Operations Supervisor

About the role

• Work Schedule
• Standard (Mon-Fri)
• Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

About the role

Company information

As part of the ThermoFisher Scientific team, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer! We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Business information

As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus. The Drug Product Division - North America (DPD-NA) is one of the five divisions that make up the Pharma Services Group. We are made up of approximately 4400 colleagues across six sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization.

Position Summary

As an Operations Supervisor, 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’ll coordinate daily operations, mentor and develop team members, and help ensure that every batch meets safety and quality expectations.

Location: Greenville, NC

Hours: Night and Day positions available

Key Responsibilities

• 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, documentation, and adherence to all cGMP, SOP, and regulatory requirements.
• Ensure data integrity and compliance across all operational processes.
• Support deviation investigations, root cause analysis, and corrective actions.
• Promote a culture of safety, inclusion, and continuous improvement through active engagement and example.
• Track and report key production metrics, finding opportunities for efficiency and improvement.
• Maintain a clean, safe, and compliant workspace aligned with EHS and regulatory requirements.
• Communicate effectively between operators, line leads, and supervisors to ensure smooth operations.
• Support the Manager as a delegate during absences and assist with onboarding and training of new employees.

Qualifications

• *Must be Legally authorized to work in the United States without sponsorship.
• *Must be able to pass a comprehensive background check to include drug screening.

Education

• Bachelor’s degree in a STEM or business-related discipline preferred. Equivalent combinations of education, training, and proven experience will be considered.

Experience

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

• Deep understanding of cGMP, aseptic technique, and regulatory compliance.
• Strong interpersonal and communication skills with the ability to inspire and engage others.
• Organized and adaptable, skilled at balancing various priorities in a fast-paced setting.
• Analytical thinker with problem-solving skills and attention to detail.
• Proficiency in Microsoft Office applications (Excel, Word, PowerPoint).
• Commitment to teamwork, accountability, and Thermo Fisher’s 4i Values: Integrity, Intensity, Innovation, and Involvement.

Physical Requirements

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights 20-50 pounds, occasionally pushing and pulling over 100 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

• Occasional weekend shifts required.
• The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job. They are not a comprehensive list of all the duties and responsibilities associated with it.

Competitive wages & Excellent benefits package

• Review our company’s Total Rewards
• Medical, Dental, & Vision benefits-effective Day 1
• Paid Time Off & Holidays
• 401K Company Match up to 6%(after 1 year)
• Tuition Reimbursement – eligible after 90 days
• Employee Referral Bonus
• Employee Discount Program
• Recognition Program
• Charitable Gift Matching
• Company Paid Parental Leave
• We will provide the vital equipment for your role including: computer, monitor, keyboard, mouse, etc.
• We also provide any Personal Protective Equipment you may need including: lab coats, safety glasses, safety shoes, etc.
• Excellent interpersonal skills and ability to work cross-functionally