Posted:8 hours ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Key Responsibilities:

  • Develop and execute

    Validation Master Plans (VMP)

    , protocols (IQ/OQ/PQ), and reports for equipment and processes.
  • Perform

    risk assessments

    and ensure compliance with

    cGMP

    and regulatory guidelines.
  • Coordinate with design, production, and quality teams for validation activities.
  • Maintain accurate documentation and ensure timely completion of validation projects.
  • Troubleshoot validation issues and implement corrective actions.
  • Visit Sanand GIDC plant twice a month for validation activities and ensure compliance with site requirements.

  • Stay updated with industry standards and regulatory changes.

Required Qualifications:

  • Education:

    B.E./B.Tech in Mechanical, Electrical, Instrumentation, or related field.
  • Experience:

    2–5 years in equipment/process validation in pharmaceutical or packaging machinery industry.
  • Knowledge of

    GAMP 5

    ,

    FDA

    , and

    ISO

    guidelines.
  • Strong analytical and documentation skills.

Preferred Skills:

  • Familiarity with

    automation systems

    and

    PLC validation

    .
  • Ability to work independently and manage multiple projects.
  • Good communication and team collaboration skills.

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