What are the responsibilities and job description for the Validation Specialist - SC position at Validation & Engineering Group Inc.?
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas : Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position :
Manufacturing, Packaging and Laboratory Equipment
Commissioning / Qualification
Process Validation
Cleaning Validation
Periodic Reviews
Qualifications :
Bachelor's Degree in Science or Engineering.
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.
Experience in 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.
Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
Risk Assessments.
Periodic Reviews
Technical Writing skills and investigations processes.
Available to work extended hours, possibility of weekends and holidays.
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