Quality Engineer I

1. Monitor a product portfolio intended to food and/or pharmaceutical industrial diagnostic (reagents, instruments, software; microbiology, molecular biology, immunology); as such, you will be: Member of the project teams for developing or modifying these products. The preferred contact and the guarantor of the quality processes implemented throughout the product lifecycle (such as design control, design change management, field actions management), in accordance with bioMerieux, international and customer requirements.
2. Pilot and ensure that product risk management is controlled all along the product lifecycle.
3. Be able to challenge and to propose alternatives on technical and strategic choices and decisions made in the projects, with regards to risk-taking on quality and business aspects; be able to escalate wisely.
4. Manage the organization of Field Action Board meetings in charge of deciding on the actions to be taken in the field in the event of problems with the marketed products; as such, you will interface with GiCS (global industry customer service) representatives, manufacturing site quality manager, program directors and Industrial Applications Quality Managers.
5. Be the preferred contact for other functions, on quality processes for your product ranges.
6. Support the teams for audit preparation and be the preferred audit contact for quality purposes about development and field actions on your product portfolio.
7. Contribute to improving the product lifecycle efficiency or any quality process required within the Industry Unit; as such, you will coordinate or contribute to continuous improvement initiatives as well for your ranges as for overall practices harmonization, interfacing with other professions.
8. Perform all work in compliance with company quality procedures and standards.

• Bachelors degree in a Scientific field required.
• Master's degree preferred.
• 2 years' experience in Quality or Research and Development
• Including expereince in PCR, molecular biology, microbiology techniques and diagnostic product development.
• Industry experience preferred.
• Quality job and design control for the development of reagents and/or instruments experience is preferred.

• Knowledge of standards applicable to design control and to pharma and/or food field (ISO 9001, ISO 13485, ISO 14971, 21CFR820, GAMP, 21CFR11, GMPs, ISO 16140 ...) and the capacity to act as a quality auditor.
• Knowledge in the interpretation and application of relevant Domestic and International Regulations and Industry Standards (e.g. ISO, QSR, IVDR, AFNOR etc.).
• Knowledge of the industrial domain is strongly expected (pharmaceutical, cosmetic, food industries) Experience in participation in the management of regulatory audits (i.e. ISO 9001,ISO 13485, FDA, etc.).
• Manage and meet competing deadlines, requiring careful prioritization and time management to ensure all tasks are completed on time.
• Understand complex information and interpret it accurately, often requiring critical thinking and analysis to grasp the full picture.
• Effectively deal with ambiguity requiring adaptability, critical thinking, and proactive communication to navigate situations with limited details
• Informing others by sharing clear, timely information to ensure alignment.
• Functional skills including critical thinking, adaptability, time management, communication, problem-solving and digital literacy.
• Critical thinking, using logic and reason to analyze information and make decisions in the workplace
• Managing and measuring work by tracking progress, performance, and goal achievement using metrics and KPIs.
• Communicates instructions clearly and effectively
• Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives
• Ability to cooperate with others at all levels including leadership
• Consistently uphold and reflects the core ethical principles and values that bioMerieux promotes

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BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. 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 BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).