gmp operation apprentice Jobs in Luzern

MSD is seeking a Specialist Upstream Operations in Switzerland to support GMP manufacturing of early-phase biologics. The role requires full-time site presence at Schachen, Zurich area, and involves setting up upstream operations, ensuring GMP compliance, and documentation throughout process transfers and CAPA investigations.You will mentor junior staff,...

LHH is seeking a Process Engineer (Associate Specialist Downstream Operations) in the Lucerne area for a 12-month, onsite assignment at a leading biotech facility. The role focuses on purification, GMP manufacturing, and collaboration with cross-functional teams to deliver clinical-stage therapies.Ideal candidates hold a relevant science degree with 1–2...

LHH is assisting a leading global biotechnology client in the Lucerne area to hire a Production Operator II (m/f/d) for a state-of-the-art biologics manufacturing facility in Schachen.In this hands-on role, you will support Weigh & Dispense, Solution Supply, USP and DSP operations in GMP cleanrooms, perform sampling, equipment setup, documentation, and...

Michael Page is recruiting for a prestigious pharmaceutical company on a temporary 12-month contract in Luzern. The role supports cross-functional teams on equipment operation, including preparation, setup, sampling, and material management on the shop floor.You will monitor GMP status, calibrate and maintain equipment, review batch documentation, and...

Randstad Switzerland is seeking a Production Operator for an international pharmaceutical company in Lucerne. You will join the Biologics Manufacturing Science and Operations team and support Drug Substance Bioprocess on a 1-year term, onsite only.The role requires 1 year in pharma/biotech, familiarity with GMP processes, and strong German and English...

CK QLS is seeking a Junior Production Operator to join a global Biopharmaceutical company in Lucerne on a 12-month contract. You will be part of the Biologics Manufacturing Science and Operations department, Drug Substance Bioprocess.Key duties include equipment handling on the shop floor, GMP-compliant documentation, batch review, and coordinating daily...

Merck & Co., Inc. in Lucerne (Schachen/Werthenstein) seeks a Specialist Upstream Operations to support GMP manufacturing of early-stage biologics and to integrate with an existing team.You will set up and execute upstream processes, manage deviations and CAPAs, and drive continuous improvement while collaborating with QA, IT systems, and manufacturing...

## Specialist Upstream Operations (m/f/d)Apply: Not Applicable: CHE - Lucerne - Schachen (Werthenstein): Full time: Posted Today: End Date: September 29, 2026 (13 days left to apply): R414073Job DescriptionOur Schachen serves as a magnetic force that attracts, recognizes, and integrates people from diverse backgrounds and perspectives. Employees...

LHH is seeking a detail-oriented Documentation Specialist (m/w/d) to join our Manufacturing Operations team at the Schachen site in Switzerland. You will work closely with Metrology & Validation and Compliance to maintain GMP documentation and ensure ongoing inspection readiness.Responsibilities include managing document storage, developing a digital...

CK QLS is seeking an Associate Specialist in Downstream Operations for a 12-month, full-time on-site role in the greater Lucerne area. The position focuses on supporting GMP manufacturing of early-stage therapies, with responsibilities spanning setup, execution, and documentation of downstream processes.The candidate should have 1–2 years of pharma/biotech...

LHH Recruitment Solutions in Switzerland seeks a Documentation Specialist (m/w/d) to join our Manufacturing Operations team in a GMP biopharmaceutical environment at Schachen.You will support Metrology & Validation and Compliance teams with digital documentation management, archiving, and ensuring accessibility of records. The role offers development...

Michael Page in Switzerland is seeking a Documentation & Compliance Coordinator to support GMP-regulated operations. You will manage the documentation lifecycle, coordinate control activities across lab equipment, validation, and training records, and help implement digital document management solutions.The role requires a life sciences or QA background,...

Alcosuisse AG Betrieb Schachen seeks a Specialist Upstream Operations to support GMP manufacturing of biologics in a full-time role. The site in Schachen LU supports early-phase clinical supply and integrates advanced technologies into the manufacturing pipeline.Expect to work on-site with a diverse team, ensuring quality, continuous improvement, and...

We are currently seeking a detail-oriented Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment. The candidate will work at the local site and in alignment with our global Metrology & Validation and Compliance teams. The position offers development potential, and...

Client Description For one of our clients, a leading global biotechnology company located in the greater Lucerne area, we are currently seeking a Process Engineer (Associate Specialist Downstream Operations) (m/f/d) to join a state-of-the-art biologics manufacturing facility in Lucerne area. This innovative manufacturing site specializes in the development...

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...

Client Description For one of our clients, a leading global biotechnology company located in the greater Lucerne area, we are currently seeking a Senior Specialist, Strategy & Operational Excellence (m/f/d) to join a state-of-the-art biologics manufacturing facility supporting early clinical development programs. For one of our clients, a leading global...

MSD Malaysia is seeking a Specialist Upstream Operations in Schachen, Switzerland, to support GMP manufacturing and to integrate into an existing team. You will help set up and troubleshoot upstream operations in fed-batch processes while ensuring GMP and EHS compliance and timely documentation of deviations and CAPAs.You should have 2–5 years in...

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...

Prestigious pharmaceutical company Temporary 12 month contract // Start 1.October // Onsite role About Our Client Prestigious pharmaceutical company Job Description Operational Excellence & Continuous Improvement Lead and drive Operational Excellence initiatives across the site to improve efficiency, reduce complexity, and enhance overall business...