MSAT Visual Inspection Expert
About the Job
We deliver 4.3billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as Visual Inspection Expert within Manufacturing Science Analytics & Technology (MSAT), will be to drive and support visual inspection by delivering automated systems and driving standardization, harmonization of practices, innovation, and scientific excellence across the Injectables platform. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives.
Main Responsibilities
- Serve as an MSAT point of contact for Automated Visual Inspection recipe creation, tuning and troubleshooting for visual inspection of filled containers (e.g., vials, pre‑filled syringes).
- Collaborate closely with stakeholders to drive reduction in reject rates in inspection systems whilst ensuring compliance to global standards.
- Provide troubleshooting support to commercial visual inspection operations.
- Work independently and across teams to identify inspection issues, formulate solutions and implement changes as required.
- Ensure compliance with all regulatory requirements and good documentation to provide a safe, quality, and effective product.
- Act as a connector with the main partnering functions (MSAT Injectables Techno Platforms, Injectable Manufacturing Network sites, Quality and MSAT Digital, External Supply and Centre of Excellence Groups) to deliver those key objectives and make them successful within MSAT.
- Train and mentor new and current associates on the visual inspection program including recipe creation, tuning, troubleshooting and recipe management.
- Continuously seek innovative, cost‑effective solutions, harmonization and standardization approaches for inspection and all Injectable processes throughout the product lifecycle.
- Drive and champion benchmarking activities within the Sanofi network and the wider pharmaceutical industry to define and disseminate industrial best practices.
- Support network sites for development projects and/or complex manufacturing investigations.
What We Offer
A fixed salary over 12 months, supplemented by individual variable compensation, as well as profit‑sharing and incentive bonuses based on Sanofi Group results. Because taking care of our employees is also our mission: 31 days of paid leave + RTT days (reduced working time days) according to your status, remote work up to 2days/week, quality health insurance, public transportation coverage up to 80%; maternity leave (18weeks) and parental leave for welcoming a child (14weeks), Savings Plan & Retirement Plans with employer contributions, Works Council benefits, internal and international mobility opportunities, a customizable training program to support you throughout your career, and many other benefits.
About You
- Education: Degree in electrical, mechanical and/or other applicable engineering field required. Advanced Science degree is preferred.
- Experience: 5+ years’ experience working with visual inspection equipment in a pharmaceutical cGMP environment or equivalent.
- Technical and soft skills: Understanding of current pharmacopeia guidance and regulations regarding visual inspection; deep understanding of GMP and CMC requirements by health authorities and experience in preparation and reviews of regulatory dossiers and interactions; ability to inspire teams; effective communication and people skills; experience and ability to operate in multidisciplinary and multi‑cultural teams; experience in participating in transformation programs to accelerate development, technology transfer, validation, and manufacturing support.
- Language: Fluency in English is required for this role.
Salary
Salary range: €48000,00 – €64000. Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in company employee benefit programs.
Equal Employment Opportunity Statement
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Assertive Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; appearance or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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