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....

pBachem 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. /ppApplicants should hold a Master’s degree or PhD in Chemistry or related field, with...

Bachem in Vionnaz, Switzerland, is seeking a Technical Author to join our TechOps team on a full-time basis. You will create and maintain GMP manufacturing documentation, support technology transfer projects, and translate process knowledge into compliant, manufacturing-ready records.You will work closely with Process Scientists, laboratories, Manufacturing...

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...

pGXP 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. /ppIdeal candidates have 5–10 years in pharma/biotech with strong Fill Finish aseptic experience...

Bachem Holding AG is establishing a new site in Stein, Northwestern Switzerland, where the Technical Author will ensure GMP documentation quality for API manufacturing. You will work across Manufacturing, QA, Regulatory Affairs, and R&D to support tech transfer and process scale-up.The role requires a strong GMP documentation background, German and English...

pbagap2 /b 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. /ppAs a consultant, you will have to support our clients in the realization of their projects on...

ppbagap2 /b 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. /p pAs a consultant, you will have to support our clients in the realization of their projects on...

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...

Bachem is developing a new Sisslerfeld site in Northwestern Switzerland. We seek a QE Manager CSV (a) 100% to lead C&Q/CSV activities, ensure GMP compliance, and oversee qualification of computerized systems across the project lifecycle.The role requires a degree in engineering/chemistry/pharmacy and at least three years in pharma CAPEX CSV projects, with...

agap2 Switzerland is a European engineering and operational consulting group focused on Pharma, Biotechnology, Medical Devices, Energy, and related sectors. As a consultant, you will support clients on site, applying your QA expertise to qualification activities and regulatory compliance.You will review IQOQPQ protocols, maintain documentation, and...

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...

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...

Bachem Holding AG in Bubendorf seeks a Local Head of Technical Operations to lead multiple domains, aligning local priorities with global TechOps. You will manage domain leads, drive process optimization, and support GMP readiness at the site with a strong focus on NCE projects and digital initiatives.You are a senior leader with 10+ years in GMP pharma,...

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...

Bachem Group is expanding with a new site in Sisslerfeld, Northwestern Switzerland, to strengthen API production capacity. We seek a Technical Author to develop, maintain, and assure GMP documentation at our Stein site, interfacing Manufacturing, QA, Regulatory Affairs and R&D.You will translate complex manufacturing processes into compliant documentation,...

pConsultys Suisse is seeking a Quality Systems Specialist (GMP) in Switzerland to support deviations, change controls, documentation management, and risk assessments. You will work with cross-functional teams to uphold GMP compliance and drive quality improvements across the organization. /ppThe role requires a degree in a scientific field and prior GMP...

pZüriPharm AG in the Zurich region is seeking a Quality Manager (100%) to lead quality management activities across materials, production, and documentation, ensuring compliance with GMP and AMBV. /ppYou hold a Master's degree in Pharmacy (or natural sciences) with at least two years of QA/QC experience in pharma, excellent German (C1) and good English, and...

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...

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...