Contact person for quality-related questions within the scope of internal and external projects
Create, modify, and release manufacturing instructions, SOPs, and manufacturing documentation
Collaboration on change control as well as review and approval of batch records
Processing of deviations, complaints as well as CAPAs and GMP documents
Maintain and optimize the quality management system
Carrying out supplier qualifications as well as cooperation in qualification and validation projects in production
Preparation of authority audits, inspections as well as conducting trainings
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 advantages
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 130 employees. As a specialist in custom synthesis, the company offers a broad portfolio ranging from process development and scale-up to production and accompanying analytical development. Place of work: Northwestern Switzerland region
