Management and further development of the teams in Quality Assurance and Qualification & Validation with several employees
Compliance with the Pharmaceutical Quality System (PQS) and GMP guidelines
Management and processing of deviations, changes, complaints and CAPAs
Supporting the FvP in reviewing batch records and releasing quality-relevant documents (SOPs etc.)
Ensuring GMP compliance and improving quality-related processes in terms of efficiency
Preparation and implementation of customer audits and inspections by authorities (Swissmedic)
Continuous further development of the quality management system, anchoring the concept of quality in the organization and conducting employee training courses
Your profile
Completed scientific studies (chemistry, pharmacy, biology or similar)
Many years of experience in quality assurance in a manufacturing pharmaceutical company under GMP conditions
Experience in an aseptic manufacturing plant is an advantage
At least 3 - 5 years of experience in personnel management of a small team
Open, communicative and assertive personality with a hands-on mentality
You are characterized by resilience, initiative and a structured way of working
Fluency in German and English is essential
Your advantages
Very good training period with exciting development prospects
Active support for further training
Versatile and varied field of activity with a lot of personal responsibility
Our customer
Our client is a long-established company that specializes in the manufacture and filling of chemical-pharmaceutical products. The company has sites in Germany and Switzerland and is active in all areas from formulation and production to filling and logistics. Place of work: Lucerne region
