Manufacturing Supervisor (Days - A Shift)
Lonza•Portsmouth, NH
•Onsite
About The Position
You will lead a manufacturing team producing therapeutic proteins in a cGMP environment at our Portsmouth, NH site. In this on-site role, you will coach operators, ensure quality and safety, and deliver production results that support life‑changing medicines.
Requirements
- AS or BS degree in a science‑related field; a high school diploma with relevant experience will be considered.
- Ability to work a day‑shift rotating schedule from 7:00am–7:00pm, following a 2 on, 2 off, 3 on, 2 off, 2 on, 3 off repeating pattern.
Nice To Haves
- Manufacturing experience in a GMP environment preferred.
- Previous people‑leadership or supervisory experience preferred.
- Strong communication, decision‑making, and problem‑solving skills.
- Experience in biological manufacturing or cleanroom operations preferred.
- Familiarity with electronic batch records and technical documentation.
Responsibilities
- Lead safe, high‑quality daily manufacturing operations in your assigned production suite.
- Coordinate with cross‑functional teams to meet production schedules on time.
- Coach and support team members to ensure full compliance with GMP and quality systems.
- Review batch records and logbooks for accuracy, clarity, and completeness.
- Train, develop, and provide performance feedback to operators through regular coaching.
- Support documentation activities, including deviations, SOPs, and technical writing.
- Promote housekeeping, 6S, daily management practices, and continuous improvement.
Benefits
- Medical, dental and vision insurance.
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What This Job Offers
Job Type
Full-time
Career Level
Manager
Education Level
Associate degree
