Manufacturing Supervisor, Drug Product

Thermo Fisher Scientific • Plainville, MA

1d • $83,300 - $124,000

About The Position

As part of Thermo Fisher Scientific, the Manufacturing Supervisor contributes to the company’s mission to help make the world healthier, cleaner, and safer. This role leads teams producing pharmaceutical products and combines technical expertise with people leadership to maintain operational excellence and ensure compliance with cGMP standards and FDA regulations.

The supervisor coordinates production schedules, oversees manufacturing processes, and supports continuous improvement initiatives. The role also maintains quality standards, develops team members, and fosters a culture of safety and innovation. The position is based in Massachusetts and is scheduled for the first shift (days), though the requirements note the ability to work rotating shifts, including nights and weekends as needed.

Requirements

• Advanced degree plus 3 years of experience, or a bachelor's degree plus 5 years of experience, in pharmaceutical or biotechnology manufacturing.
• At least 2 years of supervisory or leadership experience in a GMP environment.
• Strong knowledge of cGMP regulations and FDA requirements.
• Expertise in aseptic processing and cleanroom operations.
• Demonstrated ability to lead and develop teams.
• Experience with batch record review and documentation.
• Strong problem-solving and decision-making capabilities.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office applications and manufacturing systems.
• Ability to work rotating shifts, including nights and weekends as needed.
• Ability to stand for extended periods and lift up to 50 pounds.
• Strong project management and organizational skills.
• Ability to manage multiple priorities effectively.
• Demonstrated experience in operational excellence and quality improvements.
• Knowledge of aseptic techniques and environmental monitoring.
• Excellent interpersonal skills and ability to work cross-functionally.
• Legally authorized to work in the United States now and in the future without sponsorship.
• Must be able to pass a comprehensive background check, including drug screening.

Nice To Haves

• Preferred fields of study include science, engineering, chemistry, or a related STEM field.
• Experience with continuous improvement methodologies such as Lean or Six Sigma.

Responsibilities

• Manage teams producing pharmaceutical products.
• Coordinate production schedules and oversee manufacturing processes.
• Maintain operational excellence and ensure compliance with cGMP standards and FDA regulations.
• Support continuous improvement initiatives and operational and quality improvements.
• Maintain quality standards, develop team members, and foster a culture of safety and innovation.
• Review batch records and documentation.
• Work cross-functionally and manage multiple priorities.

Benefits

• Competitive remuneration and eligibility for a variable annual incentive plan bonus.
• Choice of national medical and dental plans and a national vision plan, including health incentive programs.
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement.
• At least 120 hours of paid time off and 10 paid holidays annually.
• Paid parental leave: 3 weeks for bonding and 8 weeks for caregiver leave.
• Accident and life insurance, and short- and long-term disability in accordance with company policy.
• Competitive 401(k) U.S. retirement savings plan.
• Employee Stock Purchase Plan offering eligible colleagues the opportunity to purchase company stock at a discount.
• Career and development prospects.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager