Executive- QA (Validation)

Panacea Biotec Limited; Solan; Vor Ort; INR 450.000 - 750.000; Vollzeit

Zusammenfassung

Panacea Biotec Limited, Manufacturing Unit (Pharma) in Baddi, Himachal Pradesh, invites professionals for validation and qualification activities with 4-9 years of experience.

The role covers preparation, review and execution of validation/qualification protocols and reports, URS/IQ/OQ/PQ, cleaning and process validation, equipment ID, calibration, and QA documentation in the QC lab context.

Aufgaben

• Preparation and Review of Validation and Qualification related SOPs.
• Execution and verification of Qualification activities at the departments levels.
• To ensure the preparation and Review of URS/DQ/IQ/OQ/PQ related to all new system and equipment to be installed at the site.
• Preparation and review of Validation and Qualification related Protocols and Reports.
• To investigate, evaluate and conclude the non-conformance / deviation related to validation and qualification.
• To prepare Annual Validation Master Planner and to track and update the same, time to time.
• Issuance and control of Validation and Qualification related documents.
• Preparation, review and execution Cleaning Validation protocol and report.
• Preparation, review and execution Process Validation protocol and report.
• To review the protocols and reports for the Microbiological related testing and Analytical Method validation related activities of QC Laboratory.
• To ensure the allotment of Equipment ID to all new equipment to be installed.
• To ensure the Validation and Calibration Status of the equipment at the Site.
• Preparation of Media Fill Protocols and Reports.
• To participate in Media Fill activities and ensure the review and compliance of the activity as per the Batch Records and Protocols
• To perform any other work as assigned by the Head of department.

Jobbeschreibung

MANUFACTURING UNIT (PHARMA), Baddi, Himachal Pradesh, India

4 - 9 Years

PROBATION

Job Description

• 1. Preparation and Review of Validation and Qualification related SOP’s.
• 2. Execution and verification of Qualification Activity at the departments levels
• 3. To ensure the preparation and Review of URS/DQ/IQ/OQ/PQ related to all new system and equipment to be installed at the site.
• 4. Preparation and review of Validation and Qualification related Protocols and Reports.
• 5. To investigate, evaluate and conclude the non-conformance / deviation related to validation and qualification.
• 6. To prepare Annual Validation Master Planner and to track and update the same, time to time.
• 7. Issuance and control of Validation and Qualification related documents.
• 8. Preparation, review and execution Cleaning Validation protocol and report.
• 9. Preparation, review and execution Process Validation protocol and report.
• 10. To review the protocols and reports for the Microbiological related testing and Analytical Method validation related activities of QC Laboratory.
• 11. To ensure the allotment of Equipment ID to all new equipment to be installed.
• 12. To ensure the Validation and Calibration Status of the equipment at the Site.
• 13. Preparation of Media Fill Protocols and Reports.
• 14. To participate in Media Fill activities and ensure the review and compliance of the activity as per the Batch Records and Protocols
• 15. To perform any other work as assigned by the Head of department.

Job Snapshot

Updated Date

22-10-2026

Job ID

JOB_1430

Sub-Function

ONCOLOGY FORMULATION PLANT

Location

Location MANUFACTURING UNIT (PHARMA), Baddi, Himachal Pradesh, India