Job Description
Salary up to 7.80 LPA based on current salary and exprience.
Candidate must have experience from Pharmaceutical Industry and should be ready for traveling for site work across Gujarat and India also.
Description:
Execute CSV activities as per GAMP 5, 21 CFR Part 11, and EU Annex 11
Prepare and execute validation deliverables:
- Validation Plan / VMP sections
- URS, FS, DS
- Risk Assessments (FMEA / Risk-based)
- IQ, OQ, PQ protocols and reports
Validate systems such as PLC, Lab Computerized Systems, LIMS, QMS, DMS, ERP, SAP, Saa S and custom applications
Execute test scripts, collect evidence, and maintain traceability
Work on multiple client projects simultaneously and meet delivery timelines
Support internal, client, and regulatory audits (USFDA, EMA, MHRA, WHO, PIC/s
Participate in client meetings and audit discussions, including global time zones if required
Salary up to 7.80 LPA based on current salary and exprience.
Call now
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Candidate must have experience from Pharmaceutical Industry and should be ready for traveling for site work across Gujarat and India also.
Description:
Execute CSV activities as per GAMP 5, 21 CFR Part 11, and EU Annex 11
Prepare and execute validation deliverables:
- Validation Plan / VMP sections
- URS, FS, DS
- Risk Assessments (FMEA / Risk-based)
- IQ, OQ, PQ protocols and reports
Validate systems such as PLC, Lab Computerized Systems, LIMS, QMS, DMS, ERP, SAP, Saa S and custom applications
Execute test scripts, collect evidence, and maintain traceability
Work on multiple client projects simultaneously and meet delivery timelines
Support internal, client, and regulatory audits (USFDA, EMA, MHRA, WHO, PIC/s
Participate in client meetings and audit discussions, including global time zones if required
Salary up to 7.80 LPA based on current salary and exprience.
Call now
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