Validation Specialist Associat-32005
Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to making a positive impact on the lives of the patients and families we serve. Genzyme's portfolio of transformative therapies, which are marketed in countries around the world, represent groundbreaking and life-saving advances in medicine. As a Sanofi company, Genzyme benefits from the reach and resources of one of the world's largest pharmaceutical companies, with a shared commitment to improving the lives of patients. Learn more at www.genzyme.com.
Validation Specialist Associate
The Validation Specialist I position is responsible for performing qualification of general manufacturing equipment, for executing PQ's for processes such as CIP and SIP, for performing autoclave cycle validations, and for executing routine requalifications. The candidate is expected to work with minimal supervision and to schedule validation activities with Manufacturing personnel. The candidate will prioritize projects in consultation with his manager, and may require general guidance on protocol methodology. However, the candidate is also expected to draft and execute Validation studies in accordance with current guidance documents independently.
The basic qualifications are a BS degree in a scientific discipline and 1-2 years experience, or an associate's degree in a technical discipline and 3-5 years experience in a GMP environment.
Job : Quality
Primary Location : United States-Massachusetts-Framingham
Job Posting : Jan 6, 2013
Shift : Day Job
Job Type : Regular
Employee Status : Regular