Lead Technician Media – 2nd Shift
Location: This position is based in our Walkersville, MD office. The typical work schedule is Monday through Thursday, 2:00 PM–12:00 PM EST.
What you will get:
The full-time base annual salary for this position is expected to range between $72,000 to $114,000. In addition, below you will find a comprehensive summary of the benefits package we offer:
Performance-related bonus.
Medical, dental and vision insurance.
401(k) matching plan.
Life insurance, as well as short-term and long-term disability insurance.
Employee assistance programs.
Paid time off (PTO).
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
What you will do:
As a Lead Technician, you will play a key role in supporting production operations within a Powder or Liquid Media manufacturing environment. This role combines hands-on manufacturing responsibilities with team leadership, ensuring compliance with GMP standards and operational excellence in a fast-paced, safety-focused setting.
Execute aseptic processing in a cleanroom environment in accordance with SOPs
Set up, operate, and maintain production equipment
Complete manufacturing documentation accurately and in real time
Perform personal and environmental monitoring
Gown and work in aseptic conditions
Clean production tanks and associated equipment
Formulate bulk production batches and stock solutions
Process batches using LFBSC (Laminar Flow Biological Safety Cabinet)
Conduct integrity testing on sterilizing filters
Prepare and assemble materials for autoclaving
Perform material transfers, including de-boxing, disinfecting, and staging cleanroom materials
Support drum filling operations as needed
Maintain production inventory within assigned areas
Ensure general upkeep and preventative maintenance of equipment and facilities
Review and approve batch records and production documentation
Stay current with all required training
What we are looking for:
Prior experience in a GMP-regulated manufacturing or cleanroom environment preferred
Strong attention to detail with the ability to follow complex procedures
Solid written and verbal communication skills
Support updates to SOPs, batch records, and related documentation
Investigate and document deviations in compliance with GMP standards
Ability to work independently and collaboratively in a team environment
Adaptable and proactive in a fast-paced, high-volume setting
Willingness to work onsite (minimum four days per week)
Training Schedule: First Shift – 6:30 AM to 5:00 PM, Monday through Thursday
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 offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. 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? Apply now.