Supervisor, Operations (Nights D and C Shift)

Work Schedule

Environmental Conditions

Job Description

Supervisor Operations (Night Shift 2-2-3)

Location: Greenville NC
Division: Pharmaceutical Services Group
Shift: 6:00 PM 6:00 AM (2-2-3 rotation)

Division Information Pharmaceutical Services Group (Greenville NC)

The Greenville NC site is a large multipurpose pharmaceutical manufacturing and packaging campus supporting both clinical and commercial production. The facility specializes in solid dose and sterile manufacturing including aseptic filling lyophilization biologics small molecules controlled substances and secondary packaging. With advanced technical capabilities and a strong global regulatory inspection history the site plays a critical role in delivering high-quality pharmaceutical products worldwide.

Work Schedule

12-hour night shift on a 2-2-3 rotation (6:00 PM 6:00 AM)
Occasional weekend shifts required

Environmental Conditions

• Ability to lift up to 40 lbs. without assistance

• Standing for the full shift

• Adherence to all Good Manufacturing Practices (GMP) Safety Standards

• Cleanroom environment: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc. allowed

• Some degree of Personal Protective Equipment (PPE) required (safety glasses gowning gloves lab coat ear plugs etc.)

Job Summary

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.

How You Will Make an Impact

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.

What You Will Do

• 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

How You Will Get Here

Education

• High School Diploma or GED required.

• Bachelors degree in a STEM or business-related discipline preferred.

Equivalent combinations of education training and demonstrated experience will be considered.

Experience

• 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

• Hands-on experience in aseptic or sterile product formulation strongly preferred

• Experience using SAP or other manufacturing systems

Knowledge Skills and Abilities

• 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 Fishers 4i Values: Integrity Intensity Innovation and Involvement

Physical Requirements

• 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 2050 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

Relocation Assistance: Not provided

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

Why Join Us

When you join Thermo Fisher Scientific you become part of a collaborative team that values curiosity integrity and excellence. Youll have access to continuous learning leadership development and opportunities to grow your career while contributing to something bigger than yourself.

At Thermo Fisher youll do work that truly matters helping us deliver on our mission to make the world healthier cleaner and safer.