Supervisor, Media Manufacturing
Senior Supervisor, Media Manufacturing
Location: This position is based at our Walkersville, MD site and is a full-time role with a Monday–Friday schedule from 8:00 a.m. to 5:00 p.m. Relocation assistance is supported for this role.
The Supervisor, Media Manufacturing is responsible for overseeing daily operations within the powder media manufacturing area, ensuring compliance with cGMP standards and maintaining a safe work environment. This role leads a team to achieve key performance indicators, drive continuous improvement initiatives, and ensure adherence to manufacturing procedures. The Supervisor partners closely with Quality Assurance to guarantee that all products meet quality system requirements and applicable regulatory standards.
What you will get:
The full-time base annual salary for this on-site position is expected to range between $89,000 to $143,000. 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:
Supervise and coordinate daily manufacturing activities to meet production schedules for Powder Manufacturing Production Department (PMPD).
Provide on-the-floor leadership through coaching, guidance, and training of operators.
Set priorities and allocate resources to ensure timely completion of tasks; collaborate with other team leaders and support functions.
Review and revise batch records, SOPs, and forms for GMP compliance; ensure timely review of completed batch records.
Investigate and resolve manufacturing deviations, CAPAs, and customer complaints promptly.
Manage employee performance through clear expectations, documentation, and development plans.
Ensure production equipment is maintained in optimal condition, coordinate with support teams for sourcing, repairs, and retirement of equipment.
Participate in internal and customer audits, providing tours and audit support as needed.
Support new product introductions, cross-functional projects, and process improvement initiatives.
Perform other duties as assigned.
What we are looking for:
Minimum 7 years of management experience leading small to medium-sized teams in a manufacturing environment.
Experience with aseptic practices and cleanroom operations (required).
Strong knowledge of GMPs, SOPs, and regulatory compliance.
Understanding of biology and chemistry principles.
Proficiency in computer applications; strong organizational, planning, and record-keeping skills.
Ability to manage multiple projects and priorities effectively.
Excellent communication, negotiation, and team-building skills.
Demonstrated ability to coach, delegate, and motivate team members while fostering a positive work environment.
Strong problem-solving skills and a proactive approach to continuous improvement.
Preferred: Experience in powder media manufacturing (PMPD) or similar powder-focused production environments.
Open to candidates from related industries such as food & beverage, cosmetics, or other powder-based manufacturing sectors.
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.
