Job Overview
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Date PostedMarch 19, 2024
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Location (State / UT)
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Expiration dateMarch 14, 2025
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Experience6 Years, 9 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
Roles and Responsibilities:
- In-process Quality Assurance during production activity including line clearance and sampling
at different stages of Processing /Packing as per the requirement – MDI/DPI/DERMA - Review of Master Documents such as BMR/BPR, Test batch monitoring protocols/process
validation protocol and reports, and equipment qualification documents. - Swab/Rinse sample collection of production equipment.
- Review of executed BMR/ BPR/ Logbooks, and investigation reports. Preparation of trends
Deviation, IP-OOS, Change Control, Market Complaint, CAPA. - Review of executed batch records, and preparation of QA SOPs.
- Visual Examination of FP control sample, preparation of hold time study protocol.
- Review of equipment CSV documents.
Qualification: B. Pharma, MS, M.Sc
Experience: 6-9 Years
Women Candidates are Preferred