Experience

RevereIT LLC

• United States
• Staffing and Recruiting
• 1 - 100 Employee

• Sr Bench Sales Recruiter - Medical Devices | Pharma

  • Jun 2022 - Present

  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 Engineer 2. Quality Engineer 3. Process Validation Engineer 4. Equipment Validation 5. Computer system Validation (CSV) 6. Cleaning Validation 7. Quality Assurance/Test Engineer 8. Packaging Validation Engineer 9. V & V Engineer 10. R&D Test Engineer 11. Regulatory Affairs 12. Supplier Quality Engineer 13. Compliance Engineer 14. Manufacturing Engineer 15. CQV Engineer (Commissioning & Qualification) 16. Document control specialist 17. Quality & Design Engineer 18. Manufacturing & Design Engineer 19. Complaint Handling/Investigation 20. Technical writers ( Pharma/Medical Devices) 21. Business Analyst (Pharma /Medical Device) and more Keywords: 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.