gmp documents Jobs in Luzern

nemensis ag seeks a Manufacturing Operator (m/f/d) to join the Drug Substance Bioprocess team in Schachen, LU. You will work in a GMP-regulated biopharma setting, ensuring safe, precise, and timely production of biologics. The assignment runs 01.10.2026–30.09.2027 as a temporary placement, with 100% workload.You will set up equipment, prepare materials,...

Duration: 6 monthsHome office and hybrid working:This is a site-based role, 5 days per weekOpportunity for home office is available on a need basis and in coordination with manager.Position OverviewYou will join the Pharmaceutical Analysis & Digital Technologies (PADT) department and help develop and maintain a robust documentation management process that is...

The QA Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing Operations and focuses on right‑first‑time execution, documentation...

Michael Page is representing a leading Swiss pharmaceutical/life sciences organization based in Luzern. The role focuses on managing and maintaining documentation across its lifecycle in a GMP-regulated setting, collaborating with Quality, Validation, Compliance, and technical teams to ensure inspection readiness.You will support audits, implement digital...

About Our ClientOur client is a leading international organization operating within the pharmaceutical and life sciences sector. Based in Switzerland, the company is committed to quality, compliance, and continuous improvement across its laboratory and operational functions. This position offers the opportunity to work closely with technical, validation, and...

Manufacturing Asset SpecialistJob ID: REQ-058080Location: Schachen, Entlebuch District, Canton of LucerneJob Type: RegularPerkinElmer's OneSource team is looking for a Manufacturing Asset Specialist to support the Team on Customer site (MSD) in Schachen.More information about PerkinElmer and our business : PerkinElmer | Science with Purpose (opens in new...

PerkinElmer's OneSource team is seeking a Manufacturing Asset Specialist to support the MSD Customer site in Schachen, Switzerland. The role focuses on document review, asset release, and data management within calibration and maintenance processes.You will collaborate with calibration and maintenance engineers, handle regulatory documentation, and ensure...

Specialist, Planning & Scheduling (m/f/d) The Specialist, Packaging Compliance Support, is responsible for supporting packaging compliance activities across batch record preparation and review, investigations, documentation, training support, and operational coordination. This role helps ensure that packaging support processes are executed in alignment with...

PerkinElmer's OneSource team is looking for a Manufacturing Asset Specialist to support the Team on Customer site (MSD) in Schachen. MoreinformationaboutPerkinElmer and our business : PerkinElmer | Science with Purpose More information about our OneSource services: OneSource Laboratory Solutions | PerkinElmer Hybrid working model Responsibilities: Document...

Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that's devoted to delivering a high-quality, reliable supply to customers and patients on time, every time.Our site in...

Job Description Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that’s devoted to delivering a high‑quality, reliable supply to customers and patients on time,...