Supervisor, GMP and Technical Training
- Location
- Houston, TX
- Listed
- 3 days ago
Houston, TX
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.
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 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
- 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
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?
From Lonza's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
Rolev.ai is a job search and application tool for US job seekers. For this Supervisor, GMP and Technical Training role at Lonza, it shows how your resume fits, tailors your resume to the posting, and prepares the application for you to review.
See how you fit
Openings from employer career sites are ranked against your whole resume—and searchable inside Claude, ChatGPT, and Cursor via Rolev.ai MCP.
Tailor without inventing
Every change to your resume is checked against your original. New experience goes in only with your yes—zero fabricated claims.
Draft the full kit
Tailored and Full Match resumes, role-specific cover letters, and answers to employer screening questions are prepared in seconds.
1-Click Extension Autofill
The Chrome extension fills the employer's Greenhouse, Workday, Lever, or Ashby form in 1 click. You review it and press Submit.
Common questions
Where is the Supervisor, GMP and Technical Training job at Lonza located?
This Supervisor, GMP and Technical Training position at Lonza is located in Houston, TX. Always check Lonza's application page for specific state eligibility or relocation policies.
How do I apply for the Supervisor, GMP and Technical Training position at Lonza?
This listing links directly to Lonza's Workday application page. You can apply directly on Lonza's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.