Validation & Engineering Group, Inc.
LL01-062824 Validation Specialist (NC)
Validation & Engineering Group, Inc., Raleigh, North Carolina, United States, 27601
Validation & Engineering Group, Inc.
V&EG is a leading services supplier providing solutions to the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the areas of Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
About the Role We are seeking talented, dedicated individuals committed to the highest standards of ethics with expertise in the following areas:
Process Equipment and Utilities IQ/OQ
Computer System Validation (CSV)
Experience with the qualification of several of the following equipment and processes:
HVAC, environmental monitoring, Laminar Flow Hoods, CIP/SIP skids, Freezers, Parts Washers, Autoclaves, Isolators, Vacuum Pumps, Debagger, Delidder, Syringe Filling Machines, Syringe Inspection, Peristaltic Pumps, Gas Monitoring, Filter Integrity Testers, VHP Generators, Material Transfer Isolators, Check Weighs, Portable Tanks, Oxygen Sensor, Heat Exchangers, PH Meter, TCU, Scales/Balances, Sterilization and decontamination processes with VHP generators, Automation Control Systems, BAS systems.
Able to work independently.
Qualifications
Bachelor's Degree in Science or Engineering
Minimum of 4 years of experience in direct pharmaceutical, medical device or biotechnology industries.
Experience in IOQs within direct process / manufacturing areas.
Must be proficient using MS Windows and Microsoft Office applications.
Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance, i.e. FDA guidelines, cGMP, 820, OSHA, 21 CFR Part 11, and other related CFR's, ISPE Good Automated Manufacturing Practice (GAMP).
Kneat experience valuable.
Seniority level: Mid‑Senior level.
Employment type: Full‑time.
Job function: Strategy/Planning and Information Technology.
Referrals increase your chances of interviewing at Validation & Engineering Group, Inc. by 2x.
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About the Role We are seeking talented, dedicated individuals committed to the highest standards of ethics with expertise in the following areas:
Process Equipment and Utilities IQ/OQ
Computer System Validation (CSV)
Experience with the qualification of several of the following equipment and processes:
HVAC, environmental monitoring, Laminar Flow Hoods, CIP/SIP skids, Freezers, Parts Washers, Autoclaves, Isolators, Vacuum Pumps, Debagger, Delidder, Syringe Filling Machines, Syringe Inspection, Peristaltic Pumps, Gas Monitoring, Filter Integrity Testers, VHP Generators, Material Transfer Isolators, Check Weighs, Portable Tanks, Oxygen Sensor, Heat Exchangers, PH Meter, TCU, Scales/Balances, Sterilization and decontamination processes with VHP generators, Automation Control Systems, BAS systems.
Able to work independently.
Qualifications
Bachelor's Degree in Science or Engineering
Minimum of 4 years of experience in direct pharmaceutical, medical device or biotechnology industries.
Experience in IOQs within direct process / manufacturing areas.
Must be proficient using MS Windows and Microsoft Office applications.
Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance, i.e. FDA guidelines, cGMP, 820, OSHA, 21 CFR Part 11, and other related CFR's, ISPE Good Automated Manufacturing Practice (GAMP).
Kneat experience valuable.
Seniority level: Mid‑Senior level.
Employment type: Full‑time.
Job function: Strategy/Planning and Information Technology.
Referrals increase your chances of interviewing at Validation & Engineering Group, Inc. by 2x.
#J-18808-Ljbffr