Supervisor, Operations (Nights D and C Shift)
About The Position
As a Supervisor, Operations (Night Shift 2-2-3), 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 will coordinate daily operations, mentor and develop team members, and ensure every batch meets safety, regulatory, and quality expectations. This role is critical in maintaining production excellence while fostering a culture of safety, accountability, and continuous improvement. In this leadership role, you will directly influence the production of sterile pharmaceutical products that support global healthcare needs. By driving operational efficiency, ensuring regulatory compliance, and developing high-performing teams, you will help Thermo Fisher Scientific deliver on its mission to make the world healthier, cleaner, and safer.
Requirements
- High School Diploma or GED required.
- Minimum five (5) years of experience in pharmaceutical, biopharmaceutical, or sterile manufacturing/filling
- At least two (2) years of leadership experience with direct or indirect reports
- Strong understanding of cGMP, aseptic technique, and regulatory compliance
- Strong interpersonal and communication skills with the ability to inspire and engage others
- Organized and adaptable, able to manage multiple priorities in a fast-paced environment
- Analytical problem-solver with attention to detail
- Proficiency in Microsoft Office (Excel, Word, PowerPoint)
- Commitment to teamwork, accountability, and Thermo Fisher’s 4i Values: Integrity, Intensity, Innovation, and Involvement
- Ordinary ambulatory skills and coordination sufficient to move throughout manufacturing and office areas
- Ability to stand, walk, stoop, kneel, and crouch for prolonged periods
- Ability to lift, carry, and move 20–50 pounds; occasionally push/pull over 100 pounds
- Manual dexterity for equipment operation and computer use
- Visual acuity to operate equipment and read documentation
- Ability to sit, reach, talk, and hear for extended periods
- Must be able to pass a comprehensive background check, including a drug screening
- Must be legally authorized to work in the United States without sponsorship
Nice To Haves
- Bachelor’s degree in a STEM or business-related discipline preferred.
- Equivalent combinations of education, training, and demonstrated experience will be considered.
- Hands-on experience in aseptic or sterile product formulation strongly preferred
- Experience using SAP or other manufacturing systems
Responsibilities
- 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 and ensure adherence to all cGMP, SOP, and regulatory requirements
- Support deviation investigations, root cause analysis, and corrective actions
- Promote a culture of safety, inclusion, and continuous improvement
- Track and report key production metrics, identifying opportunities for efficiency and improvement
- Maintain a clean, safe, and compliant workspace aligned with EHS and regulatory requirements
- Communicate effectively across operators, line leads, and management to ensure smooth operations
- Serve as delegate for the Manager during absences and support onboarding and training of new employees
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What This Job Offers
Job Type
Full-time
Career Level
Manager
Education Level
High school or GED
