Document Quality Controller

Our major pharmaceutical client in Indianapolis is looking for a document controller to join their Quality Systems team.

Payrate: $24.00/hr

Responsibilities include:

• Manage Quality System documents through preparation, review, approval and maintenance processes in order to meet business and compliance needs
• The above activities would mainly focus on routine processing tasks to include (but not limited to) document deletions, abbreviated approvals, targeted changes, and processing of business practice documents
• Ability to manage multiple deliverables/documents to ensure accurate and timely implementation, often within aggressive deadlines.

Shift: Monday-Friday, 8am-5pm

Keywords provides a competitive compensation package, good benefits and a casual, fun, productive and supportive working environment. We empower people to perform to the best...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Documentation Specialist based onsite in our Andover, MA facility.  CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.  CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Quality Control Documentation Specialist is responsible for performing the data review for the release of regulated and/or non-regulated materials including raw materials, in-process and finished...