Research & Development Assoc I

  • location: Research Triangle Park, NC
  • type: Contract
  • salary: $22.67 - $27.45 per hour
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job description

Research & Development Assoc I

job summary:
As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!

location: Durham, North Carolina
job type: Contract
salary: $22.67 - 27.45 per hour
work hours: 9 to 5
education: Bachelors
The QC Associate I is responsible for supporting key functional, tactical, and operational aspects of the QC Microbiology group. Performs testing, and all associated activities associated with this testing. Responsibilities include, but are not limited to, training, testing support, support for qualification/validation/certification activities as appropriate, robust and compliant cGMP documentation practices. A fundamental understanding of the Quality Systems and able to apply it in their daily support functions. Adherence to all GMP requirements, effective interactions/communication with Quality management, personal development, and support of investigations. Able to work effectively within the group.

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/EMEA regulations and compliance
  • 0-2 years of relevant experience (B.S. degree) OR 2+ years of relevant experience (A.S. degree).
skills: Quality control, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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