/travelers for each work order.

·         Learn and apply standard test methods and processes.

·         Test production devices following standard test procedures.

·         Assemble cartridges and smart tips.

·         Build and Refurbish hand pieces

·         Cross training in other areas of manufacturing.


The qualified candidate will possess the following:


·         High school diploma and 2 years of related experience, ideally in a manufacturing and/or medical device environment or equivalent combination of education and experience.

·         A candidate with gluing adhesive and/or catheter experience would be preferred.

·         Ability to read and follow instructions and documents such as safety rules, operating and maintenance instructions, and procedure manuals.

·         Experience with Microsoft Office (Word, Excel, Outlook).

·         Ability to communicate effectively through oral and written communications and work with others collaboratively.

·         Ability to use a microscope, and small hand tools such as screwdriver, pliers, tweezers.

·         Ability to perform repetitive tasks.

·         Work under limited supervision  

·         Solder skills a plus

 

Equal Opportunity Employer/Veterans/Disabled

 

 

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Marketing Associate - Digital Marketing Open Headquarters Parsippany NJ USA Jan 19th, 2019 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.

 

The Marketing Associate - Digital Marketing is responsible for collaborating across the Pacira organization and with alliance partners (such as Johnson & Johnson) teams to coordinate and execute marketing programs and strategy, training materials for internal and external customers, professional engagements and education, and society meetings.

  • Develop, manage and optimize content across digital (i.e, EXPAREL.com website, Search, Email, Social media) platforms in support of the Marketing and Commercial organizations’ strategic priorities  

    • Drive analytics reporting and lead optimization initiatives

    • Implement specialty-focused content on EXPAREL.com (“online learning”) in coordination with Marketing and Commercial leadership and Medical and Scientific communication teams

  • Liaise with digital vendors and agency to continually optimize paid search, SEO initiatives and other key drivers to grow and enhance EXPAREL business and education

  • Identify growth marketing opportunities and other customer acquisition (patient and HCP) initiatives as part of ongoing improvement and annual strategic plan

  • Support planning, process management and execution of surgical case reports and videos (i.e., partnering with Marketing vertical leads to engage with key opinion and thought leaders, managing video script and content approval process, and coordinating launch of materials to internal and external customers)

  • Interface with medical/legal/regulatory review team to drive operational efficiency of marketing/commercial team

  • Develop and maintain project management tools outlining active work streams, monitoring status and immediate next steps. Build team processes to improve coordination and collaboration.

  • Communicate with stakeholders to ensure necessary input is received and issues are triaged to appropriate individuals.

  • Create and maintain performance metrics, reports and dashboards as needed

  • Develop and refine  key executive presentations and reports, as required

The qualified individual will possess the following:

  • Bachelor’s degree in Business, Marketing or related field from accredited college or university

  • Minimum 3 years’ experience in marketing or project coordination, preferably in a business development or pharmaceutical/biotech/medical devices environment.

  • Minimum 2 years’ experience in pharmaceutical/biotech/medical devices Product Management, Marketing or Business Development, preferably with a product launch.

  • Agency experience or prior experience managing agency partners a plus

  • Proven ability to communicate effectively with all levels of the organization (including C-suite) as well as with external constituents including KOLs and business partners.

  • Self-starter

  • Demonstrated skills in Pharmaceutical product launch planning and execution

  • Demonstrated analytic skills

  • Proven ability to manage complex projects to completion – project and timeline management

  • Proven ability to manage multiple tasks, set priorities and meet deadlines

  • Demonstrated ability to work successfully with minimal supervision and to collaborate well with team members across functions

  • Excellent Microsoft Office skills including Word, Excel and PowerPoint

  • Excellent oral and written English communication skills

  • Ability to travel up to 30%  

  • Google Analytics and AdWords experience a plus  

**No relocation assistance will be provided 

Equal Opportunity Employer/Veterans/Disabled

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Director, Tax Open Headquarters Parsippany NJ USA Feb 21st, 2019 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.

The Senior Director, Tax will oversee all aspects of corporate income tax, sales and use tax, real and personal property tax, VAT, and annual reports/ franchise tax.  Manage and optimize key processes such as income tax accounting, compliance, and transfer pricing. Lead the development and implementation of tax planning strategies and provide technical assistance on various tax issues. Partner with Company management and third party service providers to ensure policies and processes mitigate risk and proactively identify savings opportunities.

  • Oversee the preparation, review, and timely and accurate submission of all US and foreign corporate income tax returns reports, and payments including R&E credit and 5471s. 

  • Prepare timely and accurate global tax provisions, tax-related account reconciliations, return-to-provision, and tax footnote for 10K/10Q filings.

  • Prepare transfer pricing documentation in accordance with IRS regulations.

  • Execute tax strategies based on company goal and objectives.

  • Monitor tax law changes and impact on returns and provision.

  • Direct, revise, and design tax processes to ensure efficient operations of the tax function.

  • Manage tax-related special projects such as intercompany transactions and contracts, due diligence, formation of new legal entities and/or branches, capacity expansion, etc.

  • Supervise and collaborate with tax contractors and consultants.

  • Oversee and/or prepare indirect tax calculations and filings including franchise taxes, VAT, sales & use tax, and San Diego personal property taxes.

  • Effectively manage all tax audits.

  • Evaluate ASC 740 (FIN 48) for uncertain tax positions.

  • Develop tax forecasts to allow for tax planning and long-range projections of effective tax rates.

  • Anticipate internal and external tax compliance challenges or regulatory issues, research implications to the business, and provide recommendations to management.

  • Review tax implications of potential business development or in-licensing opportunities.

  • Organize and ensure SOX 404 documentation reflects current practices and procedures for tax processes.  

 

The qualified candidate will possess the following:

    • 10+ years of corporate tax experience.

    • Bachelor’s degree in Accounting, Finance or related degree.

    • Advanced credentials (e.g. Masters in Taxation, MBA and/or CPA).

    • Strong technical knowledge of complex tax issues.

    • High level of proficiency in Excel required.

    • Excellent verbal and written communication, presentation, and management skills.

    • Problem solving skills evidenced by demonstrated results in past positions.

    • Strong attention to detail. Must be able to manage several tasks concurrently.

    • General knowledge of GAAP/SOX and an understanding of internal accounting controls.

    • Highly motivated, results focused, fast-acting, decisive, and accountable. 

 

 

Equal Opportunity Employer/Veterans/Disabled

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Project Manager, Medical Operations Open Headquarters Parsippany NJ USA Feb 27th, 2019 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.

The Medical Operations Project Manager serves as a liaison among medical teams. He/she fully understands the strategic and tactical plans set for the medical departments as well as standard procedures and ensures adherence to these procedures. The Project Manager assures smooth work flow by scheduling events, defining timelines, establishing priorities, and following up with each team member through all phases of each individual tactic/project to ensure each project is completed on time and within budget.

  • Manage assigned projects, including but not limited to planning, executing and closing to ensure the objectives of the projects are met.

  • Champions, organizes, and manages medical review submissions per guidelines process and maintains records on the appropriate portal for all medical assets.

  • Creates project planning schedules for every departmental project.

  • Updates, maintains, and distributes status reports. Partners with the Business Leads, to keep status and next steps completely up-to-date for all projects

  • Upholds quality control standards and practices.

  • Communicates changes, revisions, and approvals to the appropriate members of the team and potential vendors as needed for projects

  • Participates in monthly financial meetings and maintains proper financial records. Contribute to budgeting and forecasting.

  • Establishes objectives, priorities, and organize a practical work schedule, ensuring effectiveness by following through on each print job to each stage of completion

  • Ensures efficient flow of activities and works with cross company operations team members to gain alignment and develop tools, update processes as needed. This includes the development of templates, slides, reports and smartsheets to accurately capture key performance indicators.

The qualified candidate will possess the following:

  • B.A. or B.S. in marketing, communications or biology preferred

  • Minimum of 3 years of health sciences experience is required; pharmaceutical industry or related experience is preferred; work in the areas of operations, and/or project management a plus.

  • Formal project management training (e.g. PMP) a plus.

  • Strong computer skills, including Microsoft Word, Excel, Power Point and Project Management software.

  • Demonstrated project management skills (full project life cycle) with the ability to work on multiple projects simultaneously with troubleshooting/problem solving abilities.

  • Sound organizational skills.

  • Excellent verbal and written English communications skills including ability to communicate about technical data.

  • Strong computer skills, including Microsoft Word, Excel, Power Point and Project Management software.

  • Demonstrated ability to work well across teams and functions with the ability to work well in a matrix environment.

  • Proven ability to work effectively on a team in an entrepreneurial environment.

Equal Opportunity Employer/Veterans/Disabled

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology
nasdaq:pcrx pacira.csod.com pacira.csod.com Jul 17th, 2019 12:00AM Clinical Trial Project Coordinator Open Headquarters Parsippany NJ USA Feb 28th, 2019 12:00AM

Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.  

The Clinical Project Coordinator serves as a liaison among medical teams. He/she fully understands the tactical plans set for the medical departments as well as standard procedures and ensures adherence to these procedures. The Project Coordinator assures smooth work flow by scheduling events, establishing priorities, and following up with each team member through all phases of each individual tactic/project to ensure each project is completed on time and within budget

 

  • Champions, organizes, and manages clinical submissions per review guidelines and maintains records on the appropriate portal for all clinical assets.

  • Creates time and events schedules for every clinical project.

  • Updates, maintains, and distributes status reports, keeping them up-to-date at all times. Partners with the Business Leads, to keep status and next steps completely up-to-date for all projects

  • Upholds quality control standards and practices.

  • Participates in monthly financial status meetings and maintains proper financial records.

  • Runs monthly budget vs. actual reports and distributes them to the team

  • Establishes objectives, priorities, and organize a practical work schedule, ensuring effectiveness by following through on each print job to each stage of completion

  • Ensures efficient flow of activities and works with cross company operations team members to gain alignment and develop tools, update processes as needed. This includes the development of templates, slides, reports and smartsheets to accurately capture key performance indicators.

The qualified candidate will possess the following:

  • B.A. or B.S. with a minimum of 2-3 years of pharmaceutical, or project management experience

  • Strong computer skills, including Microsoft Word, Excel, Power Point and Project Management software.

  • Formal project management training (e.g. PMP) a plus

  • Demonstrated project management skills (full project life cycle) with the ability to work on multiple projects simultaneously with troubleshooting/problem solving abilities.

  • Sound organizational skills.

  • Excellent verbal and written English communications skills including ability to communicate about technical data.

  • Strong computer skills, including Microsoft Word, Excel, Power Point and Project Management software.

  • Demonstrated ability to work well across teams and functions with the ability to work well in a matrix environment.

  • Proven ability to work effectively on a team in an entrepreneurial environment.

           

Equal Opportunity Employer/Veterans/Disabled



                                                                       

Jul 17th, 2019 12:13AM Jul 17th, 2019 12:13AM Health Care Pharmaceuticals & Biotechnology

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Visualize data for quick insights

Create custom keyword-based word clouds, charts, and advanced visualizations to quickly analyze the data.

Map competitor locations

Analyze competitor presence and growth over time by overlaying store locations with the Nearby Competitor feature.