Bubendorf
QA Associate - Batch Compliance (a) 100%
- 22 October 2026
- 100%
- Permanent position
- 4416 Bubendorf
About the job
Bachem is a publicly listed technology company focused on peptide chemistry, offering a comprehensive range of services for the pharmaceutical and biotechnology industries. Bachem specialises in the development of innovative, efficient manufacturing processes and the reliable production of peptide-based pharmaceutical active ingredients. An extensive catalogue of biochemicals for research purposes and exclusive customer syntheses complement the offering. With headquarters in Switzerland and branches in Europe and the USA, the company operates worldwide and possesses the industry’s greatest experience and expertise. In collaboration with its customers, Bachem places the highest value on quality, innovation, and partnership.
QA Associate - Batch Compliance (a) 100%
To drive our continuous organic growth, we are constantly seeking highly qualified professionals. To strengthen our quality assurance team, we are looking for motivated Associates QA - Batch Compliance (a) for a 100% position.
Your tasks:
- Review of GMP manufacturing documentation on paper or in the electronic PAS-X system for the release of our active ingredients
- Checking documentation of intermediate and final stages for GMP compliance and conformity with internal regulations
- Discussing discrepancies with the executing personnel in the production areas and agreeing on necessary corrective actions
- Determining customer eligibility to purchase our active ingredients, reviewing shipping documentation of our GMP products
- Implementing GDP (Good Distribution Practice) guidelines in the provision, handling, and distribution of our GMP products
Your profile:
- Vocational training as a chemical laboratory technician, chemical-technical assistant (CTA), chemical and pharmaceutical technologist, or comparable qualification
- At least 2 years of professional experience within the chemical/pharmaceutical industry, preferably in a GMP environment or in the control of GMP manufacturing documentation
- You are accustomed to creating, reviewing documents and enforcing corrective actions. Experience with electronic quality management systems is an advantage
- You are an independent and responsible person with a careful and team-oriented working style and a high understanding of quality assurance aspects
- You have very good oral and written expression in German and can demonstrate good English skills
- You have interest and experience with electronic systems for batch documentation (MES) and are confident in using Microsoft Office. SAP knowledge is an advantage
Our offer:
- A dynamic and rapidly growing work environment with internal development opportunities
- Flexible working hours possible
- Employee support through numerous internal and external training opportunities
- 60% coverage of pension fund contributions by Bachem AG as well as the possibility for additional voluntary pension provision with our savings plan
- Access to the Swibeco benefits platform with discounts at external partners
- Fresh, healthy, and varied food in our staff restaurant
- Various free sports activities on the Bachem campus
Would you like to drive innovation forward with us?
Have we piqued your interest? Then we look forward to receiving your complete application documents via our application portal.
Learn more about the Bachem Group and be inspired by our inspiring working environment at our location in Bubendorf!