Contract Quality Engineer Jobs

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Quality MDR Specialist
MontmorencyNegotiable

Role DetailsContract: 12 monthsLocation: Ile-de-France, France - Hybrid (around 80% onsite presence required)Start date: ASAPLanguages: French (required) & Professional English Key ResponsibilitiesSupport the ongoing MDR transition within the Quality teamLead or contribute to risk assessments aligned with MDR requirementsProvide expert guidance on ...

IT Compliance manager (CSV Manager)
LilleNegotiable

The IT Compliance Manager (CSV Manager) will be responsible for ensuring that computerized systems used in a pharmaceutical manufacturing environment are validated, compliant with regulatory requirements, and maintained in a validated state throughout their lifecycle. The successful candidate must have prior experience working within pharma manufac...

QC Project Engineer
SalamancaNegotiable

Location: Salamanca, Spain (Onsite)Contract: 12-month contract, full-timeThe Quality Control Project Engineer will join a multidisciplinary team supporting the expansion of a Quality Control laboratory. The role is responsible for the technical delivery of multiple critical systems from construction through commissioning, ensuring compliance with q...

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CQV Engineer
NeuchatelNegotiable

Dans le cadre d'un projet d'envergure au sein d'une société pharmaceutique située dans la région de Neuchâtel, nous recherchons un Ingénieur CQV expérimenté pour accompagner les activités de qualification d'équipements de production, incluant les étapes FAT, SAT, IQ, OQ, PQ ainsi que des systèmes HVAC.Responsabilités principalesPréparer, exécuter e...

CQV Engineer
NeuchatelNegotiable

Dans le cadre d'un projet d'envergure au sein d'une société pharmaceutique située dans la région de Neuchâtel, nous recherchons un Ingénieur CQV expérimenté pour accompagner les activités de qualification d'équipements de production, incluant les étapes FAT, SAT, IQ, OQ, PQ ainsi que des systèmes HVAC.Responsabilités principalesPréparer, exécuter e...

Senior CQV Specialists
AltkirchNegotiable

A major global pharmaceutical company is building a new state‑of‑the‑art facility in France, covering aseptic manufacturing and high‑performance clean utilities. To support the commissioning, qualification, and validation (CQV) program, the client is seeking experienced CQV Consultants with strong technical depth and the ability to operate in a Fre...