USP Manufacturing Team Leader
Thermo Fisher Scientific (Schweiz) AG
Lengnau
Key information
- Publication date:27 January 2026
- Workload:100%
- Place of work:Lengnau
Job summary
Join Thermo Fisher Scientific, a leader in science innovation. Enjoy a dynamic work environment and competitive benefits.
Tasks
- Lead a manufacturing team for recombinant product production.
- Support project teams in new production line validation.
- Ensure adherence to GMP and safety standards in operations.
Skills
- Bachelor's/Master's in relevant field with 5-7 years GMP experience.
- Strong leadership skills with team development experience.
- Knowledge of automated biotech processes and operations.
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Work Schedule
Rotational days/weekends
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Job Description
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
Purpose
- This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
- This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
- This position supports New Product Introduction for recombinant products
Responsibilities
- Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule, shift rotations
- Lead and develop team members in order to run areas robustly and smoothly, ensuring appropriate succession planning
- Participates in defining robust process parameters during routine manufacturing campaigns
- Build cross functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Tachnology, Engineering, Validation, and other relevant functional areas
- Ensures implementation of and adherence to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.
- Ensures contribution of their interpersonal unit to continuous quality improvement initiatives and deviation reporting and follow-up.
- Ensures implementation of and adherence to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
- Ensures contribution of their interpersonal unit to EHSS initiatives and issues as well as near miss reporting and follow-up.
Qualifications
- Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
- 5-7 years successful experience in pharmaceuticals operations in a GMP relevant environment
- The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
- Good knowledge and competence in the field of automated processes
- Experience in leading teams
- Language: English or German
- Shift work is expected
- On-call support