Quality Control Analyst II

Genzyme Corporation

Microbiology

July 29, 2010

 

 

Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme's people and culture have been consistently recognized for excellence. For example, we have been named several times to Fortune's list of the 100 Best Companies to Work For in the United States. We also consistently rank among the top employers for scientists in surveys of Science readers. Genzyme's local offices and facilities in Europe and other parts of the world have earned similar distinction as respected employers. By applying for a position with Genzyme, you are taking the first step toward becoming a part of our dynamic and talented team, and sharing in our continued success.
Quality Control Analyst II
Hours: 8:30 am to 5:00 pm Monday to Friday
The qualified individual will join the Quality Control Microbiology Group located in Framingham, MA. This group is responsible for the monitoring of the manufacturing facilities for air and water quality, testing of in-process and final product of several product lines for Quality Assurance release. Job responsibilities include: Participation on the Environmental Action Committees for the Framingham environmental and critical utility monitoring programs.
Write, track and follow up on environmental and critical utility investigations.
Coordinate interdepartmental meetings to facilitate and complete action items required for investigating environmental excusions.
Assist in implementation of corporate policies and maintaining procedures current with industry standards for facility investigations.

 

 

 

Basic Qualifications: Bachelor's Degree with a minimum of 2-4 years Quality experience in an investigation role.
Preferred Qualifications:
This candidate should possess strong computer skills for the utilization of LIMS and data trending. Strong communication skills are required. cGMP knowledge preferred.

 

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