Midscale Manufacturing Supervisor (Life Sciences)

TL;DR

Midscale Manufacturing Supervisor (Life Sciences): Leading safe and compliant daily operations in a cGMP manufacturing suite with an accent on team leadership, batch record accuracy, and production goal attainment. Focus on troubleshooting equipment issues, coaching operators, and driving continuous improvement in a cleanroom environment.

Location: On-site in Portsmouth, NH, USA

Company

Global leader in life sciences manufacturing, specializing in the production of breakthrough medicines and therapies.

What you will do

• Lead daily manufacturing operations within a cGMP suite to ensure safety and compliance.
• Plan production schedules and assign tasks to meet organizational goals.
• Review batch records and logbooks for high accuracy and clarity.
• Coach and develop operators through continuous training and feedback.
• Collaborate with cross-functional teams to resolve operational obstacles.
• Troubleshoot equipment and process issues while supporting SOP updates.

Requirements

• 5–10 years of experience in a GMP or manufacturing environment.
• AS/BS degree in a science field (or HS diploma with equivalent experience).
• 1–4 years of supervisory or team-leading experience preferred.
• Ability to work in cleanrooms and lift up to 50 lbs.
• Must be able to work the rotational night shift (7:00 PM – 7:00 AM).

Culture & Benefits

• Inclusive and ethical workplace with a dynamic working culture.
• Medical, dental, and vision insurance.
• Compensation programs recognizing high performance.
• Additional pay for night and weekend shifts.