GMP Quality Assurance Specialist: Cambridge Isotope Labs, Inc.

Cambridge Isotope Laboratories, Inc. is the world’s premier producer of stable isotope labeled compounds and the world leader in the field of stable isotope separations. For more than 25 years, CIL has specialized in the development, production, and marketing of stable isotopes and chemical compounds labeled with stable isotopes. Join us for excellent career opportunities as we drive the expansion of market application with innovative product development. Want to learn more? Visit us at our website: www.isotope.com

GMP Quality Assurance Specialist

Outstanding opportunity to enhance your career in the GMP Quality Assurance field and be part of a GMP environment responsible for the quality of several new and existing active pharmaceutical ingredients (APIs).

As the QA Specialist, you will be primarily responsible for the review of executed batch records and deviations. You will participate in internal audits and help maintain our vendor/supplier and raw material qualification program.

The GMP Quality Assurance Specialist will also aid in performing other Quality Assurance functions as appropriate (document writing/revisions, CAPA’s, line clearances, continuous improvements and other administrative duties as needed).

This position requires a BS in Chemistry or related science with a minimum of 2 to 5 years experience with Quality Assurance in a biotech or pharmaceutical cGMP setting. Knowledge and/or experience in regulatory affairs and ISO is a plus. The successful applicant will be detailed-oriented, possess excellent verbal and written communication skills, good interpersonal and organizational skills and be a team player.

CIL offers a very competitive benefits package including health, dental and life insurance, 401k Plan and sabbatical program.

Please email your resume to: humanresources@isotope.com

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