QA( Validation) 4-6 years

Key Responsibilities:

• Execute and review validation protocols (IQ/OQ/PQ) for equipment, utilities, and systems used in sterile injectable manufacturing.
• Perform process validation, cleaning validation, and hold time studies.
• Prepare, review, and maintain validation-related documents as per cGMP and regulatory requirements.
• Coordinate with cross-functional teams including Production, QC, Engineering, and Regulatory Affairs during validation activities.
• Participate in qualification of HVAC, WFI, PW, compressed air systems, autoclaves, and filling line equipment.
• Support regulatory audits (EU, WHO, etc.) and provide necessary validation documentation.
• Ensure compliance with data integrity and good documentation practices.

Qualifications:

• B.Pharm / M.Pharm / M.Sc in a relevant field.
• 4–6 years of experience in QA Validation within a sterile/injectables manufacturing environment.
• Strong understanding of regulatory guidelines ( MHRA, EU GMP).
• Proficient in documentation, protocol writing, and deviation/investigation handling.
• Good interpersonal and communication skills.

Preferred Skills:

• Experience with aseptic processes and cleanroom validation.
• Familiarity with computerized system validation (CSV).
• Knowledge of risk assessment tools like FMEA.

Employment Type: Full-Time

Work Location: Baddi( Jharmajri)
Salary: 30000 to 45000

To Apply:
Please send your updated CV to rahul@gmh.co.in or WhatsApp 7876456719

Job Types: Full-time, Permanent

Pay: ₹30,000.00 - ₹40,000.00 per month

Benefits:

• Cell phone reimbursement
• Flexible schedule
• Food provided
• Health insurance
• Internet reimbursement
• Leave encashment
• Life insurance
• Paid sick time
• Paid time off
• Provident Fund

Work Location: In person