Job Description
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 for other exciting opportunities.
Job Tags
Permanent employment, Shift work, Night shift, Rotating shift, Day shift,