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 apply, please visit https://www.gmprecruit.com/ and search for Job Reference #: 24330.
To find out more about this opportunity, please contact Patricia Lin @ [email protected]
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Patricia Lin | Registration No: R22105276
