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ipqa lead (in-process qa lead).

job details

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    job details

    We are looking for a IPQA Lead (In-Process QA Lead) & Senior IPQA Executive to join our MNC Pharmaceutical client.

    You will need to:

    • Monitor Line clearance, Document review, sampling and SFG release activity
    • Review and approval of GMP documents like, QRA, investigations reports, Qualification documents etc. Ensure all time inspection readiness on shop floor
    • Ensure QA oversight on warehouse and Engineering activities. Support Complaints, Deviation and OOS investigation w.r.t. shop floor investigation.
    • Support in execution of the validation protocol, Review and Approval of process validation protocol/ report and continued process verification protocol/ report.
    • Ensure timely closure of CAPAs. Participate in inter departmental meeting & discussions. Co-ordination with other departments for day-to-day activities.

    Requirements:

    • Bachelor’s Degree/Master in any Science (Chemistry/Pharma/Biotechnology) or equivalent
    • More than 5-10 years pharmaceutical industry working experience.
    • Must have experiences in handling IPQA/IPQC

    How to apply?

    To apply online, please click on the appropriate link. Alternatively, please send your resume to shelly.yong@randstad.com.my or Whatsapp only to +6016-663 9410 with provided your latest CV.

    We are looking for a IPQA Lead (In-Process QA Lead) & Senior IPQA Executive to join our MNC Pharmaceutical client.

    You will need to:

    • Monitor Line clearance, Document review, sampling and SFG release activity
    • Review and approval of GMP documents like, QRA, investigations reports, Qualification documents etc. Ensure all time inspection readiness on shop floor
    • Ensure QA oversight on warehouse and Engineering activities. Support Complaints, Deviation and OOS investigation w.r.t. shop floor investigation.
    • Support in execution of the validation protocol, Review and Approval of process validation protocol/ report and continued process verification protocol/ report.
    • Ensure timely closure of CAPAs. Participate in inter departmental meeting & discussions. Co-ordination with other departments for day-to-day activities.

    Requirements:

    • Bachelor’s Degree/Master in any Science (Chemistry/Pharma/Biotechnology) or equivalent
    • More than 5-10 years pharmaceutical industry working experience.
    • Must have experiences in handling IPQA/IPQC

    How to apply?

    To apply online, please click on the appropriate link. Alternatively, please send your resume to shelly.yong@randstad.com.my or Whatsapp only to +6016-663 9410 with provided your latest CV.