The posting
- Life Sciences - Manufactoring / Production (GMP)
- Contracting
- Teilzeit, 80-100%
- 01.10.2026 - 31.09.2027
- GMP, MES, SOP, Aseptic Fill & Finish, Sterile Manifacturing
Key Facts ####
- Start date: ASAP or by agreement
- Initial duration: 6 months
- Long-term perspective: Extension or long-term employment can be discussed
- Workload: 80-100%
- Location: Basel area, Switzerland
- On-site presence: 4-5 days per week
- Remote work: No fixed home-office day possible during the current project phase
- Work model: Temporary project assignment with potential long-term perspective
- Language: Fluent English required; German is an advantage but not mandatory
- Eligibility: Candidates from Switzerland and EU/EFTA countries are welcome
Your Responsibilities ####
- Support the implementation, qualification and finalisation of a new aseptic pharmaceutical production line
- Work hands-on with filling equipment and isolator technology during qualification, ramp-up and operational stabilisation
- Support commissioning, qualification and validation activities
- Establish, execute and optimise processes within sterile manufacturing
- Monitor manufacturing activities, including preparation, filling, in-process controls and documentation
- Create and revise SOPs and electronic batch records within the MES
- Investigate deviations, technical issues and change requests
- Contribute to troubleshooting and root cause investigations directly at the equipment
- Continuously improve validated manufacturing processes and workflows
- Support internal and external audits as well as regulatory inspections
- Collaborate closely with Manufacturing, Engineering, Quality, Validation and other project stakeholders
Your Profile ####
- Degree, technical qualification or vocational education in Engineering, Pharmaceutical Technology, Production Technology or a related field
- Equivalent professional experience in sterile pharmaceutical manufacturing will also be considered
- Several years of experience in pharmaceutical manufacturing, process engineering, equipment qualification, commissioning or technical production support
- Practical experience in sterile manufacturing or aseptic Fill & Finish
- Experience with vial, syringe, cartridge or other sterile filling equipment is highly desirable
- Experience with isolators, RABS or aseptic barrier systems would be a strong advantage
- Practical experience in equipment implementation, qualification, start-up, troubleshooting or process optimisation
- Experience with SOPs, batch records, MES, deviations or change requests
- Strong technical understanding and willingness to work directly with the equipment
- Independent, pragmatic and solution-oriented working style
- Fluent English is essential
- German is an advantage but not required
- Willingness to work on-site four to five days per week
- EU/EFTA nationality or existing Swiss work authorisation
What You Can Expect ####
- A technically challenging project within a sterile pharmaceutical manufacturing environment
- A key role in the qualification, ramp-up and operational stabilisation of a new aseptic production line
- Direct involvement with filling equipment, isolator technology and manufacturing processes
- Close collaboration within an experienced, multidisciplinary project team
- A dynamic working environment with short decision-making paths and a strong hands-on culture
- The opportunity to discuss an extension, long-term collaboration or permanent position
- The opportunity to build or continue a career in Switzerland, one of Europe-s leading locations for pharmaceutical, biotechnology and medical technology



