Automated Visual Inspection Specialist
Join a major pharmaceutical company's injectable manufacturing sites to work on automated visual inspection systems for vials, syringes, and other parenteral products. This role involves recipe development, vision algorithms, equipment qualification (IQ/OQ/PQ), troubleshooting, and continuous improvement, all while maintaining strict cGMP and regulatory compliance.
Key Responsibilities
- Develop recipes and vision algorithms for automated visual inspection systems.
- Execute equipment qualification processes including IQ, OQ, and PQ.
- Perform troubleshooting and drive continuous improvement initiatives.
- Maintain strict adherence to cGMP and regulatory compliance standards.
Qualifications
- Bachelor's degree in Engineering (Mechanical, Electrical, Automation, Optical, Biomedical, or similar).
- 7+ years of hands-on experience in pharmaceutical or biopharma manufacturing, ideally with injectable products.
- Strong experience with AVI platforms and vision software.
- Solid understanding of cGMP, Annex 1, USP guidelines, and data integrity.
- Confident English communication skills; local language proficiency is a bonus.
- Right to work in the EU.
Role Details
- Location: Italy, France, or Germany (On-site).
- Contract Duration: 6 months.
- Start Date: December 2026.
If you enjoy the technical side of AVI and want to influence equipment decisions as well as execute them, this is a great opportunity.