Senior Validation Specialist
Full time posted 4 months ago in Manufacturing Shortlist Email JobJob Detail
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Job ID 9403
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Career Level Experienced Non-Manager
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Education Level Bachelor\'s Degree
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Industry Pharmaceutical
Job Description
𝐉𝐨𝐛 𝐃𝐞𝐬𝐜𝐫𝐢𝐩𝐭𝐢𝐨𝐧:
- Review & update of Site Validation Master Plan & Related Annexes.
- Follow up Execution of all validation / Qualification activities:
- Facilities Qualification
- Equipment / Systems / Utilities Qualification (URS/FAT/SAT/DQ/IQ/OQ/PQ)
- Manufacturing process validation
- Holding Time studies (Bulk and cleaning).
- Cleaning Method validation
- Computer system validation
- Transport validation
- Building Qualification
- Follow up Execution of Calibration program and execution of calibration plans including execution of thermal mapping studies
- Review of validation / Qualification reports & Related Annexes.
- Review for all standard operating procedures related to the validation activities.
- Ensures that all activities are done according to Approved Validation Master Plan, relevant Who, cGMP and ISO standards.
𝐉𝐨𝐛 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬:
- Bachelor’s degree in Pharmaceutical Science, Science or Engineering
- From 3 – 5 years of experience in Validation/Production and/or Operational Quality
- To gain knowledge of process measurements and validation readiness
- Good Command of English language
Required skills
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