Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of obsolete documents in functional areas.
Review Batch Manufacturing Records (BMR), Packing Material Records (PMR), and Raw material Records (RMR). Report discrepancies or abnormalities to QA Manager.
Ensure Positive Documentation practices throughout departments and plants, no obsolete document to be retained at any functional departments
Ensure to prepare & maintain QMS for Customer complaints, Change control, deviation, NCPR, incident investigation and internal compliances.
Conduct internal audits and maintain audit summaries and CAPA tracking.
Support external audits (regulatory or customer) and ensure timely compliance.
Support in process validation, cleaning validation, equipment qualification.
Provide support for vendor questionnaires and customer queries and share QA-related documents as needed.
Proper issuance and inventory management of product labels. Ensure label usage, reconciliation, and compliance.
Support implementation of safety protocols across QA functions and plant activities. Ensure QA operations adhere to safety and regulatory standards.
Required Skills:
Communication Skills: Transparent verbal and written communication.
Documentation Skills: Proficient in Positive Documentation Practices (GDP)
GMP Knowledge: Sound understanding of cGMP and regulatory compliance
Computer Skills: Proficient in MS Excel, Word, and PowerPoint.
Required Qualification: - M.Sc - Chemistry
Salary :- Upto 5.50 LPA
If you are interested for this opening please send updated resume on same mail with following details.
Total No. of Years Experience :-
Current CTC :-
Expected CTC :-
Notice Period :-
📌 Qa Officer Vapi (India)
🏢 Quality HR India
📍 India
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