QA Manager (m/f/d) 100%
SwissCo Services AG
Sisseln
Key information
- Publication date:03 November 2025
 - Workload:100%
 - Contract type:Permanent position
 -  Place of work:Sisseln
 
Job summary
Join Aenova, a global leader in pharmaceutical manufacturing, to make a valuable contribution to patient health. Enjoy a dynamic work environment with opportunities for personal impact.
Tasks
- Manage the quality management system according to ISO 9001 standards.
 - Plan and conduct customer and authority audits effectively.
 - Support CAPA and Deviation Management and handle complaints.
 
Skills
- Degree in a scientific field; experience in quality assurance in GMP environments.
 - Fluent in German and English, both spoken and written.
 - Strong analytical skills with a structured, organized work approach.
 
Is this helpful?
Do you want to make a valuable contribution to the health of patients? And take responsibility to make a truly meaningful impact? Then we look forward to hearing from you! Excellence beyond manufacturing – that is what we stand for at Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 locations. Our site in Sisseln is a competence center for complex and innovative solids.
Area of responsibility
Responsibility for the quality management system (QMS) according to ISO 9001 as well as creation and review of quality reports, SOPs, and process instructions
Planning, conducting, and follow-up of customer and authority audits
Qualification and evaluation of suppliers and service providers, including conducting on-site audits
Participation in the control and further development of CAPA and deviation management as well as support in complaint management
Participation in the maintenance and further development of document and training management
Conducting training sessions within your area of responsibility to promote quality awareness
Participation in quality-relevant projects within the Aenova group
Your profile
Completed scientific studies (e.g., pharmacy, chemistry, biotechnology, biology, etc.)
Professional experience in quality assurance of a manufacturing company in a GMP environment (e.g., pharmaceutical or food sector)
Very good German and English skills, both spoken and written
Good MS Office skills, especially Word and Excel
High resilience, initiative, and team player
Analytical and networked thinking ability
Structured and organized working style with the ability to set changing priorities
Your motivation
Are you looking for new challenges in a competitive environment? And do you want to tackle them creatively and independently?
Do you prefer a "get-it-done" culture and think more in solutions than in problems?
What are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!
If you have any questions, Human Resources is available at: +41 62 866 42 42