Job Description
Skills:
Equipment Qualification, Calibration, Equipment Risk Assessment, Area Temprature, HVAC Validation, HVAC Qualification,
Instrumentation and Control Solutions is hiring for CSV Engineer.
Industry : Pharma Industry
Location: Goa
Notice Period : Immediate to 30days
Profile - Engineering CSV (Qualification)
Experience - 5-7 years
Interested Candidates Can Email Their Resume To
[HIDDEN TEXT]
For More Details, Contact Us At
9109102346
Skills Required
Change Control, Cqa, URS, cgmp practices , Document Management, OQ, Risk Assessment, Sops, IQ, equipment qualification , Hazop, Tm
Equipment Qualification, Calibration, Equipment Risk Assessment, Area Temprature, HVAC Validation, HVAC Qualification,
Instrumentation and Control Solutions is hiring for CSV Engineer.
Industry : Pharma Industry
Location: Goa
Notice Period : Immediate to 30days
Profile - Engineering CSV (Qualification)
Experience - 5-7 years
- Preparation execution and Review of Facilities, Utilities, Equipment Commissioning & Qualification documents (including QRM, Change control, URS, DQ, IQ, OQ, PQ, QFR, TM SOPs etc.)
- Preparation execution and Review of computerized system qualification / validation (inclusive of URS, FS, HDDS, VP, IQ, OQ, PQ, VSR, TM etc.)
- Preparation execution and Review of Calibration Criticality Assessment (CAT), Calibration certificates.
- Preparation and Review qualification deviations.
- Preparation execution and Review of Equipment Risk Assessment (Alarm Criticality, Audit Trail Frequency, PM frequency, Overall Equipment RA).
- Review of Technical Data Sheet, Basis of Design (BOD), CQA / CPP Determination sheet, Pre-start Safety Review (PSSR), HAZOP.
- Preparation execution and Review of Area Temperature mapping / temperature distribution studies.
- Support on document preparation and drafting, ensure timely document retrieval from QA as per department requirement.
- Any other job/activity, as assigned by the reporting supervisor / management from time to time.
- Back up support for all GMP manufacturing & GxP activity ensuring all equipment complies with Standard Operating Procedures and Policies.
- Preparation & review of risk Assessment related document activity of engineering department.
- Management of engineering quality management system is in compliant state.
- Support on document preparation and drafting, ensure timely document retrieval from QA as per department requirement.
- Drafting, handling & archival of document related to GAP identified during remediation.
- Document Management.
- To comply with cGMP Practices.
- Ensure Data integrity compliance with respect to laid down procedures and systems.
- Management of calibration planning and timely execution as per calibration scheduler.
- Management and adherence to timely execution and completion of qualification activities within due period.
- Management of qualification planning and management of activity schedule as per planner for equipment s.
- Execution of protocol and review of associated reports to ensure its compliance as per regulatory and site norms.
- HVAC Qualification and Validation.
Interested Candidates Can Email Their Resume To
[HIDDEN TEXT]
For More Details, Contact Us At
9109102346
Skills Required
Change Control, Cqa, URS, cgmp practices , Document Management, OQ, Risk Assessment, Sops, IQ, equipment qualification , Hazop, Tm
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