Job title: Quality Assurance Associate
Job type: Contract
Emp type: Full-time
Job published: 26-06-2024
Job ID: 32862

Job Description

Our client is one of the world’s leading independent biotechnology companies situated in Singapore. For over 4 decades, they have pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Our client is a pioneer in innovative and inspirational leadership in their social architecture. Join the team for a 6 months contract.

Would this be the next career for you?


Responsible for providing oversight for Quality on-the-floor and operations support, the Associate QA will support manufacturing operations and IPC testing through purposeful presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations. Required to perform 12-hour shift (rotational night and day, or full night shift as required due to business needs). 

Responsibilities include:

  • Support the maturation and continuous improvement of company’s quality systems, including On-the-floor quality oversight, deviation management, change control and ensure that the systems are managed in compliance with cGMP expectations
  • Participate in on the floor triage and support root cause investigations for major investigation if applicable
  • Review and approve minor deviation, change controls, and other quality records such as electronic batch records, SOPs, logbooks and work orders
  • Support in regulatory inspections, and interact directly with regulatory inspectors 
  • Supporting other QA initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation 
  • Escalate any significant event to Quality management in a timely manner.

If you are someone with the following, let’s chat!

  • Comfortable with 12 hours rotational shift (Day/Night and Weekends/PH).
  • At least 1+ years of Quality Assurance experience,
  • Preferably in Pharmaceutical/Manufacturing/Biotechnology industry.
  • Should have knowledge and understanding of GMP pharmaceutical production, pharmaceutical plant operation and associated testing methods.
  • Keen and detailed learner.

Additional Information:

  • Mondays to Sundays | As per business shift schedule
  • Day Shift: 08:00hrs – 20:00hrs (inclusive of 1-hour lunch break)
  • Night Shift: 20:00hrs – 08:00hrs (inclusive of 1-hour lunch break)

Next Steps

Apply today or contact us to discuss this exciting opportunity.
Do note that we will only be in touch if your application is shortlisted.

Re Source Partners Pte Ltd | 202021170E | 20C0279

Kavitha Selvadurai R22110039

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