batch Jobs in Luzern

GMP Batch Documentation Specialist (m/f/d) Make Every Batch Record Count as GMP Batch Documentation Specialist (m/f/d) - Assignment period: 26 October 2026 – 30 June 2027 - Location: Schachen (LU) - Employment type: Temporary placement via nemensis ag Our client Our client is an internationally active biopharma company specializing in clinical...

Destinus is seeking a Propellant Production Technician at our Lucerne facility. This hands-on, safety-critical role focuses on solid rocket motor propellant production in a regulated environment, with emphasis on accurate documentation and strict quality control.You will mix, cast, cure and inspect batches, operate casting stations and ovens, maintain batch...

CK Group seeks a Quality Auditor to join its CK QLS division in Schachen, working within the Global Development Quality Operations team. The role focuses on GMP documentation review, supporting batch release decisions, and maintaining high standards of GMP compliance. The candidate should have QA/Quality Operations experience in a regulated environment,...

For one of our clients, an international pharmaceutical company, we are seeking a Quality Assurance Operations Specialist.General Information:End Date: 31.10.2028Home office: Possible, 2 days per weekWorking hours: StandardAbout the work:The Global Development Quality OPS team is responsible to drive or support compliance-based programs and results which...

About the Role The Destinus engineering team is seeking a Propellant Production Technician to support the serial manufacturing of solid rocket motor propellant at our Lucerne facility. The role is hands‑on and process‑focused, working directly with energetic and chemical materials in a tightly regulated, safety‑critical production environment. The...

Specialist GDQ QOS (M/F/D) The Global Development Quality OPS team is responsible to drive or support compliance-based programs and results which include support cross functional projects, solving simple problems, current Good Manufacturing Practices (cGMP) quality initiatives, quality system improvements, quality directives, compliance metrics and...

Quality Auditor CK QLS is recruiting a Quality Assurance Specialist to join the Global Development Quality Operations team at a leading pharmaceutical company in Schachen. This opportunity is suited to a quality-focused professional who enjoys reviewing GMP documentation and supporting compliance within a pharmaceutical environment. Your responsibilities *...

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...

Associate Specialist Downstream Operations (12 months) Duration: 1 year This is an Associate Specialist position within the Downstream Operations group at our company in the greater Lucerne area. This role requires full-time on-site presence to support manufacturing and integrate seamlessly with the existing team. As a member of the manufacturing team at our...

Client DescriptionFor one of our clients, a leading global biotechnology company located in the greater Lucerne area, we are currently seeking a Production Operator II (m/f/d) to join a state-of-the-art biologics manufacturing facility in Schachen. This innovative manufacturing site specialises in the development and production of biologic drug substances...

On behalf of our client, a global leader in the pharmaceutical industry, we are seeking a GMP Documentation Specialist to support clinical biologics manufacturing operations for an 8-month project in the Lucerne Region. In this role, you will play a key part in ensuring GMP-compliant documentation, batch record accuracy, and data integrity across...

Werthenstein BioPharma GmbH in Switzerland is seeking a Specialist, Planning & Scheduling (m/f/d) to support packaging compliance across batch record preparation and review, investigations, training, and cross-functional coordination.You will ensure adherence to GMP, GDP and EHS requirements, manage SOP updates, and serve as a point of contact for work...

CK Group seeks a Quality Auditor to join its CK QLS division in Schachen, working within the Global Development Quality Operations team. The role focuses on GMP documentation review, supporting batch release decisions, and maintaining high standards of GMP compliance.The candidate should have QA/Quality Operations experience in a regulated environment,...

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...

Manufacturing Operator (m/f/d) nemensis ag Vacant since : 15.09.2026 Number of jobs : 1 6105 Schachen LU (LU) 100% From 01.10.2026 Until 15.09.2027 Manufacturing Operator (m/f/d) Your Next Chapter in Biopharma Manufacturing Starts Here Are you ready to bring your hands-on manufacturing skills into a GMP-regulated environment where every batch matters? As a...

ppOur 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. /ppOur...

Specialist GDQ QOS (M/F/D) The Global Development Quality OPS team is responsible to drive or support compliance-based programs and results which include support cross functional projects, solving simple problems, current Good Manufacturing Practices (cGMP) quality initiatives, quality system improvements, quality directives, compliance metrics and...

Quality Auditor CK QLS is recruiting a Quality Assurance Specialist to join the Global Development Quality Operations team at a leading pharmaceutical company in Schachen. This opportunity is suited to a quality-focused professional who enjoys reviewing GMP documentation and supporting compliance within a pharmaceutical environment. Your...

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...

Die B. Braun Medical AG ist eine Tochtergesellschaft der deutschen B. Braun, einer der führenden Hersteller und Lieferanten von Medizintechnikprodukten. Der B. Braun-Konzern beschäftigt über 64'000 Personen in 64 Ländern, davon 1'100 in der Schweiz. Diese sorgen in der Entwicklung, Produktion und dem Vertrieb dafür, dass der Gesundheitsmarkt mit...