Associate I, Quality Control

• The Quality Control Sample Control Group is responsible for QC sample receipt, transport, dispensing, and distribution to the internal and external QC testing labs. The group is also responsible for the custody and management of the Stability Samples. The QC Sample control group is also responsible for the coordination of QC testing in support to technical product complaints.
• The Quality Control Associate I is responsible for supporting key functional, tactical, and operational aspects of the QC group at the Biogen Idec RTP facility. The primary responsibility for a Quality Control Associate I is the execution all activities associated with distribution of QC samples in a cGMP manner. Additional responsibilities include, but are not limited to, basic technical support and problem solving capabilities, basic writing skills, execution of robust and compliant cGMP documentation practices, and a basic understanding of FDA/EMA regulations.

• The Quality Control Associate I will possess demonstrated technical ability regarding fundamental laboratory techniques and analytical methodology. The position requires but is not limited to the following: Understanding of basic biological science principles; ability to communicate with peers and management; effective organizational skills; ability to multi-task and coordinate multiple activities in parallel; developing or demonstrated instrument/method troubleshooting and problem solving skills; general knowledge of FDA/EMA regulations and compliance.

Qualification:

Education B.S. degree (biological science preferred; 0-2 years of relevant experience) or A.S. degree (biological science preferred; 8+ years of relevant experience)

All your information will be kept confidential according to EEO guidelines. 

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-357-1105 ASAP! I want to know more about your preferences.

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