Quality Specialist Jobs
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Batch Records Writer
Production Batch Records Writer (Contract) Contract Length: 2 months Hours: Full‑time (40 hours per week) Work Setup: Remote About the RoleA confidential organisation in the chemical/pharmaceutical sector is seeking an entry‑level Production Batch Records Writer to support the consolidation, authoring, and completion of drug‑substance batch records...
QA Investigator II
Quality Assurance InvestigatorLocation: Lenoir, NCEmployment Type: Full-Time, On-SiteSalary Range: $65,000-$80,000/year Position SummaryA growing pharmaceutical manufacturing organization is seeking a Quality Assurance Investigator to support its quality systems and compliance efforts. This role is responsible for investigating quality events, supp...
QA Investigator II
Quality Assurance InvestigatorLocation: Lenoir, NCEmployment Type: Full-Time, On-SiteSalary Range: $65,000-$80,000/year Position SummaryA growing pharmaceutical manufacturing organization is seeking a Quality Assurance Investigator to support its quality systems and compliance efforts. This role is responsible for investigating quality events, supp...
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Scientist
Standort: Visp, Schweiz Vertragsdauer: 01. Februar 2026 - 31. Januar 2027 Homeoffice: Möglich (hybrides Modell)Wir unterstützen ein führendes Unternehmen im pharmazeutischen Sektor bei der Suche nach einer/m Wissenschaftler/in für das Team in Visp, Schweiz. Diese Position bietet die Möglichkeit, an hochrelevanten Projekten in einem cGMP-konformen U...
QA Operations Associate Manager
Our client is a global life science company specialising in cutting edge solutions for biologics, cell and gene therapies driving excellence in manufacturing and quality.They are currently looking for a QA Operations Associate Manager to manage the day to day QA operations in the manufacturing facility.Responsibilities:Oversee daily Quality Assuran...
Sterilisation Validation
The Consultant will lead and support sterilisation strategy, validation, and compliance activities across the full lifecycle of medical devices, including Class IIa. The role requires deep expertise in sterilisation modalities, microbiological testing, and regulatory frameworks under both FDA and EU MDR. Job Title: Sterilisation ValidationDuration:...