Job Description
Key Requirements:
- 10+ years of automation experience in pharmaceutical/biopharma manufacturing
- Strong hands-on experience with Siemens PCS 7 in GMP environments
- Experience in Drug Product or Packaging operations
- Solid understanding of ISA-88 batch standards
- Experience with GAMP5, 21 CFR Part 11 & validation lifecycle
- Exposure to commissioning, qualification, and system integration
- Strong stakeholder coordination and technical leadership skills
Experience with AVEVA, DeltaV, or OT network architecture will be an added advantage.
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