Validation Executive

Drlogy

India

On-site

INR 400,000 - 700,000

Full time

14 days+
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Job summary

Drlogy is seeking an experienced Validation Executive to oversee equipment, process, cleaning, and utility validation activities within pharmaceutical manufacturing environments. The ideal candidate will be skilled in validation documentation and protocol execution, ensuring compliance with GMP and regulatory requirements.

This role involves coordinating qualification activities, monitoring validation schedules, and participating in audits to uphold pharmaceutical quality standards.

Qualifications

  • Experienced in executing validation activities in pharmaceutical environments.
  • Skilled in ensuring compliance with regulatory requirements.
  • Adept in maintaining documentation systems related to validation.

Responsibilities

  • Execute process, equipment, and cleaning validation activities efficiently.
  • Prepare validation protocols, reports, and documentation accurately.
  • Ensure compliance with GMP and pharmaceutical validation standards.
  • Coordinate qualification and calibration activities effectively.
  • Support utility and HVAC validation operations.
  • Review validation records and maintain documentation systems.
  • Investigate validation deviations and support corrective actions.

Skills

Validation documentation
GMP compliance
Protocol execution
Equipment qualification

Job description

Experienced Validation Executive responsible for executing equipment, process, cleaning, and utility validation activities within pharmaceutical manufacturing environments. Skilled in validation documentation, protocol execution, qualification activities, and GMP compliance. Adept at ensuring validation compliance with pharmaceutical quality standards and regulatory requirements.

Responsibilities
  • Execute process, equipment, and cleaning validation activities efficiently.
  • Prepare validation protocols, reports, and documentation accurately.
  • Ensure compliance with GMP and pharmaceutical validation standards.
  • Coordinate qualification and calibration activities effectively.
  • Support utility and HVAC validation operations.
  • Review validation records and maintain documentation systems.
  • Investigate validation deviations and support corrective actions.
  • Coordinate with QA, production, and engineering teams.
  • Participate in audits and regulatory inspection activities.
  • Monitor validation schedules and ensure timely completion.
  • Ensure adherence to SOPs and quality procedures consistently.
  • Maintain records related to equipment and utility qualification.
  • Support risk assessment and process improvement initiatives.
  • Assist in training staff on validation and compliance practices.
  • Ensure operational readiness and compliance with safety standards.
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