Manager C&Q – Manufacturing Support
On-site · Hyderabad, Telangana, India
Job Summary
Senior Manager C&Q supports commissioning/qualification lifecycle documentation for engineering projects and GMP systems; collaborates with Engineering, Validation, Quality, Manufacturing, Facilities, Automation, and Project teams to develop inspection-ready C&Q documentation, protocols, reports, and risk assessments; maintains document control and supports audits, with emphasis on compliance, traceability, and continuous improvement in documentation quality across Drug Substance/Drug Product/Finished Product/Packaging or Facilities & Utilities.
Required Qualifications
- Experience in GMP commissioning, qualification, validation, or technical operations
- Experience authoring C&Q lifecycle documentation including qualification protocols and reports
- Knowledge of GMP documentation practices and data integrity requirements
- Strong written and verbal communication skills
- Strong organizational skills and attention to detail
- Experience working in cross-functional project teams
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