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Job Type

Full Time

Job Description

Designation: Engineer – Validation

Department - Validation

Education: Diploma or BE in Mechanical,

Experience: 2-3 years in machine manufacturing industries


Key Responsibilities:

  1. Execute validation activities for

    pharmaceutical packaging equipment and production lines.

  2. Interpret and work with

    GA drawings, layouts, pneumatic, and electrical schematics.

  3. Ensure compliance with

    cGMP, GEP, and 21 CFR Part 11 standards.

  4. Prepare and manage validation documents:

    IQ, OQ, DQ, PQ, FS

    , service manuals,

    QA

    checklists.
  5. Coordinate with purchase teams for test and material certification requirements.
  6. Perform interlock checks, logical testing,

    IFAT, and CFAT;

    communicate open points to production.
  7. Verify compliance and prepare reports for dispatch clearance.
  8. Support

    ISO audits

    and maintain required documentation.
  9. Ensure timely completion of validation and documentation as per dispatch and validation plans.
  10. Provide on-site qualification support and assist regional engineers when required.
  11. Communicate effectively with export customers and outsourced vendors to meet project requirements.

Desired Skills:

  1. Strong understanding of compliance and validation processes.
  2. Good communication and documentation skills.
  3. Ability to collaborate across teams and with the pharma/healthcare customers .

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