Aseptic GMP Manufacturing Supervisor

PCI Pharma Services; Bedford (NH); On-site; USD 95,000 - 120,000; Full time

Job summary

PCI Pharma Services seeks a Manufacturing Supervisor to lead an aseptic and medical device manufacturing team in Bedford, NH. The role requires hands-on leadership across GMP operations, ensuring safety, quality, and efficient production on a 2-3-2, 12-hour shift schedule beginning January 2026.

You will drive staffing, coach performance, and collaborate with QA, Regulatory, and cross‑functional groups to meet capacity and quality targets while mitigating risks and implementing improvements.

Qualifications

• Minimum High School Diploma.
• 5–7 years of experience in a GMP environment.
• 3–5 years of experience leading direct reports or teams is preferred.
• Experience with GMPs, FDA and other regulated agency environments is required.
• Experienced in making real time decisions on safety, process, scheduling and personnel‑related issues.
• Ability to prioritize and manage multiple resources in a production environment with flexibility to meet organizational needs.
• Proven leadership, persuasiveness, initiative, and problem solving skills.
• Shift model is 2-3-2 12‑hour shifts starting early Jan 2026.

Responsibilities

• Lead and supervise an aseptic and medical device manufacturing team across multiple shifts.
• Ensure safety and regulatory compliance for all manufacturing activities.
• Coordinate production plans, scheduling, and staff performance against goals.
• Provide coaching, training, and performance evaluations.
• Identify and mitigate operational risks, drive continuous improvement initiatives.
• Prepare and review investigations, deviations and CAPAs with QA and regulatory teams.

Skills

People leadership

Team supervision

GMP compliance

Regulatory knowledge

Problem solving

Education

High School Diploma

Job description

PCI Pharma Services seeks a Manufacturing Supervisor to lead an aseptic and medical device manufacturing team in Bedford, NH. The role requires hands-on leadership across GMP operations, ensuring safety, quality, and efficient production on a 2-3-2, 12-hour shift schedule beginning January 2026.

You will drive staffing, coach performance, and collaborate with QA, Regulatory, and cross‑functional groups to meet capacity and quality targets while mitigating risks and implementing improvements.