Validation/Documentation Specialist

Validation and Documentation Specialist

Our client is growing at a rapid pace! Become a part of their team now and enjoy the success and growth!

This position is responsible for writing, editing, assembling and transmitting all
required validation, operation and maintenance documentation for custom
designed purification equipment. The documentation specialist will be responsible for working closely with the project manager and engineering group to determine the testing and validation requirements for the equipment.

Requirements:
The successful candidate will have an Associates degree in
engineering or another technical area and at least 3 years experience in a
similar position. Person should be familiar with cGMP requirements, validation
of pharmaceutical processes and have a working knowledge of Process Control and
instrumentation. Person must have a demonstrated ability to write user friendly
technical manuals. Must be familiar with Windows-based software packages such
as WORD and EXCEL. Excellent interpersonal communication skills and the ability
to work as a team member are a must!

A working knowledge of FDA validation requirements for software used in the
Pharmaceutical or Biotechnology processing industry would be a plus.




job Requirements


Please refer to the job description above.