We are seeking a Sr Quality Specialist to join a leading Pharmaceuticals company in Boston, MA. The chosen individual would be joining the Quality Standards, Training and Improvement department, and would be responsible for performing multiple activities in support of their group or clients. This is an onsite opportunity that is offered on an initial 6 month contract basis, with potential to extend/convert. As a w2 contract worker you are eligible to a competitive hourly rate, health/dental/vision/life insurance, a 401k vehicle and more.
Responsibilities:
· Presents a solid understanding of quality assurance concepts and practices
· Demonstrates knowledge of applicable regulations and the interpretation and application of regulations and compliance concepts related to document control
· Responsible for all GxP Archiving Activities and regulatory knowledge
Requirements:
· B.S. in a scientific or allied health field (or equivalent degree) and 3 - 5 years of relevant work experience, or
· Experience working in Electronic Document Management Systems (Doc Compliance, Veeva, Documentum, etc)
· Proficient in Microsoft Office programs, technical writing skills
Please apply with your most up to date resume to be considered.
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