Hiring.Camp

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

Thermofisher

·

Jan 22, 2026

Location
US - Greenville, NC - 5900 Martin Luther King Jr. Highway, United States of America
Workplace
Onsite
Type
Full-time
Department
Operations
Visa
Not sponsored
Source
Workday

Description

Work Schedule

12 hr shift/days

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

Job Description

Job Title: Supervisor, Formulation Manufacturing (Day Shift 2-2-3)

Location/Division Specific Information

Pharmaceutical Services Group – Greenville, NC

Hours: 6AM - 6PM (2/2/3 rotation)

  • Relocation assistance is NOT provided
  • Must be legally authorized to work in the United States without sponsorship.
  • Must be able to pass a comprehensive background check, which includes a drug screening.

How You Will Make an Impact

As a Team Leader in Formulation Manufacturing, 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.

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, 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.

How You Will Get Here

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, and 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.

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 — and help us deliver on our mission to make the world healthier, cleaner, and safer.

If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here for further assistance.  ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Skills

ExcelSAPGMPCompliance

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