Validation Manager Job
My client is a leading provider of drug development and manufacturing services to pharmaceutical, biotech and medical device companies around the world. The company is experiencing many exciting changes including lab renovations and commitment to growth within contract development and manufacturing. Because of this they are in need of a Validations Manager in one of their Southeast facilities.
The ideal candidate will be a hands manager with experience in a pharmaceutical GMP aseptic environment. They will be responsible for management of reviewing and revising of SOP’s, supporting facility, utility and manufacturing equipment as well as cleaning and process validation projects at company or vendor sites.
Qualifications:
· Bachelors with 6+ years of experience in a pharmaceutical GMP aseptic environment and 3+ years of supervisory experience is a must.
· Require strong knowledge of quality assurance and/or engineering author, review, and execution of validation protocols, cGMP training and knowledge, and excellent communication and computer skills.
· CQE certificate and active member of ISPE a plus.
Send Resume to:
Kim Thompson
kim@fpccareers.com