Manufacturing Engineering Team Lead | Medical Devices | Switzerland | Competitive Salary I am partnering with an innovative medical device manufacturer to appoint a Team Leader within their Manufacturing Engineering function. The company operates in an
An innovative company with a global presence Proven track record in batch record review About Our Client For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking
International pharma company 18 months contract with extensionoption About Our Client Our client is a well-established organization within the pharma industry, renowned for delivering innovative solutions and maintaining a strong commitment to quality and compliance. Operating
The Commissioning & Qualification Engineer role in the Metrology & Validation department, oversees and supports the qualification of analytical instrumentation and Computer Systems projects within the GMP environment. Responsibility of this function is to maintain the
DMD Solutions is a consulting company specialized in aerospace design and RAMS engineering, offering project outsourcing and engineering tool development. Our clients are manufacturers and maintainers of aeronautical products located in Europe. We help them achieve
Operator for Biotech Support Operations For one of our clients, an international pharmaceutical company, we are seeking an Operator for Biotech Support Operations . General Information: Start date: ASAP (high urgency) End Date: 1 year Home
DMD Solutions is a consulting company specialized in aerospace design and RAMS engineering, offering project outsourcing and engineering tool development. Our clients are manufacturers and maintainers of aeronautical products located in Europe. We help them achieve
Operator for Biotech Support Operations For one of our clients, an international pharmaceutical company, we are seeking an Operator for Biotech Support Operations . General Information: Start date: ASAP (high urgency) End Date: 1 year Home
The GMP 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
The Batch Record Reviewer supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation meets ALCOA+ , GDP , and GMP expectations. As part of the Manufacturing Operational Excellence team, this
Overview Are you passionate about quality, precision, and working in a GMP-regulated environment? We are currently seeking a detail-oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment.
About Our Client For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking a Batch Record Review Specialist (m/f/d). In this role, you will support clinical biologics
Für unseren Kunden, einem führenden Pharmaunternehmen in der Nähe von Luzern, suchen wir ab 1. Juli 2026 eine engagierte und motivierte Persönlichkeit als Dokumentationsspezialist/in, 100 % (w/m/d) Diese Position arbeitet eng mit den Teams in der