Manager QA Projects (a), 100%

The role of Manager QA Projects (a) at Bachem involves leading quality assurance efforts within product-related projects. Bachem is a global company focused on the development and manufacture of peptides and oligonucleotides, serving pharmaceutical and biotechnology industries with a range of products and services. The main day-to-day responsibilities include representing QA in various projects, making decisions on QA-relevant topics, and coordinating tasks within QA departments. The role also involves acting as a key contact for other departments regarding cGMP compliance and troubleshooting, defining control and lifecycle strategies, and reviewing GMP documents. Additionally, the Manager QA Projects will serve as a contact point for both internal and external stakeholders on QA-related matters. To qualify for this position, candidates must have a Master's or Ph.D. in chemistry, biology, pharmacy, or a related technical field, along with at least 2 years of professional experience in project management and quality assurance within the chemical/pharmaceutical industry. A strong understanding of QA topics, solid cGMP knowledge (EU-GMP, FDA), and experience in supporting process validations, including risk management, are essential. Nice-to-have skills include being a structured and solution-oriented professional with strong communication skills, capable of clearly conveying complex topics. The role is based in Bubendorf, Switzerland, where Bachem offers a dynamic and rapidly growing work environment with internal development and training opportunities. The company provides flexible working hours, home office days, and a range of benefits, including a company-run daycare center, pension fund contributions, and access to various sports activities. What the role asks for: - Master's or Ph.D. in chemistry, biology, pharmacy, or a comparable technical field. - 2 years of professional experience in project management and quality assurance within the chemical/pharmaceutical industry. - Strong understanding of QA topics. - Solid cGMP knowledge (EU-GMP, FDA). - Experience in supporting process validations including risk management. - Excellent verbal and written communication skills in both German and English.