Supervisor, Operations (Nights D and C Shift)

Work Schedule

12 hr shift/nights

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Warehouse

Job Description

Supervisor, Operations (Night Shift 2-2-3)

Location: Greenville, NC
Division: Pharmaceutical Services Group
Shift: 6:00 PM – 6:00 AM (2-2-3 rotation)

Division Information – Pharmaceutical Services Group (Greenville, NC)

The Greenville, NC site is a large, multipurpose pharmaceutical manufacturing and packaging campus supporting both clinical and commercial production. The facility specializes in solid dose and sterile manufacturing, including aseptic filling, lyophilization, biologics, small molecules, controlled substances, and secondary packaging. With advanced technical capabilities and a strong global regulatory inspection history, the site plays a critical role in delivering high-quality pharmaceutical products worldwide.

Work Schedule

12-hour night shift on a 2-2-3 rotation (6:00 PM – 6:00 AM)
Occasional weekend shifts required

Environmental Conditions

• Ability to lift up to 40 lbs. without assistance

• Standing for the full shift

• Adherence to all Good Manufacturing Practices (GMP) Safety Standards

• Cleanroom environment: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair, etc. allowed

• Some degree of Personal Protective Equipment (PPE) required (safety glasses, gowning, gloves, lab coat, ear plugs, etc.)

Job Summary

As a Supervisor, Operations (Night Shift 2-2-3), you will lead a skilled team of manufacturing technicians dedicated to producing sterile pharmaceutical products that meet the highest standards of quality and compliance. You will coordinate daily operations, mentor and develop team members, and ensure every batch meets safety, regulatory, and quality expectations.

This role is critical in maintaining production excellence while fostering a culture of safety, accountability, and continuous improvement.

How You Will Make an Impact

In this leadership role, you will directly influence the production of sterile pharmaceutical products that support global healthcare needs. By driving operational efficiency, ensuring regulatory compliance, and developing high-performing teams, you will help Thermo Fisher Scientific deliver on its mission to make the world healthier, cleaner, and safer.

What You Will Do

• Lead and develop a team of manufacturing operators to achieve production, safety, and quality goals

• Plan daily work, assign resources, and supervise progress to ensure schedule adherence

• Ensure compliance with cGMP, SOPs, and data integrity standards through accurate documentation and process execution

• Partner with Quality, Engineering, and Maintenance to resolve process and equipment issues

• Oversee batch record accuracy and ensure adherence to all cGMP, SOP, and regulatory requirements

• Support deviation investigations, root cause analysis, and corrective actions

• Promote a culture of safety, inclusion, and continuous improvement

• Track and report key production metrics, identifying opportunities for efficiency and improvement

• Maintain a clean, safe, and compliant workspace aligned with EHS and regulatory requirements

• Communicate effectively across operators, line leads, and management to ensure smooth operations

• Serve as delegate for the Manager during absences and support onboarding and training of new employees

How You Will Get Here

Education

• High School Diploma or GED required.

• Bachelor’s degree in a STEM or business-related discipline preferred.

Equivalent combinations of education, training, and demonstrated experience will be considered.

Experience

• Minimum five (5) years of experience in pharmaceutical, biopharmaceutical, or sterile manufacturing/filling

• At least two (2) years of leadership experience with direct or indirect reports

• Hands-on experience in aseptic or sterile product formulation strongly preferred

• Experience using SAP or other manufacturing systems

Knowledge, Skills, and Abilities

• Strong understanding of cGMP, aseptic technique, and regulatory compliance

• Strong interpersonal and communication skills with the ability to inspire and engage others

• Organized and adaptable, able to manage multiple priorities in a fast-paced environment

• Analytical problem-solver with attention to detail

• Proficiency in Microsoft Office (Excel, Word, PowerPoint)

• Commitment to teamwork, accountability, and Thermo Fisher’s 4i Values: Integrity, Intensity, Innovation, and Involvement

Physical Requirements

• Ordinary ambulatory skills and coordination sufficient to move throughout manufacturing and office areas

• Ability to stand, walk, stoop, kneel, and crouch for prolonged periods

• Ability to lift, carry, and move 20–50 pounds; occasionally push/pull over 100 pounds

• Manual dexterity for equipment operation and computer use

• Visual acuity to operate equipment and read documentation

• Ability to sit, reach, talk, and hear for extended periods

Relocation Assistance: Not provided

Must be able to pass a comprehensive background check, including a drug screening

Must be legally authorized to work in the United States without sponsorship

Why Join Us

When you join Thermo Fisher Scientific, you become part of a collaborative team that values curiosity, integrity, and excellence. You’ll have access to continuous learning, leadership development, and opportunities to grow your career while contributing to something bigger than yourself.

At Thermo Fisher, you’ll do work that truly matters — helping us deliver on our mission to make the world healthier, cleaner, and safer.