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.
- Strong communication, decision‑making, and problem‑solving skills.
- 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.
- 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.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Manager
Education Level
Associate degree
