Posted:13 hours ago| Platform: Linkedin logo

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On-site

Job Type

Full Time

Job Description

Qualification

Experience

Expected Joining

Job Responsibilities

  • Hands-on experience with pharma packaging machines: tablet counting, liquid filling, cartoning, labeling, capping, induction sealing, etc.
  • Ability to read GA, layout, pneumatic, and electrical drawings.
  • Basic understanding of cGMP compliance, GEP standards, and 21 CFR Part 11.
  • Skilled in preparing IQ, OQ, DQ, PQ, FS documents, service manuals, and QA checklists.
  • Coordination with purchase for test and MOC certificates.
  • Familiarity with interlocks and logical testing procedures.
  • Conducting IFAT and CFAT, reporting open points to production.
  • Ensuring compliance and documentation for dispatch clearance.
  • Participation in ISO audits and maintaining required reports.
  • Supporting site visits and regional engineers for qualification.
  • Effective communication with export customers and outsourced vendors.

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