About this role
Job Title: Manufacturing Supervisor
Location: Portsmouth, NH (On-site)
As a Manufacturing Supervisor at our Portsmouth site, you will lead daily operations that help manufacture life-changing therapies. You will guide a team and play a key role in delivering high-quality biologics for our customers and patients. This role is based onsite, where working in person supports close, real-time collaboration and the precision needed to manufacture medicines to the highest quality and safety standards.
This role follows a 12-hour day shift schedule from 7:00 AM to 7:00 PM on a rotating schedule of alternating days: two on, two off, three on, two off, two on, three off (repeating cycle).
What you will get
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
Medical, dental, and vision insurance
Opportunities to grow and develop your career
A collaborative and supportive team environment
What you will do
Lead and develop a team of 6+ direct reports to ensure safe, compliant, and efficient operations
Guide and support team members while promoting a strong culture of safety and quality
Coordinate with cross-functional teams to meet production schedules and deliver on time
Review batch records and documentation to support accurate and timely batch release
Train, coach, and develop team members to support performance and growth
Support continuous improvement initiatives and solve operational challenges
Perform administrative tasks such as shift handovers, meetings, and team communication
What we are looking for
5+ years of experience in GMP manufacturing, ideally in biologics or a similar environment
AS or BS degree in a science-related field preferred; equivalent experience will be considered
Strong communication skills with the ability to coach and guide team members
Ability to make sound decisions using logic, critical thinking, and process knowledge
Experience supporting training, onboarding, or staff development activities
Ability to work in a cleanroom environment and follow defined procedures
Ability to collaborate across teams and contribute to a positive work environment
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.
About Lonza
Swiss contract development and manufacturing organization (CDMO) providing biologics, cell, and gene therapy production services.
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