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Document Management Specialist

West Greenwich, RI
Top 3 Must Have Skill Sets:
    
Microsoft Office (expert level)
Experience working in Manufacturing / Quality Assurance or Quality Control (3 years of experience or more)
GMP experience requires

Description:

Microsoft Office (expert level) Experience working in Manufacturing / Quality Assurance or Quality Control (3 years of experience or more) GMP experience Development of regulated or process documents with the ability to deliver high quality documentation including technical writing. The primary responsibilities may include, but are not limited to the following: Management of Manufacturing process documentation per required process (e.g. Standard Operating Procedure [SOP] on SOPs) in accordance with agreed timelines and in adherence with format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality. Development and facilitation of the creation and/or revision of materials such as SOPs, manuals, and related business process documentation in conjunction with Subject Matter Experts. Note: these activities will usually take place virtually and across different time zones. Liaison with other members of the QCA group (e.g. Business Process Modeler's) and also the business (e.g. Business Process Owner, Document Owner, Authors, Subject Matter Experts). Management of documents via the established Document Review process using the electronic document repository. Track and provide regular updates to process project inventory tool and to key Points of Contact. Requirements include: Experience in developing regulated or process documents with the ability to deliver high quality documentation including technical writing. Sound project management and organizational skills. Ability to work independently and as a team player, demonstrating excellent collaboration and people management skills, preferably to include experience in influencing and negotiation. Experience in leading virtual teams within different regions and cultures. Proficient in discerning, high quality verbal and written communication. Experience of electronic clinical trial/SOP/document systems (e.g., Documentum). Good working knowledge of Microsoft Word. 3+ years’ experience preferably in pharmaceutical industry, with knowledge of quality and compliance Education: Engineering or Scientific background

"This posting is for Contingent Worker, not an FTE"
 

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