Quality Validation Specialist

3 weeks ago


Singapore GMP Technologies Full time

Quality Validation Specialist (1-year Contract)

Our client is a global pharmaceutical company aim to improve the quality of human life. The company is one of the leading MNCs in developing and manufacturing drugs, vaccines, and consumer healthcare products.

Responsibilities:

  • To review, assess and approve validation documents.
  • To plan, conduct, coordinate and initiate quality related meetings.
  • To participate and conduct investigations related to non-conformance events.
  • To prepare and assist in quality compliance audits.
  • To ensure all validation activities are carried out in accordance with regulatory requirements.

Requirements:

  • Diploma in Chemistry/ Science/ Pharmaceutical with more than 5 years of relevant working experience.
  • Degree in Chemistry/ Science/ Pharmaceutical with internship or 1 years of relevant working experience.
  • Hands-on experience in analytical methods/ systems/ equipment validation/ requalification.
  • Good knowledge of GMP, Pharmacopoeia, and quality related regulatory & analytical lab safety requirements.
  • Practical knowledge of performing analytical lab investigation, change control & CAPA.
  • Good knowledge of analytical lab instruments/ equipment/ methods.
  • Willing to train and guide co-workers.
  • Excellent documentation, interpersonal, communication and problem-solving skills.

To find out more about this opportunity, please contact Patricia Lin @

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Patricia Lin | Registration No: R22105276



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