Surendra Parampudi

Sr Bench Sales Recruiter - Medical Devices Pharma @RevereIT LLC

I market my consultants Profiles for Quality & Validation Positions in Pharmaceutical/ Medical Devices & Life science industries. I have successfully provided my Best consultants to our Clients.I offer a full range of validation and quality systems services for FDA/ Life Sciences Industries.My areas of specialization are,1. Validation Engineer2. Quality Engineer 3. Process Validation Engineer4. Equipment Validation5. Computer system Validation (CSV)6. Cleaning Validation7. Quality Assurance/Test Engineer8. Packaging Validation Engineer9. V&V Engineer10. R&D Test Engineer11. Regulatory Affairs12. Supplier Quality Engineer13. Compliance Engineer14. Manufacturing Engineer15. CQV Engineer (Commissioning & Qualification)16. Document control specialist17. Quality & Design Engineer18. Manufacturing & Design Engineer19. Complaint Handling/Investigation20. Technical writers ( Pharma/Medical Devices)21. Business Analyst (Pharma /Medical Device) and moreKeywords: Validation Protocols (IQ, OQ, PQ); Validation Master Plans; LIMS; SOP\'s; Process Validation; CAPA; Facility Qualification; Equipment Qualification; Clean in place (CIP), COP; Utility systems validation; Packaging Validation; 21 CFR Part 11; ISO 9001,ISO 13485, cGxP (GMP/GLP/GCP), Gage R&R, Unique Device identification (UDI), Quality system management, Design control, Quality control, Design/ Quality Assurance,DFMEAs, PFMEAs, Traceability Matrix, DFMEAs Risk Management, Quality Analysis; Gap/ Risk assessment; RTM; MDR’s, Clinical Documentation; GDP; CAPA;CAD; Lean SIX SIGMA; Minitab; Trackwise; ARLSg; Auto CAD, Matlab, Trial Master File (TMF), LabWare LIMS; Pharmacovigilance /R&D/Manufacturing; GXP Regulations; EDI; HIPAA; HL7, Quality System Regulations (QSR), compliance and ISO standards, FDA, CE marking, and ICH guidelines, and regulations.