Supervisor, GMP and Technical Training
Lonza
Summary
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
Job description
What you will do
- Design, develop, and deliver instructor-led, hands-on, and on-the-job training programs for manufacturing personnel.
- Qualify and certify manufacturing employees on production processes, aseptic techniques, cleanroom behaviors, equipment operation, and GMP documentation practices.
- Maintain training curricula, qualification matrices, and training records in accordance with regulatory requirements.
- Partner with Manufacturing leadership to identify skill gaps and develop targeted training plans.
- Conduct training effectiveness assessments and implement continuous improvements to training programs.
- Support onboarding of new manufacturing employees through structured learning pathways.
- Collaborate with Subject Matter Experts (SMEs) to develop and revise training materials, job aids, and standard work documentation.
- Support deviation investigations related to training deficiencies and implement corrective actions when required.
- Assist with new product introduction (NPI) activities by developing and delivering training associated with new processes, equipment, and procedures.
- Participate in internal audits, regulatory inspections, and customer audits as a training subject matter expert.
- Monitor training compliance and proactively address overdue qualifications.
- Support both day shift and night shift based on business needs.
- Perform other duties as assigned.
What we are looking for
- Bachelor's Degree in Life Sciences, Biotechnology, or related field
- 5-10 Years of experience in biotech/biopharma laboratory or manufacturing experience preferably in a Cell Therapy manufacturing environment.
- Excellent communication skills (oral and written)
- Excellent Aseptic Technique and Cleanroom Skills
- Ability to perform aseptic gowning on a daily basis
- Computer software skills (i.e. Cornerstone, Microsoft Office, Trackwise)
- Database and spreadsheet creation and maintenance
- Organization, record keeping, and planning skills
- Managing multiple projects, time management skills
- People management and training methods
- Able to assess and recommend training needs and training assignments/requirements/curricula.
- Ability to lead cross-functional consultation on training strategy, strong facilitation and delivery skills, and ability to coordinate complex training initiatives.
- Skilled in coaching, training, and facilitation practices
- Ability to travel at least 20% travel based on site location and or client visits
Requirements
- Bachelor's Degree in Life Sciences, Biotechnology, or related field
- 5-10 Years of experience in biotech/biopharma laboratory or manufacturing experience preferably in a Cell Therapy manufacturing environment
- Excellent communication skills (oral and written)
- Excellent Aseptic Technique and Cleanroom Skills
- Ability to perform aseptic gowning on a daily basis
- Computer software skills (i.e. Cornerstone, Microsoft Office, Trackwise)
- Database and spreadsheet creation and maintenance
- Organization, record keeping, and planning skills
- Managing multiple projects, time management skills
- People management and training methods
- Able to assess and recommend training needs and training assignments/requirements/curricula
- Ability to lead cross-functional consultation on training strategy, strong facilitation and delivery skills, and ability to coordinate complex training initiatives
- Skilled in coaching, training, and facilitation practices
- Ability to travel at least 20% travel based on site location and or client visits
Benefits
- Agile career
- Dynamic working culture
- Inclusive and ethical workplace
- Compensation programs
- Global benefits
- Relocation assistance
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.