3) 15% shift differential

Thermo Fisher Scientific•Greenville, NC

13d•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. 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. As part of the Pharmaceutical Services Group (PSG), the Greenville, North Carolina Steriles site manufactures high-quality sterile pharmaceutical products in a fast-paced, regulated environment supporting customers from development through commercial production. We have industry-leading sterile injectable facilities providing solutions to take essential products from pre-clinical to the market. Pharmaceutical products come in many different dose forms including inhalations, oral dose, cream/ointment and injectables. Discover Impactful Work: The B52 Supervisor (Combi 1) provides frontline leadership for manufacturing and filling operations, ensuring safe, compliant, and efficient production of high-quality pharmaceutical products. In this role, you will lead production teams, drive continuous improvement initiatives, and support operational excellence while maintaining compliance with cGMP and regulatory requirements.

Requirements

5+ years of manufacturing experience.
Minimum 2 years of leadership experience.
Must be legally authorized to work in the United States WITHOUT SPONSORSHIP OF ANY KIND NOW OR IN THE FUTURE.
Must be able to pass a comprehensive background check, which includes a drug screen.

Nice To Haves

Bachelor’s degree in Physical, Biological, Chemical, Production Science, or related field strongly preferred.
Sterile pharmaceutical manufacturing experience preferred.
Knowledge of aseptic processing and manufacturing operations.
Ability to manage multiple priorities in a fast-paced environment.
Strong organizational skills and attention to detail.
Self-motivated, dependable, and results oriented.
Excellent interpersonal, written, and verbal communication skills.
Ability to lead technical teams, resolve complex problems, and motivate employees.
Strong judgment, confidentiality, and time management skills.

Responsibilities

Lead and develop production teams while fostering accountability, engagement, and organizational change.
Ensure production, quality, schedule, and cost objectives are achieved while addressing deviations.
Maintain compliance with cGMPs, FDA, OSHA, and internal quality requirements.
Plan, monitor, and adjust daily production schedules to meet customer commitments.
Promote a strong safety culture and ensure adherence to safety procedures.
Evaluate employee performance, coach team members, and complete performance reviews.
Support technical issue resolution and successful transfer of new manufacturing processes.
Develop and maintain production documentation, procedures, and work instructions.
Drive continuous improvement and cost reduction initiatives.
Monitor attendance, approve timecards, ensure required training completion, and perform other assigned duties.