Sisseln
Senior Galenic Formulation Technician (m/f/d) 100%
- 01 July 2026
- 100%
- Permanent position
- Sisseln
Job summary
Join Aenova as a Specialist in Galenic Development in Sisseln! Contribute to patient health in a supportive, innovative environment.
Tasks
- Conduct technical trials and produce GMP-compliant batches.
- Assist in process validations and scale-up activities.
- Ensure compliance with GMP and safety regulations.
Skills
- Completed training as a Chemist or Pharma Technician with experience.
- Strong practical skills and initiative in work processes.
- Good knowledge of MS Office and fluent in German and English.
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About the job
Specialist in galenic development with many years of experience (m/f/d) 100%
We are looking for a committed and flexible individual for our site in Sisseln (AG).
Do you want 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 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 Sisseln is a competence centre for complex and innovative solids.
Area of responsibility
Independent execution of technical trials as well as production of trial mixtures and GMP-compliant batches for clinical studies and approval projects.
Participation in process validations, scale-up activities and production of test and validation batches.
Operation, setup, conversion and monitoring of production equipment as well as in-process control (IPC) devices in the pilot plant in compliance with GMP and safety requirements.
Recording, maintenance and adjustment of manufacturing instructions in the ERP system according to specified specifications and release processes.
Sampling, labelling, management and archiving of retention samples from trial, validation and GMP batches in compliance with applicable GMP requirements.
Creation, revision and maintenance of standard operating procedures (SOPs), manufacturing instructions and other manufacturing-specific documentation.
Ensuring complete and GMP-compliant documentation of all manufacturing and trial steps.
Compliance with applicable GMP, safety, hygiene and quality regulations in the pilot plant.
Collaboration with the Analytical Development team
Your profile
Completed training as a chemical technician or pharmaceutical technician with analytical experience
Several years of GMP experience
Enjoyment of practical work (conducting trials)
Solid IT skills (MS Office)
Good German and English skills, spoken and written
Initiative, commitment and willingness to learn
Flexibility, independent working style and resilience
Willingness to work night shifts for one week during certain project phases (approx. 1-3 times per year)
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? We will be happy to explain our corporate benefits in a personal conversation!
If you have any questions, Human Resources is happy to assist you at: Tel: +41 62 866 42 42
