Validation Engineer / SpecialistJob Code: C&Q
Category: Validation Engineer or Specialist
Location: ALL Areas
Openings throughout the United States, Europe and Asia.
The Validation Engineer/Specialist will support the biotech, pharmaceutical, and medical device industries. Responsibilities include development of documentation to support validation such as user requirements specifications, enhanced design review, commissioning and qualification protocols. The employee will also be responsible for protocol execution and field verifications, as well as summary report writing. This position requires excellent communication skills, the ability to learn and work in a fast paced environment, and knowledge of good documentation practices. Experience with bio-pharma manufacturing systems, utilities, and cleaning validation is a plus.