SwissCo Services AG
Bad Aibling
Engineer (m/f/d) Qualification
- 04 September 2026
- 100%
- Permanent position
- Bad Aibling
Job summary
Join Aenova, a leader in pharmaceutical manufacturing and development! Contribute to patient health in a supportive work environment.
Tasks
- Conduct risk analyses and create qualification plans effectively.
- Plan and execute qualifications, coordinating with various departments.
- Ensure compliance by overseeing qualification activities and documentation.
Skills
- Degree in engineering or related fields; QA experience preferred.
- Strong problem-solving skills and proactive mindset are essential.
- Excellent English skills and proficiency in MS Office required.
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About the job
Would you like to make a valuable contribution to the health of patients? And take responsibility to achieve something truly meaningful? 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 Bad Aibling is a competence centre for blister packaging and effervescent tablets.
Your area of responsibility
Creation of risk analyses and qualification test plans
Planning and execution of qualifications including coordination of the involved departments
Technical control and acceptance of qualification activities as well as documentation of equipment acceptance
Creation, review, maintenance and evaluation of quality-relevant documents
Creation, monitoring and evaluation of key figures, statistics and trend analyses to control qualification quality
Support and, if necessary, conduct training within the area of responsibility
Presentation of qualification agendas during regulatory inspections and customer audits; support during customer and regulatory audits
Project participation in cross-departmental initiatives
Collaboration and technical guidance in planning and implementing company-specific quality objectives
Your profile
Successfully completed technical degree (e.g. pharmaceutical or process engineering, chemical engineering)
Experience in the quality assurance area of a pharmaceutical company
Relevant expertise in the field of qualification
Strong can-do spirit combined with a very high quality standard
Proactive working style and a solution-oriented approach to problems
Good IT skills
Solid MS Office skills as well as very good English skills, both written and spoken
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, I – Vanessa Handrock / Human Resources – am happy to assist you: +49 8061 931-105
