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Training Specialist GMP
vor 3 Monaten
Flexsis is a Swiss company born of the merger between Interima and Global Personal Partner, two leading recruitment companies in our country.
This partnership makes us a major player in recruitment in Switzerland, offering extensive expertise throughout the country. Whichever region of Switzerland you're in, Flexsis's nationwide network means it will be there to support you.
For our leading client in Lengnau Bern, we are looking for a motivated and reliable (m/w/d)
Training Specialist GMP 100%
AUFGABENBESCHREIBUNG:
- Training Leadership: Act as the primary training leader within the operations team.
- Training and Onboarding Management: Develop and oversee training and onboarding programs in manufacturing, including curriculum design, on-the-job training, and trainer mentorship. Ensure training concepts are compliant with regulatory standards.
- Technical Support: Provide technical assistance for critical process activities, working closely with other departments, especially MSAT. Manage and resolve training-related manufacturing deviations.
- Representation: Serve as the DS Manufacturing department representative in cross-functional teams and with external stakeholders, including customers and regulatory authorities. Participate in technology transfers.
- Production Equipment and Systems: Assist in the design, procurement, and implementation of production equipment and automation systems, ensuring they meet process requirements and comply with cGMP standards.
- Process Development and Validation: Support the commissioning, qualification, development, and validation of production processes.
- Manufacturing Excellence: Lead initiatives to enhance manufacturing excellence, ensuring robust and efficient operations.
- Cross-functional Collaboration: Build strong working relationships with other support functions such as Quality Assurance, Quality Control, Manufacturing, Engineering, Validation, and other relevant areas.
- Educational Background: Bachelor's or Master's degree in Chemistry, Biochemistry, Biotechnology, Biology, or Food Science.
- Over 10 years of successful experience in pharmaceutical operations within a GMP-regulated environment.
- Proficiency in biotech processes, with additional experience in sterile processes, single-use equipment, or CIP/SIP processes.
- Fluency in both German and English, both spoken and written.
- Willingness to perform on-call duties and travel up to 15%.
- Experience working in a matrix organization.
- Prior experience with automated technology is highly advantageous.
Our client offers you attractive employment conditions and benefits:
- Shift allowances
- Parking spaces
- Contribution to the health insurance
- Staff restaurant
- 25 days vacation plus additional days
- Rekachecks
- Employee benefits
Are you interested and would you like to seize this opportunity? Then we should definitely get to know each other Simply click on "Apply now" and we look forward to receiving your complete application documents.