Officer, QA Validation

Vizen Life Sciences Pvt Ltd; Hyderabad; On-site; INR 300,000 - 520,000; Full time

Job summary

Vizen Life Sciences Pvt Ltd in Hyderabad is seeking a QA/QC Pharmacist to monitor manufacturing areas, ensure GMP compliance, and maintain quality records. The role requires a Bachelor of Pharmacy and strong documentation practices.

You will coordinate qualification/validation activities with cross-functional teams to ensure timely completion. Candidates should have a Bachelor of Pharmacy and be able to review URS, DQ, and supplier documents, while assisting in validation protocol development

Qualifications

• Bachelor of Pharmacy degree required.

Responsibilities

• Routine monitoring of Manufacturing Areas.
• GMP inspection and review of quality records for other departments.
• Monitor and ensure compliance with current GMP requirements.
• Maintain good documentation recording and updating.
• Review URS, DQ and supplier documents related to qualification.
• Prepare Validation / Qualification protocols and reports.
• Execute and review qualification, re-qualification and validation activities for equipment, systems, facilities and plant utilities.
• Ensure adequacy of validations carried out as per prescribed procedures.
• Coordinate with cross-functional teams for qualification/validation activities to meet deadlines.
• Coordinate calibrations before performing qualifications.

Education

Bachelor of Pharmacy

Job description

Responsibilities

• Responsible for routine monitoring of Manufacturing Areas.
• Responsible for the routine GMP Inspection & review of Quality Records of other departments.
• To monitor and ensure compliance level of organization is as per current GMP requirement
• Good Documentation recording and updation.
• Responsible for review of URS, DQ and vendor / suppliers documents related to qualification.
• Responsible for preparation of Validation / Qualification protocol and report.
• Responsible for execution and review of qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant Utilities.
• Responsible for adequacy of execution of validations being carried out at prescribed procedures.
• Responsible For Assurance Of Calibrations Before Performing Qualifications.
• Responsible to co-ordinate with cross functional department personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities.

Qualification & Experience

• B. Pharmacy