Quality Auditor Oss • SIRE Life Sciences
Gevraagd
-
37 - 40 uur
Aanbod
-
Vast contract
Vacature in het kort
Over het bedrijf
Volledige vacaturetekst
The company
As a global leader key biotechnology and pharmaceutical site within global network. The facility focuses on the production, packaging, and quality assurance of innovative medicines and vaccines, supporting global health with high standards in compliance, safety, and collaboration
Role Description
As a Quality Auditor, you support batch-related quality activities at Oss Biotech, ensuring compliance with GMP standards and internal procedures. You act as a quality advisor, contribute to continuous improvement, and help maintain oversight of manufacturing and packaging processes.
Responsibilities
- Review batch records and related GMP documentation (e.g., logbooks, cleaning records).
- Perform Usage Decisions for materials produced by IPT.
- Support and approve investigations, CAPAs, and change controls.
- Prepare release documentation and ensure timely batch release.
- Provide quality guidance to cross-functional teams.
- Track and report quality metrics regularly
- Promote safe, compliant, and efficient operations in line with EHS policies.
- Bachelor’s degree (HLO) in Biotechnology, Chemistry, or a related field.
- At least 2 years of experience in pharmaceutical quality operations.
- Solid knowledge of GMP/GDP and quality systems (deviations, CAPA, change control).
- Fluent in Dutch and English; SAP experience is a plus.
Interested
Are you interested in this or a similar role?
55135
Gerelateerde zoekopdrachten
Auditor OssFulltime OssVast contract OssOssProvincie Noord-BrabantAuditorSalaris AuditorVanaf nu ontvang je automatisch de best passende vacatures automatisch in je mailbox.
Jouw inschrijving
Emailadres:
Functie:
Plaats:
Frequentie:
Wijzig je inschrijving
