Posted:23 hours ago| Platform:
On-site
Full Time
JOB TITLE : Sr. QA Officer Requirements: 1. B.Pharm/M.Pharm with 4–5 years QA experience in oral solid dosage form (tablet, capsule and Dry Syrup 2. Strong documentation, audit preparedness, and regulatory understanding Key Responsibilities: 1. Manage QMS: Deviation, Change Control, CAPA, Risk Assessment, Product Complaints, Recall 2. Review & Maintain: - BMR, BPR, MFR, MPR, COA - SOPs, STPs, Specifications, Logbooks - APQR, Stability & Validation Protocols 3. Execute/Support: - Process & Cleaning Validation, Hold Time Studies, Line Clearance, In-process Checks - Internal Audits, Self-inspections, GMP Training - Vendor Qualification & Technology Transfer Documents - Ensure compliance with GMP & WHO-guidelines If interested, reach out at chhavi@mediwell.in Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹30,000.00 per month Schedule: Day shift Supplemental Pay: Overtime pay Performance bonus Shift allowance Application Question(s): Do you have at least 4 years of hands-on experience in QA for oral solid dosage forms (tablets/capsules/dry syrup)? Can you list the types of QMS documentation (e.g., deviation, CAPA, change control, APQR) you have handled independently? Have you been involved in process validation, cleaning validation, or regulatory audits? If yes, please describe your role and responsibilities. Experience: QA : 2 years (Required) Work Location: In person Speak with the employer +91 9216044412
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