Supervisor, Formulation Manufacturing (Thursday- Saturday Nights)

Thermo Fisher Scientific•Cincinnati, OH

About The Position

As part of Thermo Fisher Scientific, the Formulation Manufacturing Supervisor helps produce pharmaceutical products and supports the company’s mission to improve health, safety, and the environment. The role manages manufacturing teams, maintains operational excellence, and ensures compliance with cGMP standards and FDA regulations. Responsibilities include coordinating production schedules, overseeing manufacturing processes, supporting continuous improvement, maintaining quality standards, developing team members, and fostering a culture of safety and innovation. The schedule is Thursday through Saturday, 6:00 p.m. to 6:30 a.m., with a 15% shift differential. The work involves cleanroom and GMP conditions, production equipment, PPE, and hazardous or toxic materials. Relocation assistance is not available. Applicants must be legally authorized to work in the United States without current or future employer-sponsored work authorization. Employment is contingent on applicable pre-employment screening, including a background check and drug screening.

Requirements

Advanced degree plus 3 years of experience, or a bachelor's degree plus 5 years of experience in pharmaceutical or biotechnology manufacturing.
At least 2 years of supervisory or leadership experience in a GMP environment.
Strong knowledge of cGMP regulations and FDA requirements.
Expertise in aseptic processing and cleanroom operations.
Demonstrated ability to lead and develop teams.
Experience with batch record review and documentation.
Strong problem-solving and decision-making capabilities.
Excellent written and verbal communication skills.
Proficiency with Microsoft Office applications and manufacturing systems.
Ability to work rotating shifts, including nights and weekends as needed.
Ability to stand for extended periods and lift up to 50 pounds.
Strong project management and organizational skills.
Ability to manage multiple priorities effectively.
Demonstrated experience in operational excellence and quality improvements.
Knowledge of aseptic techniques and environmental monitoring.
Excellent interpersonal skills and ability to work cross-functionally.
Legally authorized to work in the United States without current or future employer-sponsored work authorization.
Successful completion of applicable pre-employment requirements, including a background check and drug screening.

Nice To Haves

Preferred fields of study: Science, Engineering, Chemistry, or a related STEM field.
Experience with continuous improvement methodologies such as Lean or Six Sigma.

Responsibilities

Manage teams producing pharmaceutical products.
Maintain operational excellence and ensure compliance with cGMP standards and FDA regulations.
Coordinate production schedules and oversee manufacturing processes.
Support continuous improvement initiatives.
Maintain quality standards and foster a culture of safety and innovation.
Develop team members.