Thermo Fisher Scientific · Bengaluru
Manufacturing & Operations
Thermo Fisher Scientific is hiring a Supervisor, Operations - 12 Hour Nights (2/2/3) 15% shift differential in Bengaluru, Karnataka. Posted 11 September 2026. Apply directly on Thermo Fisher Scientific's own careers site — no account needed.
Work Schedule
12 hr shift/nightsEnvironmental Conditions
Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowedJob Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. 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.
As part of the Pharmaceutical Services Group (PSG), the Greenville, North Carolina Steriles site manufactures high-quality sterile pharmaceutical products in a fast-paced, regulated environment supporting customers from development through commercial production.
Excellent Benefits Package
Review our company’s Total Rewards
Medical, Dental, & Vision benefits-effective Day 1
Paid Time Off & Holidays
401K Company Match up to 5%
Tuition Reimbursement – eligible after 90 days!
Employee Referral Bonus
Employee Discount Program
Recognition Program
Charitable Gift Matching
Company Paid Parental Leave
Career Advancement Opportunities
Location/Division Specific Information
Greenville, NC
Hours: 6pm-7am (2-2-3 schedule) 15% shift differential
RELOCATION ASSISTANCE IS NOT PROVIDED
We have industry-leading sterile injectable facilities providing solutions to take essential products from pre-clinical to the market. Pharmaceutical products come in many different dose forms including inhalations, oral dose, cream/ointment and injectables.
The B52 Supervisor (Combi 1) provides frontline leadership for manufacturing and filling operations, ensuring safe, compliant, and efficient production of high-quality pharmaceutical products. In this role, you will lead production teams, drive continuous improvement initiatives, and support operational excellence while maintaining compliance with cGMP and regulatory requirements.
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