UK CW Document Management Specialist

A contract opportunity has opened for a UK CW Document Management Specialist to work for an innovator in biologic therapies, who discovers, develops, and delivers ground-breaking human therapeutics.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• Management of R&D 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.
• Communicate with other members of the QCA group (e.g. Business Process Modellers) and also the business (e.g. Business Process Owner, Document Owner, Authors, Subject Matter Experts).
• Management of documents via the established R&D Document Review process using the electronic document repository (EDM Quality).
• Track and provide regular updates to process project inventory tool and to key Points of Contact.

Key Skills:

• Excellent project management and organisational 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.

Requirements:

• At least 3+ years' experience preferably in R&D/pharmaceutical industry, with knowledge of quality and compliance.
• Experience in developing regulated or process documents with the ability to deliver high quality documentation including technical writing.
• 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.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.