Supervisor, Formulation Manufacturing

Thermo Fisher Scientific•Cincinnati, OH

1d•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. 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. Job Description: Join our manufacturing team as a Formulation Manufacturing Supervisor, where you'll manage teams in producing pharmaceutical products. You'll maintain operational excellence while ensuring compliance with cGMP standards and FDA regulations. This role combines technical expertise with people leadership to deliver high-quality products that improve healthcare outcomes. You'll coordinate production schedules, oversee manufacturing processes, and support continuous improvement initiatives. Your leadership will be essential in maintaining quality standards, developing team members, and fostering a culture of safety and innovation. Location/Division Specific Information: Leading a manufacturing operation team to deliver on our safety, quality, delivery, and efficiency objectives related to the manufacturing of oral solid dosage pharmaceutical drugs. Discover Impactful Work: Patheon, by Thermo Fisher Scientific, is redefining the way pharmaceuticals are made with a simplified, end-to-end supply chain for pharmaceutical and biopharmaceutical companies of all sizes. Drug substances and drug products. Development and manufacturing. Small and large molecules. Sterile, oral solid and softgel dosage forms. Patheon offers a comprehensive range of services spanning all phases and scales that is wider and deeper than any other CDMO. Gain instant access to a fully integrated global facilities network. More than 8,000 scientific and professional staff. Over 40 years of experience and innovation!

Requirements

High School Diploma or GED required
5+ years of relevant manufacturing experience
5 years leadership experience
Strong communication skills (written and oral)
Knowledge of cGMP regulations and FDA requirements
Facilitation and presentation skills
Leadership: accountability & execution
Enable strategic focus by prioritizing work and resources across the team to maximize impact
Remove barriers to success and enable a work environment where colleagues can be their best self and are motivated to excel
Analytical Ability; utilize data to define and solve problems
Must be legally authorized to work in the United States now or in the future without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.

Nice To Haves

Bachelor’s Degree preferred in Science, Engineering, Chemistry, or related STEM field
Pharmaceutical experience is a plus
Progression/expansion of roles with an organization

Responsibilities

Manage teams in producing pharmaceutical products.
Maintain operational excellence while ensuring compliance with cGMP standards and FDA regulations.
Coordinate production schedules.
Oversee manufacturing processes.
Support continuous improvement initiatives.
Maintain quality standards.
Develop team members.
Foster a culture of safety and innovation.
Lead all aspects of production schedule while increasing production capacity through de-bottlenecking processes and optimizing systems.
Manage a team of 4-6 supervisors and 50+ manufacturing technicians while handling day-to-day operations and ensuring departmental commitments and results are achieved to meet company objectives.
Establish departmental and individual expectations; mentor direct reports in the performance of their duties; complete performance reviews and provide feedback to team.
Encourage and implement a culture of compliance regarding Safety, EH&S, Quality standards as required by cGMPs, government agencies, and company standards / policies.
Support all site audits and inspections.
Ensure adequate resources are dedicated to correcting important or critical issues via personal involvement, delegated resources, and/or appropriate escalation. This often involves collaborative interaction with other departments.