About this Production Supervisor role at Thermo Fisher Scientific
Work Schedule
Flex 12 hr shift/daysEnvironmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), WarehouseJob Description
PLEASE NOTE: THIS IS A 12-HOURS ROTATING SHIFT ROLE BASED IN JOO KOON, SINGAPORE
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.
RESPONSIBILITIES:
Manage teams in producing pharmaceutical products.
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.
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.
REQUIREMENTS:
Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in pharmaceutical or biotechnology manufacturing
Preferred Fields of Study: Science, Engineering, Chemistry, or related STEM field
2+ years of supervisory/leadership experience in a GMP environment
Strong knowledge of cGMP regulations and FDA requirements
Expertise in aseptic processing and cleanroom operations
Demonstrated ability to lead and develop teams
Experience with batch record review and documentation
Strong problem-solving and decision-making capabilities
Excellence in written and verbal communication skills
Proficiency with Microsoft Office applications and manufacturing systems
Ability to work rotating shifts, including nights/weekends as needed
Physical ability to stand for extended periods and lift up to 50 pounds
Strong project management and organizational skills
Experience with continuous improvement methodologies (Lean, Six Sigma)
Ability to effectively manage multiple priorities
Demonstrated experience in operational excellence and quality improvements
Knowledge of aseptic techniques and environmental monitoring
Excellent interpersonal skills and ability to work cross-functionally
