Operational QA Advisor

  • Company: GSK
  • Location: Pennsylvania, United States
  • Posted: December 21, 2017
  • Reference ID: WD149921
Why You?

Basic qualifications:
• Bachelor's degree in a science discipline (preferred) or equivalent combination of specialized training and relevant work experience.
• Previous experience of GMP documentation reviews with strong attention to detail

Preferred qualifications:
• Ability to work under pressure in an environment where a range of issues will pull upon your time and where there are likely to be conflicting priorities.
• Experience of range of dosage forms including sterile products or experience in packaging
• Knowledge of the R&D process, particularly with respect to clinical trials manufacturing and packaging.
• Demonstrated ability to function effectively as part of a team; to communicate effectively with all levels of management and to negotiate persuasively.
• Demonstrated ability to work independently; to set priorities, meet deadlines and handle a high volume of work.
• Demonstrated ability of third party auditing of starting materials, API and finished product suppliers and contractors would be highly desirable

Why GSK?:
At GSK, our mission is to improve the quality of human life by enabling people to do more, feel better and live longer. Our three world-leading businesses research and deliver innovative medicines, vaccines and consumer healthcare products. We need a talented and motivated workforce to deliver against our strategy. To achieve this, we strive to attract the best people and to create an environment that empowers and inspires.

Contact information:

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