Contract Quality Engineer Jobs

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CSV Consultant
PrincetonNegotiable

Please note: Applicants must hold an EU passport or existing right to work in the EU (no sponsorship available). Fluency in French or Dutch is mandatory.A leading pharmaceutical/biotech organisation is seeking an experienced Computer System Validation (CSV) Consultant to support critical projects in compliance with GAMP 5 guidelines. This role offe...

Quality Engineer
AmsterdamNegotiable

The Quality Engineer collaborates closely with the engineering team to identify and understand critical-to-quality design attributes and specifications. This role involves reviewing and releasing custom hardware, sub-project, and project DHF documentation to ensure compliance with all applicable regulatory requirements. The individual will contribu...

Senior CSV Specialist
ToulouseNegotiable

We are seeking a Senior CSV Consultant to lead validation activities across a broad scope of systems. This role sits within the technical operations function, which covers new product introduction, CQV, CSV, automation, and supporting services. The consultant will act as the internal lead for computer system validation, coordinating external consul...

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Senior CSV consultant
ToulouseNegotiable

Un nouveau site de fabrication de biomédicaments à Toulouse entre dans sa phase de lancement, avec des installations et des systèmes digitaux déjà en place pour soutenir la production d'anticorps monoclonaux. Le site est doté de laboratoires, d'utilités et de plateformes numériques de pointe, et recherche un Consultant Senior CSV (H/F) pour pilote...

Process Development Consultant
Braine-l'AlleudNegotiable

Eligibility Requirement: Candidates must hold valid rights to work in the EU/Belgium. Assignment PurposeSupport the transfer and scale‑up of new processes between R&D and manufacturing. Provide technical expertise, project leadership, and cross‑functional coordination to ensure smooth integration of innovations into production. Scope of WorkAct as ...

CQV Engineer
ParisNegotiable

This is a contract position with a leading pharmaceutical/biotech organization, requiring candidates to hold full rights to work in France/EU. Successful applicants will support commissioning, qualification, and validation (CQV) activities across multiple French sites. The role offers strong potential for extension and progression into more senior ...