Supervisor, Operations; Nights D and C Shift

Location:

Greenville, NC

Division:
Pharmaceutical Services Group

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

• Ability to lift up to 40 lbs. without assistance.
• Standing for the full shift.
• Adherence to 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.).

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.

• 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.

• High School Diploma or GED required.
• Bachelor’s degree in a STEM or business‑related discipline preferred.

• 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.

• 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.

• 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.

• 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.
• Relocation assistance:
  Not provided.