A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux provides diagnostic solutions that detect disease and contamination to improve patient health and ensure consumer safety. In North America we have more than 5,000 team members across 12 sites or subsidiaries, including Salt Lake City based BioFire Diagnostics. We believe in the power of diagnostics and bioMérieux sponsors public health initiatives and partnerships to address antimicrobial resistance, sepsis awareness, food safety, and consumer health across the globe. Come be a part of our mission to help save lives. Position Summary:
Develop, support and implement basic validation initiatives as defined in site goals and objectives. Responsible for the coordination and documentation of validation efforts with other departments providing validation guidance to all levels for quality assurance, compliance, and continuous quality improvement. Ensure products are developed, manufactured, tested, and delivered according to established procedures that will assure they meet all validation requirements. Develop and execute equipment, material, cleaning, and process validation protocols including statistical analysis of data generated by validation studies Main Accountabilities: Coordinate and document validation efforts with other work groups including Engineering, QC, and R&D, acting as the primary validation interface between Engineering and QA. Develop and execute equipment, material, cleaning, and process validation protocols including statistical analysis of data generated by validation studies and compiling relevant documentation. Assure validation documentation is generated, reviewed and approved in accordance to procedures. Contribute as validation subject matter expert by sharing technical expertise across departments, mentoring individuals to ensure knowledge consistency, and providing primary validation support to audits. Identify, evaluate, and manage risk by utilizing techniques such as FMEA, Fault Tree Analysis, Fishbone Diagram, HACCP, etc. Integrate risk based decision making with the validation life-cycle. Support Change Control Processes through assessment of system changes, and execution of revalidation and/or re-qualification activities as needed. Ensure validated state is maintained by performing periodic review of equipment, processes, etc. Review and approve engineering specification documents. Studies, Experience, Skills and Qualifications:
- Requires Bachelors Degree in Engineering or Life Science and a minimum of seven (7) years experience performing primary duties in health care or a related regulated industry; or a Masters Degree and five (5) years experience performing primary duties in health care or a related industry.
- Excellent personal hygiene required in production and laboratory areas.
Joining bioMérieux, is choosing to join an innovative company with a long term vision, committed to the service of public health and carried out with a humanistic corporate culture. Our Group offers numerous possibilities: so come and join the 13,000 bioMérieux team members who already identify with these values!
bioMérieux is an Equal Opportunity, Affirmative Action Employer. M/F/Vet/Disability/Sexual Orientation/Gender Identity/GINA.
Job ID: 16145