- Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
- Ensure all operations comply with GMP guidelines and internal quality standards.
- Conduct internal audits to assess adherence to GMP, standard operating procedures (SOPs), and other regulatory requirements.
- Participate in the review and approval of finished product batch records and assist in product release processes.
- Investigate and manage deviations, CAPAs (Corrective and Preventive Actions), and OOS (Out of Specification) results in a timely manner.
- Support the quality control laboratory in ensuring that all testing is performed in accordance with regulatory guidelines and company procedures.
- Prepare, review, and approve validation documentation such as protocols, reports, and qualification documents (IQ/OQ/PQ) for equipment, systems, and processes.
- Assist in the execution of validation activities for equipment, systems, utilities, and processes to ensure compliance with GMP and other regulatory requirements.
- Maintain accurate records of QA-related activities and generate reports for management review.
Required Skills:
- Must be excellent in written and spoken English; net savvy and adept at computer skills.
- Logical thinking.
- Organizing.
- Valuable in communication.
Required Qualification:
- B. Pharm/M. Pharm
Salary: Upto 4.00 LPA
If you are interested in this opening, please send updated resume on the same mail with the following details:
- Total No. of Years Experience: -
- Current CTC: -
- Expected CTC: -
- Notice Period: -
Key Skills:
- Officer
- GMP
- IPQA
Company Profile
Company is into leading pharmaceutical products manufacturing industry.
📌 IPQA Officer (India)
🏢 Quality HR Services
📍 India
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