Hiring - Sr. Executive – Equipment Validation & Qualification - Pharma Industry

Sr. Executive – Equipment Validation & Qualification

4 Nos.
133625
Full Time
6.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Site Engg/Service/Project Mgt/After sales
Pharma/Biotech/Clinical Research
Job Description:
  • Work Location: Pithampur
  • Days of working - 6 days
  • Shift timings - 9 hrs duty
  • Salary - Best in the market
  • Benefits - Pf , Mediclaim , Insurance 
  • Gender: Male
    Payroll - Talisman HR Solutions

Role Purpose

Responsible for planning and execution of equipment qualification and validation activities (DQ, IQ, OQ, PQ) for manufacturing and utility systems in compliance with GMP and regulatory requirements.

Key Responsibilities

Validation & Qualification Execution

  • Prepare and execute DQ, IQ, OQ, PQ protocols and reports.
  • Ensure qualification of manufacturing equipment and utilities.
  • Coordinate risk assessments (FMEA / impact assessment).
  • Support validation master plan (VMP) preparation and updates.

Equipment & Utility Coverage

Experience in qualification of:

  • Reactors, distillation columns, centrifuges, dryers
  • Tanks, heat exchangers, pumps
  • Process piping systems
  • Utilities: HVAC, purified water (PW), WFI, clean steam, compressed air, nitrogen, vacuum systems

Documentation & Compliance

  • Ensure compliance with GMP, 21 CFR Part 11 (where applicable), and regulatory guidelines.
  • Maintain validation documentation as per audit requirements.
  • Handle change control, deviation and CAPA related to validation activities.
  • Support regulatory audits and inspections.

Cross-Functional Coordination

  • Coordinate with Engineering, Production, QA, QC and Automation teams.
  • Review P&IDs, layouts and URS documents.
  • Support FAT, SAT and commissioning activities from validation perspective.

Qualifications & Experience

  • B.E./B.Tech in Chemical / Mechanical OR M.Pharm / B.Pharm
  • 5–8 years of experience in Pharma / API manufacturing
  • Strong experience in equipment and utility qualification

Key Skills

  • Strong knowledge of GMP and validation lifecycle
  • Documentation and protocol writing expertise
  • Good understanding of process equipment and utilities
  • Audit readiness and regulatory exposure

 Name - Willita Prashant Ved 
Mail ID -  Share your CV at: sourcing@talismanstaffing.com
Contact Number - 77100 64829

Company Profile

MNC ---ceutical industry, the discovery, development, and manufacture of drugs and medications

 

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  • Recruiters will evaluate your candidature and will get in touch with you.

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