Jobs

    Quality Validation Specialist - Singapore - GMP Technologies

    GMP Technologies
    GMP Technologies Singapore

    1 week ago

    Default job background
    Full time Upper Management / Consulting
    Description

    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: R



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