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Open nowPosted 14 days ago

Production Supervisor - 12 hours Rotating Shift

MyCareersFuture94,028 open roles

Pay
SGD 4,000 – SGD 7,500 a month
Where
West, Singapore
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Your applicationOpen nowProduction Supervisor - 12 hours Rotating ShiftMyCareersFuture · West, Singapore

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The clock on this job

Early applications get read.

7.7% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.6%1 day
  2. 3.3%3 days
  3. 7.7%7 days
  4. 14.0%14 days
  5. 33.7%30 days
This job: posted 14 days ago

The posting

Job 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
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