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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Mechanical Engineer
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Open
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Engineering
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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Feb 10th, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and wellbeing of people around the globe with well-known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology.</div><div> </div><div class="BodyCopy" align="left">We're looking for an experienced mechanical engineer that can design, build, and test sophisticated and highly reliable electromechanical subassemblies. You will work with R & D, Instrument Systems, Quality Control, Manufacturing, and Contract Manufacturers to develop hardware and manufacturing solutions for new and on market products. The position is focused on mechanical and electro-mechanical assembly and component life-cycle design. Looking for an engineer with a solid theoretical and practical background in mechanical engineering, who can comprehend form, fit, and function replacement alternatives to yield improved product performance. Interacting with Instrument Systems to drive practical and robust designs, implementing Design for Manufacturability (DFM), design of manufacturing equipment, processes, and QC inspection methods.</div><div><strong> </strong></div><div><strong>ESSENTIAL FUNCTIONS:<br /><br /></strong></div><ul><li>Provide leadership in DFA/DFM to product development teams for manufacture of IVD instruments.</li><li>As a product development team member, you will participate in the product development process by designing, assembling and testing prototype systems, and release to manufacturing.</li><li>Own engineering responsibility for electro-mechanical subsystem after first customer shipment.</li><li>Lead design transfers that result in processes that are robust, technically feasible, and can be effectively scaled for high volume manufacturing.</li><li>Perform analysis on field returns, define problem, indentify root cause, recomment and implement solutions.</li><li>Generate material specifications and coordinate with Supply Chain to ensure that new designs incorporate raw materials that can be consistently procured at optimal cost.</li><li>Maintain Design Control and project documentation in accordance with Quidel and external regulatory requirements.</li></ul><br/><br/><div><strong>Education and Experience:</strong></div><ul><li>B.S./M.S. in Mechanical Engineering or equivalent</li><li>4-7+ years of relevant experience in electro-mechanical system and subsystem design, NPI, and manufacturing</li><li>3+ years of experience in SolidWorks</li></ul><div> </div><div><strong>Knowledge / Skills:<br /></strong></div><ul><li>Skilled in mechanical design & Design for Manufacturability (DFM)</li><li>Ability to generate working drawings to support component fabrication</li><li>Knowledge of manufacturing processes and equipment</li><li>Must be proactive and require minimum supervision</li></ul><ul><li>Strong analytical and problem-solving skills</li><li>Good organizational skills, and the ability to manage multiple tasks</li><li>Ability to work within cross-functional teams</li><li>Strong communication skills, written and verbal</li><li>Knowledge in project management</li></ul><ul><li>Skilled in problem-solving and troubleshooting</li><li>Knowledge in managing technical projects with external contractors</li></ul><div> </div><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div><strong> </strong></div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.</strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Senior Quality Engineer
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Open
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Engineering
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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May 4th, 2020 12:00AM
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<div><div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and well being of people around the globe with well known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology. </div><div> </div><div>SUMMARY OF POSITION:</div><div> </div><div>This position is responsible for the successful transfer of new products from R&D into manufacturing which requires the ability to develop appropriate acceptance criteria for product transfer. The Sr. Quality Engineer, New Products ensures that quality tools such as Failure Mode and Effects Analysis (FMEA) and Manufacturing Control Plans are effectively determined and implemented prior to product transfer. The position acts as a key member of Quidel’s Validation Review Committee by evaluating changes to existing products, assessing the acceptance criteria, and ensuring no adverse impact on product performance. This role plays an integral part with Quidel’s product and process validation system and supports Quidel’s Technical Support and Marketing teams by providing technical assistance related to product expectations and other quality considerations. </div><div> </div><div>ESSENTIAL FUNCTIONS<strong>: </strong></div><ul><li><div>Ensure FMEAs for new and existing products are robust and complete. Continually review and update FMEAs as failure modes are identified<em> </em></div></li><li><div>Ensure the control points proposed through the design and development process are evaluated for adequacy as related to field performance and manufacturability</div></li><li><div>Support escalations related to stability study of new product launches and/or changes to existing product or regulations</div></li><li><div>Participate in Complaint Committee meetings and present investigation findings to peers and management </div></li><li><div>Represents the Quality Control department in evaluating readiness for product launch. </div></li><li><div>Perform statistical analysis of data from experiments and manufacturing process trend monitoring</div></li><li><div>Participate in New Product team meetings and Validation Review Committee meetings (VRC).</div></li><li><div>Support and lead complex root cause failure investigation and troubleshooting of customer complaints and product nonconformances within manufacturing</div></li><li><div>Monitor field complaint data to evaluate new product performance and the impact of changes</div></li></ul></div><div> </div><div><strong> </strong></div><br/><br/><div><span style="font-family: Calibri; font-size: medium;">Education and Experience</span></div><ul><li><div>B.S. in Engineering/Chemistry/Biology/Technical Discipline or equivalent combination of certification and work experience preferred</div></li><li><div>6-8 years’ experience in Quality and Manufacturing Systems in Medical Device and high-volume manufacturing environments required</div></li><li><div>Minimum 3 years’ experience in New Product introductions preferred</div></li><li>ASQ Quality Engineer Certification (CQE) preferred</li></ul><div>Knowledge/Skills</div><ul><li><div>Quality Engineering skills which includes FMEA, Control Plans, Acceptance criteria, Sampling Plans.</div></li><li><div>Strong technical aptitude and experience (preferably in engineering, chemistry, biology or other life sciences field) is a must.</div></li><li><div>Quality Tools – Problem Solving Methodologies/Process Capability / ISO 13485 / Design of Experiments.</div></li><li><div>Ability to communicate effectively with all levels of employees throughout the organization</div></li><li><div>Ability to develop and maintain strong working relationships with internal and external customers</div></li><li><div>proficient in Microsoft Office, statistical software programs, operating systems, voice and email, etc.</div></li><li><div>Ability to lead and facilitate a group of technical experts in root cause investigations </div></li><li><div>Knowledge of quality systems and regulations for medical device industry.</div></li><li><div>High level of technical writing ability and excellent communication skills are required</div></li><li><div>Advanced skills in statistical techniques and quality tools is required </div></li><li><div>Understanding of medical device Quality System Regulations (QSR) is required</div></li></ul><div> </div><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div> </div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. </strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Production Technician III
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Open
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Engineering
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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May 13th, 2020 12:00AM
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<div><div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and wellbeing of people around the globe with well-known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology.</div></div><div> </div><div>Quidel is searching for a Production Technician III to work at our manufacturing facility in the Sorrento Valley Area of San Diego. The purpose of this position is to schedule, perform, and oversee the maintenance, operation, and repair of production equipment. Taking ownership of assignments directed at improving total operating efficiency, minimizing equipment downtime and improving internal administrative processes are key elements for this role. The Production Technician II will also interacts heavily with other Production Technicians, Production Associates and internal team members such as Manufacturing Engineers, Quality, Production Managers and contract service providers. This role will be required to work on-call shifts as needed. Additional responsibilities include:</div><ul><li>Responding to trouble calls from Production Operators, providing assistance with equipment set-up, material change-out, line clearance, and basic operation.</li><li>Coordinating efforts with outside vendors and contract service providers to accomplish objectives.</li><li>Performing routine preventative maintenance on production equipment utilizing the MP2 system.</li><li>Troubleshooting and resolving complex mechanical issues with limited supervision and guidance.</li><li>Lifting and moving equipment in excess of 50 pounds.</li></ul><br/><br/><div><strong><span style="text-decoration: underline;">Education and Experience</span></strong><strong>:</strong></div><ul><li>High school diploma or equivalent is required. A technical degree or equivalent experience is preferred. </li><li>A minimum of 3-5 years’ experience working with production equipment and systems is required. A minimum of 5 years’ experience with electrical applications up to 480 volts is preferred.</li><li>Experience with hand and power tools and their associated safety procedures is required. Experience working in GMP/ISO 9000 manufacturing environment is preferred.</li><li>Experience working in high paced manufacturing environment</li></ul><div><strong><span style="text-decoration: underline;"> </span></strong></div><div><strong><span style="text-decoration: underline;">Knowledge/Skills</span></strong><strong>:</strong></div><ul><li>Knowledge of QSR/ISO 9001 is preferred.</li><li>Understanding and application of safety procedures</li><li>Strong abilities in the areas of communication, cooperation, interpersonal skills and documentation</li><li>Ability to prioritize multiple tasks and work independently.</li><li>Basic skills with machine lathe, mill and welding is preferred</li><li>Basic computer skills including, file management, MS Word, and preventative maintenance software</li><li>Ability to lift moderate to heavy equipment in excess of 50 pounds.</li></ul><div> </div><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div> </div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. </strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Equipment Engineer
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Open
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Engineering
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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Jun 12th, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and well being of people around the globe with well known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology. </div><div> </div><div>This role will support the cartridge engineering and manufacturing groups by sustaining existing production lines, developing new manufacturing processes, and specifying and procuring new manufacturing equipment.</div><div> </div><div>Responsibilities Include:</div><div><strong> </strong></div><ul><li>Directs Equipment Technicians to sustain existing production processes and troubleshooting, implements and maintain equipment maintenance schedules.</li><li>Supports the development and execution of IQ / OQ validations, special project plans, procedures and maintenance protocols for production equipment</li><li>Develops new equipment strategies and generates documentation and cost analysis to support procurement of capital equipment.</li><li>Generates equipment specifications, identifies equipment suppliers and supports equipment build activities including design reviews and project timelines. Installs and validates upgrades and new equipment, develops and conducts operator and maintenance training</li><li>Works with R&D and Engineering peers to develop and implement new MFG processes Develops QC support equipment. Performs related analysis and testing to support raw material and part compatibility.</li><li>Maintains and upgrades equipment safety systems to assure safe and ergonomic working environments.</li></ul><br/><br/><div ><strong>Education/Experience</strong></div><ul><li>HS Diploma required, BS degree preferred. </li><li>Minimum of 5 years’ experience, preferably in an automated manufacturing environment with specific experience in the following: Preventive Maintenance, Troubleshooting (mechanical, electrical distribution, electrical controls), PLC (hardware and software), machining, and welding.</li></ul><div ><strong>Knowledge/Skills</strong></div><ul><li>Electrical-Mechanical Theory & Application</li><li>Process and Assembly Automation</li><li>Pneumatics, Instrumentation, PLC and Machine Programming</li><li>Basic quality tools</li><li>Excellent written and documentation skills</li></ul><div >Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div > </div><div ><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. </strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Instrument Hardware Verification Engineer
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Open
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Instrument Systems
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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Jun 16th, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and well being of people around the globe with well known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology. </div><div> </div><div><div><strong>ESSENTIAL FUNCTIONS:</strong></div></div><ul><li><div>Conducts verification and validation of instrument electronics and mechanical hardware, including both testing to requirements and fault insertion testing</div></li><li><div>Designs and builds test jigs, fixtures, and data collection systems for fault insertion and design verification testing</div></li><li><div>Troubleshoots performance defects identified during testing and works with development engineers to resolve them</div></li><li><div>Develops hardware verification strategy for components, subsystems and systems including writing test protocols.</div></li><li><div>Maintains hardware verification and validation documentation in accordance with internal Quidel and external regulatory requirements as part of the design control process</div></li><li><div>Responsible for configuration management for instruments under test</div></li><li><div>Works with Instrument Systems personnel to evaluate new technologies and improvements to existing technologies as used within Quidel instrument products</div></li></ul><br/><br/><div><strong><span style="text-decoration: underline;">Education and Experience</span></strong><strong>:</strong></div><div><strong><br /></strong></div><ul><li><div>Bachelor’s Degree in Electrical Engineering, Mechanical Engineering, or related equivalent degree</div></li><li><div>5+ years of relevant experience in a medical device or consumer electronics environment</div></li></ul><div> </div><div><strong><span style="text-decoration: underline;">Knowledge/Skills</span></strong><strong>:</strong></div><div><strong> </strong></div><ul><li><div>Experience in electromechanical hardware development and test</div></li><li><div>Experience with outside testing houses or agencies to complete testing</div></li><li><div>Good organizational skills, and the ability to manage multiple tasks</div></li><li><div>Strong analytical and problem-solving skills</div></li><li><div>Knowledge of related quality systems regulations and processes preferred, e.g., ISO13485 and FDA 21 QSR 820</div></li><li><div>Application of electromechanical testing equipment, e.g., oscilloscope, thermocouples, voltmeters, environmental chambers, data loggers</div></li><li><div>Design and creation of hardware test jigs, including fault insertion, e.g., to demonstrate correct step loss detection, sensor failure</div></li><li><div>Ability to work within cross-functional teams</div></li><li><div>Strong communication skills, written and verbal</div></li><li><div>Must exhibit professionalism, confidence, maturity, desire to succeed, proactive and self-motivated</div></li><li><div>Appropriate office computer skills (e-mail, word processing, statistical, spreadsheet and graphing software)</div></li></ul><div><strong> </strong></div><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div> </div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. </strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Sr. Global Product Manager
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Open
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Marketing
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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Jun 16th, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and well being of people around the globe with well known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology. </div><div> </div><div>Leads and directs the Quidel global strategy, product portfolio/lifecycle management and global commercial efforts for an important product category (e.g., cardiology, infectious disease, toxicology). Manages and develops small number of direct reports on the global product team. Extensive matrix management of full range of cross-functional efforts supporting the products, services and other offerings in the product category. Collaborates with US and International commercial leaders to establish annual/long-term financial targets and to execute strategies and tactics to achieve them.</div><div> </div><div><strong>ESSENTIAL FUNCTIONS:</strong></div><div><strong> </strong></div><ul><li><div>Develop the high-level business strategies for the product category, products, related services and commercial approach</div></li><li><div>Lead product team and broader company efforts to gain/maintain a comprehensive understanding of the markets, market dynamics and other factors related to company success with current products, product improvements and new product introductions:</div><ul><li><div>Target markets/market segmentation</div></li><li><div>Customer needs/unmet needs</div></li><li><div>Current and future competitive landscape</div></li><li><div>Other factors impacting the market and related opportunities</div></li><li><div>Key success factors needed for commercial success</div></li><li><div>Quidel core competencies and capabilities</div></li></ul></li><li><div>Lead and manage the cross-functional efforts related to the entire category product portfolio:</div><ul><li><div>Identification of product improvements/new product opportunities and the development of the market requirements and key specifications for these products</div></li><li><div>Develop business cases to support company investment in product development</div></li><li><div>Play a key leadership role on the core teams working on the development of new products under the company’s “phased approach”</div></li><li><div>Develop and execute new product launch plans in concert with the Quidel commercial team leaders around the world to include, target markets/customer segments, product positioning, pricing, sales strategy, field training, awareness and educational programs, etc.</div></li><li><div>Identify and drive scientific study efforts needed to support commercial support of new and existing products.</div></li><li><div>Monitor company commercial performance in the product category. Work with commercial team leaders to refine/develop strategies and tactics to drive better performance. Work to assess company capabilities and drive improvements where needed.</div></li><li><div>Manage the products through the entire life cycle, replacing and/or sun-setting as is appropriate</div></li></ul></li><li><div>Work with commercial team leaders to establish annual/long term financial targets and to execute efforts to meet/exceed these targets</div></li><li><div>Champion and create awareness of the customer across the entire Quidel organization in order to motivate behaviors critical to quality products and strong customer service.</div></li><li><div>Recruit, manage and develop small team of direct reports</div></li><li><div>Carry out duties in compliance with established business policies.</div></li></ul><br/><br/><div><strong><span style="text-decoration: underline;">Education and Experience</span></strong><strong>:</strong></div><div><strong><br /></strong></div><ul><li><div>Bachelor’s degree required; MBA highly preferred</div></li><li><div>7+ years’ experience in marketing, product management or strategy solving complex commercial problems</div></li><li><div>At least 3 years in a leadership/senior manager capacity with direct supervision experience </div></li><li><div>Prefer experience in IVD industry and experience with a manufacturing company.</div></li></ul><div> </div><div><strong><span style="text-decoration: underline;">Knowledge/Skills</span></strong><strong>:</strong></div><div><strong> </strong></div><ul><li><div>Proven leadership demonstrated by the ability to establish strong relationships, motivate employees, influence stakeholders, and gain consensus on solutions</div></li><li><div>Ability to develop, motivate and develop team of high performing analysts and managers. Strong empowerment and delegation skills.</div></li><li><div>Strong and efficient analytical and problem-solving skills with the ability to produce meaningful analyses, insights and recommendations</div></li><li><div>In-depth understanding of the relevant market dynamics in target markets around the world</div></li><li><div>Ability to articulate vision and direction via solid interpersonal skills with ability to interact with all levels of employee groups and management</div></li><li><div>Skilled in developing effective presentations that effectively communicate ideas using graphs, charts, and other illustrative methods</div></li><li><div>Skilled in all aspects of business research (industry analysis, competitive benchmarking, VOC) and using framework driven analyses to efficiently deliver meaningful insights and gain consensus on recommendations</div></li></ul><div><strong> </strong></div><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div> </div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. </strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Senior IS Analyst
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Open
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Information Systems
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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Jun 18th, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and wellbeing of people around the globe with well-known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology.</div><div> </div><div>Quidel is known as a leader in medical device connectivity, introducing the Virena platform for disease surveillance in 2014. With over 15,000 instruments contributing key information to our Virena platform, we can assist healthcare professionals understand key public health trends in their local communities. However, Virena was just the beginning. Working within the IS Connected Solutions team, you can help take us to the next level of connected instruments. Join the loT revolution in medical technology with a proven industry leader.</div><div><strong> </strong></div><div><strong>ESSENTIAL FUNCTIONS:</strong><strong> </strong></div><ul><li>Provides functional support to internal customers and end users of IS System(S) and related business applications. Support includes training employees in using functionality of the system, troubleshooting system, and acting as a liaison between IS and functional business users.</li><li>Assist in improvement initiatives that support business objectives by gathering requirements and translating those into clear and accurate functional and technical specification documents, Researches alternatives and determines the best course of action to satisfy the user requirements</li><li>Design and document customizations pertaining to process changes</li><li>Develops testing and validation plans and supervises their execution and completion;</li><li>Carry out duties in compliance with established business policies including but not limited to the change management process.</li><li>Works with end users on post-project training, issue resolution and documentation to ensure a successful completion to the project;</li><li>Establishes a mechanism to measure and continuously improve the quality of key data used within the functional area.</li><li>Perform activities supporting any internal security, compliance and audit requirements.</li><li>Mentors team members as needed.</li></ul><br/><br/><div><strong>EDUCATION, SKILLS & EXPERIENCE:</strong> </div><ul><li>Bachelor’s degree required, Master’s degree preferred, in Computer Science or a Business-related field. Equivalent work experience may be substituted.</li><li>At least 10 years of experience working in a corporate IS/IT environment, with at least 6 years of business analysis experience on the platform or application in scope for the position, or equivalent operational experience within applicable business function</li><li>Possesses strong communications skills with the ability to represent highly complex topics to any level of the organization</li><li>Excellent customer service, interpersonal and presentation skills</li><li>Strong requirements analysis and documentation skills</li><li>Demonstrated planning and organizational skills including Agile methodology</li><li>Strong understanding of data management and administration principles</li><li>Knowledge of Sarbanes-Oxley 404 compliance requirements</li><li>Proficient with Microsoft Office </li></ul><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div><strong> </strong></div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.</strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Aug 13th, 2020 12:00AM
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Senior IS Analyst (Salesforce)
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Open
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Information Systems
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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Jun 29th, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and wellbeing of people around the globe with well-known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology.</div><div> </div><div>Organizational growth has created the need for a Sr. Salesforce Analyst to work closely with our various business teams to deliver enhanced capabilities and improved business processes on the expanding Salesforce platform. The Sr. Salesforce Analyst will work closely with functional business leaders and subject matter experts to identify, configure/develop and deploy new and enhanced business processes for this high-profile application. This position will perform a broad range of tasks which include research, analysis, design, configuration, coding, testing, maintenance, support, training, and implementation of business solutions within the Salesforce platform.</div><div> </div><div><strong>Essential Functions:</strong></div><ul><li>Work with business stakeholders to streamline processes and knowledge flows, leveraging Salesforce best practices</li><li>Analyze complex requirements; develop appropriate solutions using Salesforce functionality to support diverse business needs</li><li>Create and maintain process documentation, policies, configuration and help guides for users</li><li>Manage data import, data cleansing, deduplication, optimization, and data maintenance efforts</li><li>Support users reporting needs across Standard and Custom Objects</li><li>Manage environments and code deployments</li><li>Coordinate and support third party Apps (e.g. Conga, DocuSign, Social Studio) integration and upgrades</li><li>Use of analytics tools and business reporting</li><li>Partner with IT Security team to ensure system security and integrity</li></ul><br/><br/><div><strong>Education/Experience:</strong></div><ul><li>A Bachelor’s Degree in computer science/technology or related work experience</li><li>5+ years with the Salesforce platform that includes professional experience in Salesforce Applications configuration</li><li>Active Salesforce Admin or Salesforce Developer Certifications</li><li>Experience in healthcare or medical device industry preferred</li></ul><div><strong>Knowledge/Skills:</strong></div><ul><li>An understanding of Salesforce customizations (Apex classes and Triggers, VisualForce, Lightning Web Components) and configurations (Formulas, Workflows, Approval Processes, Custom objects and fields, sharing rules, page layouts, permission sets, reports and dashboards)</li><li>Creative and analytical thinker with strong problem-solving skills</li><li>Proficient with Salesforce Lightning</li><li>Proficient with Microsoft Office including Word, Excel, Visio and PowerPoint</li><li>Outstanding verbal and written communication skills</li><li>Strong data management abilities</li></ul><div> </div><div> </div><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div><strong> </strong></div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.</strong></div>
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Aug 13th, 2020 04:23PM
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Aug 13th, 2020 04:23PM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Oct 22nd, 2020 12:00AM
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Senior Director, Software Engineering - Digital Health
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Open
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Engineering
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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Oct 21st, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and well being of people around the globe with respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology. </div><div> </div><div>Digital technology is playing a larger role within healthcare today. Quidel is currently known as a leader in connected Point-of-Care diagnostics. We strongly believe that customers want technology to improve their testing experience and outcomes. We introduced the Virena platform for disease surveillance in 2014. With thousands of instruments contributing real time information, we can assist healthcare professionals understand key public health trends in their local communities. However, that is just the beginning. Working within the Digital Health team, you can help take us to the next level using technology to enhance and expand diagnostics. Join the future of medical technology with a proven industry leader.</div><div> </div><div>Quidel is looking for a Senior Director, Software Engineering - Digital Heath to join our team in the Mira Mesa area of San Diego. The Senior Director, Software Engineering – Digital Health will be part of a highly collaborative and multidisciplinary team that develops and supports a diverse set of digital properties that enhance the in-vitro diagnostic testing process for Quidel customers. You will be the lead for all software development and support in this function. </div><div> </div><div><strong>Essential Functions:</strong></div><div>Develop a team of software engineers that focus on software applications responsible for products assisting and enhancing diagnostic testing in traditional and new markets.</div><ul><li>Align teams around the strategic vision of how software can be used to take diagnostic testing to the next level.</li><li>Work with customers, Quidel colleagues, and external collaborations to design user-centric solutions that provide scalability, reliability, highly sustainable performance, and compliance. </li><li>Define and manage software development priorities – you will have multiple product roadmaps which will need to be harmonized. Define and articulate timelines, costs, and execution schedules.</li><li>Drive a standard of cybersecurity protocols required for App and Cloud environments required for FDA compliance and user acceptance.</li><li>Use your keen understanding of software application design and development principles and regulatory requirements to establish a standard for agile software development among the team.</li><li>Carries out duties in compliance with established business policies</li></ul><br/><br/><div><div><strong><span style="text-decoration: underline;">Education/Experience:</span></strong></div><ul><li>Bachelor’s degree required, in Computer Science, Engineering, or a Business-related field; Masters degree preferred</li><li>A minimum of 15+ years professional experience designing and developing software solutions that solve large scale and complex business problems, 10 years in a leadership role of technical personnel is expected.</li><li>A minimum of 5 years in medical device software or digital health applications</li><li>Demonstrated track record in building creative, high-performing teams</li><li>Must demonstrate prior experience delivering cloud based applications that scale. We have thousands of instruments across the world performing millions of diagnostic tests – so all software applications need to be designed for performance and reliability at scale.</li><li>Deep understanding of modern technology, architectures, and agile development methods across cloud and mobile platforms. </li><li>Prior professional experience in a FDA regulated environment – knowledge of regulatory standards IEC 62304, ISO 13485, MDDS, HIPAA</li></ul><div><strong><span style="text-decoration: underline;">Knowledge/Skills:</span></strong></div><ul><li>Passionate about analyzing problems and solving technical challenges to improve testing outcomes in the healthcare system</li><li>Highly collaborative – able to work with colleagues across multiple functions at all levels of the organization. Builds strong and trusting relationships.</li><li>Prior experience working with contracted software partners is desired</li><li>Demonstrated ability to work across geographic boundaries</li><li>Deep knowledge of the MS Azure environment.</li><li>Strong ability to understand data relationships and data modeling</li><li>Basic knowledge of Microsoft Office products</li></ul></div><div> </div><div>Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div> </div><div><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.</strong></div>
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Oct 22nd, 2020 07:24AM
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Oct 22nd, 2020 07:24AM
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Quidel
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Health Care
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Health Care Equipment & Services
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nasdaq:qdel
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www.quidel.com
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search10.smartsearchonline.com
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Oct 23rd, 2020 12:00AM
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Software Configuration Engineer
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Open
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R & D
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San Diego, CA, 92121, US
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San Diego
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CA
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USA
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May 27th, 2020 12:00AM
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<div>Quidel Corporation is a leading manufacturer of diagnostic healthcare solutions serving to enhance the health and wellbeing of people around the globe with well-known and respected products that provide healthcare professionals with accurate and cost-effective diagnostic information at the point of care (POC). Our core competencies and capabilities focus on immunoassay and molecular testing in the areas of: infectious disease, cardiology, women’s health, and virology.</div><div> </div><div>The Software Configuration Engineer will be working in a highly collaborative R&D environment with multidisciplinary teams to support an array of diverse software development projects related to the development and commercialization of diagnostic instrument platforms.</div><div> </div><div><strong>ESSENTIAL FUNCTIONS:</strong></div><div><strong> </strong></div><ul><li>Identifies issues to be addressed and areas of concern where IVDR may hinder the registration and sale of Quidel products</li><li>Interact with R&D, Information Systems (IS) and external contractors to create/structure repositories and continuous integration build systems</li><li>Maintain source code repositories, build systems, issue tracking and project management tools</li><li>Provide input to development and V&V teams to structure projects and test frameworks which are efficient, fault tolerant and extensible</li><li>Collaborate with Instrument Systems teams regarding data, document retention</li><li>Revise and maintain build and test systems to ensure best practices</li><li>Develop, structure and maintain source code repositories in Git and Azure</li><li>Experience with Azure Dev Ops related tools and systems for issue tracking and project tracking</li><li>Design and implement reliable and effective continuous integration build systems</li><li>Debug and solve build issues and automated test framework issues.</li><li>Maintain defect tracking and agile management tools</li><li>Develop strategies for V&V test framework implementation to build systems</li><li>Create and publish release notes appropriate for the intended uses of interim and commercial software releases</li><li>Develop, structure and maintain software configuration files for diagnostic instruments and prototypes used in development</li><li>Carries out duties in compliance with established business policies</li></ul><br/><br/><div ><strong>Education/Experience</strong></div><ul><li>Preferably a Bachelor’s Degree in Computer Science or Electrical Engineering and a minimum of 5 years of experience.</li><li>Experience in a medical device environment required.</li></ul><div ><strong>Knowledge/Skills</strong></div><ul><li>Experience with continuous integration software compilation, integrated unit test execution and release processes</li><li>Programming skills in one of the following. Python, Java or C++</li><li>Experience with Git repository, establishing, managing and maintaining repositories.</li><li>Experience with automated testing with unit testing and automated testing on target platforms.</li><li>Experience with Linux and Windows</li><li>Experience with software tools such as JIRA or Azure tools</li><li>Excellent prioritization and organizational skills are needed to be successful in this role. The ability to multi-task is required. </li><li>Excellent communication skills (verbal and written)</li><li>Experience in QSR (Quality System Regulations) and a knowledge of Design Control</li><li>Prior experience in working with OEM or contracted software partners is desired</li><li>Demonstrated ability to work in cross-functional and geographically dispersed teams. </li></ul><div >Before you apply, please make sure you share Quidel’s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be <strong>customer driven</strong>, <strong>focused on execution</strong>, and <strong>new product oriented</strong>. We succeed by being <strong>determined</strong>, <strong>optimistic team players</strong>.</div><div ><strong> </strong></div><div ><strong>Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.</strong></div>
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Oct 23rd, 2020 06:12AM
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Oct 23rd, 2020 06:12AM
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Quidel
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Health Care
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Health Care Equipment & Services
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