Associate I, Quality Control at Real in Raleigh, NC

Company Description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognizing talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description

• 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.

Qualifications

• 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)

Additional Information

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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