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Lead Formulation Technician Nights


Job Location:

High Point, NC - USA

Monthly Salary: Not provided by the employer
Posted: 9 August 2026 (30 days ago)
Application Deadline: 6 November 2026
Vacancies: 1 Vacancy

Job Summary

Work Schedule

12 hr shift/nights

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Nights: 7pm-7am - rotating 2-2-3 schedule; w/ 10% added night shift differential

About Thermo Fisher Scientific

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every 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 worlds toughest challenges from protecting the environment and ensuring food safety to helping find cures for cancer.

Location / Division Specific Information

This position is located at the High Point North Carolina manufacturing site and is part of the Post Production Operations team. The site supports pharmaceutical manufacturing and packaging operations in a cGMP-regulated environment delivering high-quality products while maintaining a strong commitment to safety compliance and operational excellence.

How Will You Make an Impact

As a Post Production Lead you will provide day-to-day leadership for production associates by coordinating staffing equipment materials and production schedules to achieve safety quality productivity and delivery objectives. Your leadership will help ensure compliance with cGMP requirements while driving operational excellence and continuous improvement across post-production operations.

A Day in the Life
  • Coordinate daily production activities by assigning associates monitoring production schedules and ensuring inspection and packaging operations meet quality productivity and on-time delivery goals.
  • Review Batch Production Records (BPRs) production documentation SAP transactions and production metrics while investigating deviations documenting events and supporting CAPA activities in TrackWise.
  • Lead shift activities by conducting training monitoring equipment readiness verifying line clearances supporting inventory management and collaborating with Quality Assurance Validation Technical Services and Manufacturing leadership.
Education

High School diploma or GED is required

Experience

Required:

  • Minimum of 4 years of experience in manufacturing production operations pharmaceutical biotechnology or a related industrial environment.
  • Experience leading work assignments coordinating production activities or serving as a team or shift lead.
  • Experience working with production documentation and computerized manufacturing systems.

Preferred:

  • Experience in a cGMP-regulated pharmaceutical or life sciences manufacturing environment.
  • Experience with SAP TrackWise Batch Production Records (BPRs) inventory control and production scheduling.
  • Previous project leadership or team leadership experience.
Knowledge Skills Abilities
  • Strong leadership communication and organizational skills with the ability to coordinate production teams conduct training and effectively communicate across multiple departments.
  • Working knowledge of cGMP requirements manufacturing documentation Batch Production Records SAP production scheduling quality systems and continuous improvement practices.
  • Strong analytical and problem-solving skills with the ability to prioritize work make sound operational decisions manage multiple priorities and maintain a high level of quality and compliance in a fast-paced manufacturing environment.
Physical Requirements / Work Environment
  • Regularly required to stand walk reach and use hands while performing production activities.
  • Frequently required to lift push pull and carry materials weighing up to 50 pounds.
  • Must be able to work in a manufacturing environment with moving mechanical equipment and varying noise levels.
  • Requires close visual acuity and color vision for inspection activities.
  • Must wear required Personal Protective Equipment (PPE) including lab coat or uniform safety glasses gloves safety shoes dust masks and hair/facial hair coverings.
  • Must meet applicable DEA security clearance requirements where required.
What We Offer
Compensation
  • Competitive Pay
  • Performance-Related Bonus (where eligible)
  • Annual Merit Performance-Based Increase
Excellent Benefits
  • Medical Dental and Vision Benefits
  • Paid Time Off (PTO) and Annual Leave
  • Employee Referral Bonus
  • 401(k) Retirement Savings Plan (where applicable)
  • Employee Assistance Program
  • Career Development and Advancement Opportunities
  • Training and Professional Development
  • Inclusive and Collaborative Work Environment


Required Experience:

IC


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