QA Specialist (m/f/d) 80-100% - Aenova Group
Kirchberg SG
Key information
- Publication date:18 June 2025
- Workload:80 – 100%
- Contract type:Internship
- Place of work:Kirchberg SG
Job summary
Join Aenova, a leading global contract manufacturer in pharmaceuticals. Make a meaningful impact on patient health!
Tasks
- Handle change control procedures and customer complaints effectively.
- Conduct product batch release and assess production deviations.
- Support QA trainees and create necessary documentation.
Skills
- Scientific education or relevant experience in quality management required.
- Strong knowledge of pharmaceutical regulations and documentation.
- Proficient in MS Office and SAP, with excellent language skills.
Is this helpful?
Do you want to make a valuable contribution to the health of patients? And do something truly meaningful independently? Then we look forward to seeing you! Excellence beyond manufacturing – that’s what we stand for as 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 Kirchberg SG is a competence center for the development and production of softgel capsules.
Responsibilities
DHC Business Admin - Document Module (DM), Training Module (TM), Measures Module (MM), Change Control Module (CC), Deviation Module (DEV)
Assessment, coordination, and completion of change requests (Change Control Procedure)
Processing and coordination of customer complaints and preparation of the Investigation Report
Product Batch Release (release/non-release) in delegation of the Qualified Person (FvP) and making the usage decision in SAP (QA11) as well as assessing deviations during production and analytics.
Basic Block I-III training responsibility, supervision of QA interns
Data collection from the own area of responsibility for the monthly "Q-KPI / KCI Reporting" and the annual "Management Review"
Preparation of SOPs/AAs/FBs
Qualified internal auditor and participation in customer and authority audits
Your Profile
Completed scientific education (PTA, CTA, or similar) or solid professional experience in the field of quality management or relevant studies
Experience in the pharmaceutical sector
Experience in the food technology environment is an advantage, especially in regulations for dietary supplements and dietary foods
Knowledge of relevant legislation and regulations
Understanding of documentation and proficient use of standard software (good MS Office skills), SAP knowledge is an advantage
very good German / English skills in spoken and written
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 in solutions rather than problems? What are you waiting for?
If you have any questions, Human Resources is available at: +41 71 932 62 62
