Cleaning Validation Engineer – Risk- CQ & CFR

Validation & Engineering Group,Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical,and Medical Devices industries in the following areas:
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services.

• Cleaning Validation is a must
• Expertise in “Risk Based Approach” for Commissioning and Qualification practices
• Planning and Integration of Commissioning and Qualification activities in medical device manufacturing (Class II preferred)
• Equipment qualification and process validation
• 21 CFR Part 11 requirements and how to incorporate these requirements into an efficient testing strategy
• Assist in deviation investigation and resolution for problems and issues encountered during field execution activities

• 3-5 years hands-on validation experience (writing and execution of validation protocols)
• Capable of working independently with minimal supervision, and communicating with project team members to assure timelines are met
• Great technical writing and communication skills
• Proficiency in Microsoft Office application (Word, Excel and Project)
• Effective interpersonal and problem solving skills
• Demonstrate excellence in good documentation requirements and attention to detail

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.

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