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4.0 - 8.0 years
0 Lacs
raipur
On-site
As a part of Jaidev Pharma Placement, your role involves having a good knowledge for the execution, documentation, and review of cleaning validation activities in compliance with cGMP, regulatory guidelines, and internal policies. You will be responsible for ensuring that equipment cleaning processes prevent cross-contamination and meet stringent regulatory standards. Your responsibilities will include: - Planning, executing, and documenting cleaning validation and verification protocols (IQ, OQ, PQ). - Coordinating with Production, Quality Control, and Engineering teams for sampling, testing, and equipment readiness. - Developing and reviewing cleaning validation protocols, reports, SOPs, a...
Posted 1 month ago
5.0 - 8.0 years
5 - 8 Lacs
vadodara, gujarat, india
On-site
Design and execute validation protocols for process and cleaning validation activities, including IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), and CV (Cleaning Validation). Develop and maintain a validation master plan (VMP) that aligns with regulatory requirements and organizational goals. Conduct process validation studies to ensure manufacturing processes consistently produce products that meet predefined quality attributes. Analyze process performance and critical parameters during validation runs and document results. Ensure adherence to Good Manufacturing Practices (GMP) during all validation activities. Develop and execute cleaning v...
Posted 3 months ago
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