Biomrieux

We are seeking a highly skilled Automation and Verification Engineer to join our dynamic team, driving robustness of hardware, software, firmware, and algorithms into systems that shape the future of medical science.. QC scientist works in a cGMP environment performing quality control testing for commercial diagnostics products.. Practices good lab safety according to OSHA/EHS regulations and Good Laboratory Practice (GLP), as well as other applicable regulations.. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux’s bonus program.. A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options

qc scientist

Want to see more? Find all job opportunities for both BioFire and bioMérieux worldwide by clicking here. Description bioMérieux is a pioneering force in the medical microbiology device industry. Our cutting-edge technologies have been transforming healthcare and improving patient outcomes. We are seeking a highly skilled Automation and Verification Engineer to join our dynamic team, driving robustness of hardware, software, firmware, and algorithms into systems that shape the future of medical science. Position Details QC scientist works in a cGMP environment performing quality control testing for commercial diagnostics products. Responsibilities include inspection and testing of products to approved specifications according to approved processes and procedures. Works closely with the manufacturing team to maintain production schedule, elevate quality issues, and ensure quality of production batches. Performs all duties using quality mindset and safety conscious practices. Primary Duties <ul><li>Conducts routine QC testing of incoming raw material, finished goods, and stability products. </li><li>Manage QC testing schedule alongside production schedule to ensure timely closure of work orders. </li><li>Document results, issues, and other relevant information using good documentation practices (GDP) under the site Quality Management System. </li><li>Reviews production batch records and QC test results for accuracy, completeness, and GDP. </li><li>Supports and executes protocols for analytical test methods and aids in the transfer of methods to QC. </li><li>Analyzes, prepares, and communicates data findings, trends, non-conformances, and deviations. </li><li>Assists as needed with investigations to determine root cause of non-conformances. </li><li>Maintain lab equipment compliance by ensuring preventative maintenance and calibrations are completed on time. </li><li>Supports environmental monitoring of production spaces. </li><li>Performs subculture of organisms required for testing, ensuring organism availability. </li><li>Run instrumentation including, but not limited to UV-Vis and FTIR spectrophotometers, and microbiological diagnostic equipment. </li><li>Maintains inventory and orders lab supplies as needed. </li><li>Practices good lab safety according to OSHA/EHS regulations and Good Laboratory Practice (GLP), as well as other applicable regulations. </li><li>Updates QC procedures and/or specifications as needed. </li><li>Ensures cleanliness of QC laboratory</li><li>Trains new team members as needed. </li></ul>Knowledge, Experience, And Skills <ul><li>BS in biology, chemistry or related scientific field and a minimum of 3 years’ relevant laboratory experience. </li><li>Good hygiene and aseptic practices, with experience working with hazardous chemicals and microorganisms. </li><li>Medical Device or other FDA regulated industry experience required. Must possess working knowledge of good laboratory practices, GMP, and antibiotic/microorganism interactions. </li><li>Must possess effective written and verbal communication skills. Must possess ability to read and interpret common scientific methods, procedures, and regulatory guidelines. </li><li>Requires strong computer skills including Microsoft Office Package (Excel, Word, etc.). </li><li>Self-motivated, highly organized, with ability to multitask and open to learning new skills. Must be able to work in a team environment, building effective working relationships. </li></ul>The estimated salary range for this role based in California is between $87,200 and $104,600 annually. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux’s bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate’s experience and will be presented in writing at the time of the offer. In addition, bioMérieux offers a competitive Total Rewards package that may include: <ul><li>A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options</li><li>Company-Provided Life and Accidental Death Insurance</li><li>Short and Long-Term Disability Insurance</li><li>Retirement Plan including a generous non-discretionary employer contribution and employer match. </li><li>Adoption Assistance</li><li>Wellness Programs</li><li>Employee Assistance Program</li><li>Commuter Benefits</li><li>Various voluntary benefit offerings</li><li>Discount programs</li><li>Parental leaves </li></ul>BioFire Diagnostics, LLC. is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioFire Diagnostics’ application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

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