Supervisor, Operations (Nights D and C Shift)

Thermo Fisher Scientific

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.

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