Validation Specialists/ Project Managers- Maryland/ Northeast

For over 10 years cGMP Validation LLC has provided innovative and cost effective validation solutions for leading Biotechnology/ Pharmaceutical companies in the U.S. and around the world.

 

We have IMMEDIATE OPPORTUNITIES for Validation Specialists and Project Managers to join our dynamic team in Maryland, Virginia and the Northeast.  Successful candidates will be highly motivated, possess strong communication skills and have the desire to grow with the company.

 

Qualifications for VALIDATION SPECIALISTS: Validation experience in one or more of the following areas: automation, equipment, utilities, laboratory instruments, and/ or computerized systems. Experience authoring SOPs or other technical documents Bachelors Degree or equivalent work experience in Engineering, Computer Science, Information Systems, or Life Sciences. Knowledge of FDA regulations and guidelines, including cGMP’s and 21CFR Part 11 Good oral, written and interpersonal skills













Qualifications for PROJECT MANAGERS: In addition to above, successful PMs must have experience managing small to medium size validation projects within budget Ability to quickly understand technical/ scheduling/ compliance issues and provide solutions to clients Highly organized and skilled at using MS Project



cGMP Validation is staffed with professionals of considerable experience and diverse educational disciplines.  Consequently we offer a broad portfolio of validation and compliance services for the pharmaceutical, biotech, medical device, and medical diagnostic industries.  cGMP Validation's clients have ranged from the largest multi-national corporations to small biotechnology startups.

 

We welcome you to submit your resume today to join our growing team!

 

To learn more about us, please visit our website at: http://www.cgmpvalidation.com