Review and release of batch records in cooperation with FvP
Processing of deviations, complaints as well as CAPAs and GMP documents
Create, modify, and release manufacturing instructions, SOPs, and manufacturing documentation
Maintaining and optimizing the quality management system, including creating master batch documents
Contact person for quality-related questions within the scope of internal and external projects
Preparation of authority audits, inspections
Your profile
Completed studies (Uni, FH) in chemistry, pharmacy or similar
3-5 years of experience in quality assurance within a chemical/pharmaceutical environment.
Sound GMP know-how
Reliable and independent personality with exact and structured way of working
You speak German and English fluently
Your benefits
Dynamic environment in which personal responsibility and independence are emphasized
Flat hierarchies and short decision-making paths
Growing company with long-term development opportunities
Our customer
Our client is a leading and recognized service provider in the chemical-pharmaceutical industry with around 100 employees. The owner-managed company specializes in the development and production of active ingredients and end products and primarily produces and packages tablets and capsules using modern machinery. Place of work: Basel region
