bach documentation gmp pharma

Proclinical Staffing sucht einen Verpackungsbediener zur manuellen Etikettierung und Verpackung von Medikamenten in klinischen Studien. Sie arbeiten gemäß GMP-, Sicherheits- und Umweltvorschriften und sichern saubere, ordentliche Arbeitsbereiche.Zu Ihren Aufgaben gehören Dokumentation, Qualitätsprüfungen und Zusammenarbeit mit anderen Abteilungen....

Bachem SA in Vionnaz, Switzerland, seeks a Technical Author to join the TechOps team at 1895 Vionnaz (VS). You will create and maintain GMP manufacturing documentation, support technology transfer and new product introductions, and digitalize manufacturing records.Applicants should hold a Master’s degree or PhD in Chemistry or related field, with 3–5...

Bachem is a Basel-based technology leader in peptide chemistry, offering GMP documentation and manufacturing excellence. The Technical Author (a) 100% role sits at the interface of Manufacturing, QA, Regulatory Affairs and R&D, contributing to technology transfer and process improvement at the new Sisslerfeld site.You will develop, maintain, and ensure...

The Bachem Group is expanding with a new site in Sisslerfeld, Northwestern Switzerland, and seeks a Technical Author to develop, maintain, and ensure GMP documentation for API manufacturing at the Stein site. You will interface Manufacturing, QA, Regulatory Affairs, and R&D to support tech transfer, scale-up, and continuous improvement of processes.The role...

GXP CONSULTING Switzerland is seeking a Plant Engineer to join our Bern-based life sciences team. You will drive engineering activities from concept through start-up, developing robust documentation and coordinating with production, QA, and validation groups.Ideal candidates have 5–10 years in pharma/biotech with strong Fill & Finish aseptic experience and...

agap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.As a consultant, you will have to support our clients in the realization of their projects on site by...

agap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors. As a consultant, you will have to support our clients in the realization of their projects on site by...

agap2 Switzerland is seeking a CQV Engineer to support GMP pharma/biotech projects on-site from installation to validation. You will work with major clients to ensure compliant, efficient commissioning and qualification processes.Responsibilities include executing DQ/IQ/OQ/PQ, meeting milestones, supervising vendors, and producing validation documentation....

agap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors. As a consultant, you will have to support our clients in the realization of their projects on site by...

Nemensis AG Schweiz is seeking a Manufacturing Operator (m/f/d) for a temporary placement to support the Drug Substance Bioprocess team in a GMP environment. You will set up and operate manufacturing equipment, manage materials, and ensure documentation and compliance on the shop floor.The role requires at least 1 year in pharma/biotech, strong GMP...

Wählen Sie aus, wie oft (in Tagen) Sie eine Benachrichtigung erhalten möchten: Senior Documentation Manager (a) (80 -100%) für Engineering Services Bachem ist ein führendes, innovationsgetriebenes Unternehmen, das sich auf die Entwicklung und Herstellung von Peptiden und Oligonukleotiden spezialisiert hat. Mit einem umfassenden Dienstleistungsangebot...

Bachem AG in Bubendorf, Switzerland, seeks an experienced Manager QA (a), 100% temporary for 12 months, to strengthen External Supply Quality Assurance. You will ensure GMP compliance across the external supply network, work with suppliers, contract manufacturers and cross-functional teams, and help maintain quality, safety and reliability of sourced...

DescriptionWe are looking for a Technical Writer to strengthen our GMP documentation capabilities. In this role, you will support lab operations by creating clear, compliant, and structured documentation, enabling efficient and audit-ready processes across SOPs, QEs, and CAPAs. ResponsibilitiesCreate, update, and standardize SOPs, work instructions, and...

Bachem is expanding with a new site in Sisslerfeld, Northwestern Switzerland, seeking an experienced Commissioning & Qualification Engineer to lead C&Q activities on global capital projects. You will shape standards, manage from concept to handover, and drive lean, agile improvements across sites.Ideal candidate has 10+ years in pharma/biopharma, strong GMP...

Bachem, a leading peptide-focused biotech company, seeks a MES System Engineer (80–100%) to drive full lifecycle management of the PAS-X MES at a new Northwestern Switzerland facility. You will align MES with Pharma 4.0, collaborate across functions, and ensure GMP-compliant operation through start‑up and commercial manufacturing phases.The role...

Incyte Corporation in Vaud, Switzerland seeks a QC Lab Coordinator to support Quality Control through administration, documentation, and sample handling. You will manage samples, assist in procurement, track reagents, and ensure records align with the quality system.Candidate should have 1–3 years in pharma or biotech with GMP exposure, strong...

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...

Pharma client in Visp seeks an EI&C PI Engineer to administer PI Data Archive, AF/EF, and analytics, while integrating with DeltaV, MES, and enterprise systems. The role focuses on data integrity, GMP/GxP documentation, and cross-functional collaboration with Automation, Manufacturing, and IT teams.Responsibilities include designing interfaces, developing...

Swisslinx is seeking an Associate III – Integrated Downstream Quality Operations in Solothurn, Switzerland. You will support QA activities across downstream GMP manufacturing and equipment, collaborating with Manufacturing, Process Engineering, Manufacturing Sciences and Automation teams.The role requires strong QA experience in GMP biotech/pharma...