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Supervisor, GMP and Technical Training

Job in Houston, Harris County, Texas, 77246, USA
Listing for: Lonza
Apprenticeship/Internship position
Listed on 2026-10-17
Job specializations:
  • Manufacturing / Production
    Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 110000 USD Yearly USD 80000.00 110000.00 YEAR
Job Description & How to Apply Below

The actual location of this job is in Houston, TX, US. Relocation assistance is available for eligible candidates and their families, if needed.

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.

What you will get:
  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • A variety of benefits dependent on role and location.
  • 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 GMPdocumentation 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 auditsas 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 if 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
  • 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
About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences?
  • Take ownership, step forward, and enjoy meaningful responsibility
  • Love solving problems and thrive in a complex, fast-moving environment
  • Are curious, always looking to learn and improve
  • Work collaboratively, contributing to something bigger than yourself
  • Are motivated to make a difference through work that impacts customers and their patients
Why Lonza:

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters.

We are the makers of the medicines of tomorrow.

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