Singapore | Medical Device | Biotechnology | GMP/GDP Compliance
Join a high-performing team that produces medical and biotechnology components meeting the highest global quality and safety standards. As a Production Operator, you’ll play a vital role in ensuring every product reflects precision, consistency, and compliance.

About the Company

Our client is a global manufacturer specializing in medical device and biotechnology components. With a strong focus on precision manufacturing, quality assurance, and regulatory compliance, they partner with leading healthcare innovators to deliver reliable, life-enhancing products. Through advanced production technologies and a culture of continuous improvement, they maintain excellence in every process—from assembly to final inspection.

About the Role

As a Production Operator, you’ll be responsible for operating and assembling products according to established Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). You’ll collaborate closely with engineers and quality teams to ensure every product meets safety, performance, and regulatory requirements while contributing to continuous improvement initiatives across the production floor.

What’s in It for You

• Work in a GMP-certified cleanroom manufacturing environment.
• Gain exposure to regulated production processes in medical device and biotech manufacturing.
• Learn advanced assembly and inspection techniques.
• Join a supportive team culture focused on safety, quality, and collaboration.
• Access career development opportunities within a stable and growing industry.

Key Responsibilities

• Operate, assemble, and inspect products according to work instructions and quality standards.
• Meet daily production targets while maintaining accuracy, cleanliness, and safety.
• Identify and report issues related to materials, equipment, or processes.
• Maintain documentation accuracy in compliance with GDP guidelines.
• Adhere to GMP protocols and workplace safety requirements.
• Participate in continuous improvement projects and support other assigned production tasks.

Requirements

• NITEC, Higher NITEC, or Diploma in Manufacturing, Engineering, Biotechnology, or a related field.
• 1–3 years of experience in a regulated manufacturing environment preferred.
• Knowledge of GMP and GDP principles.
• Strong attention to detail and quality-focused mindset.
• Willingness to work in a cleanroom and on rotating or fixed shifts, if required.

Additional Details

Eligibility

• Open to Singapore Citizens and Permanent Residents (due to current work pass quota availability).
• Candidates with cleanroom experience are preferred; training can be provided for those with prior exposure.
• Must be comfortable wearing a cleanroom jumpsuit for extended hours (≥9 hours daily).
• Work involves light physical tasks and requires stamina for 12-hour shifts (1-hour break).
• No exposure to toxic chemicals – safe, clean, and fully compliant environment.
  

Working Hours

• Monday–Thursday: 8 AM–8 PM (Day) or 8 PM–8 AM (Night)
• Friday–Sunday: Optional overtime for Singaporeans/PRs
• Rotating shifts preferred; permanent day shift possible
• Transport provided (fixed pick-up and drop-off points)

Compensation & Benefits

• Basic Salary: Up to SGD 1,850
• Hardship Allowance for cleanroom/jumpsuit environment
• Performance Incentive:
• Retention / Stay-On Incentives
• Night Shift Allowance
• Overtime Pay
• Additional Benefits:
  • Annual Wage Supplement (AWS)
  • Performance Bonus
  • Medical & Dental Insurance
  • Yearly salary increments aligned with CPI standards
  • Promotion opportunities based on merit and performance

👉 Interested applicants:
Send your CV to niolar@dartsolutions.sg or upload your profile at Dart Solutions Careers for other exciting opportunities.