Document Management Specialist
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Location
Berkshire, England
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Sector:
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Job type:
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Salary:
Negotiable
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Contact:
Matt Thomas
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Contact email:
matt.thomas@pharma-partners.co.uk
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Job ref:
23003_1615366764
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Published:
about 1 year ago
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Expiry date:
2021-03-31
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Consultant:
#
Job title: Document Management Specialist
A global Pharmaceutical company with offices in Berkshire are seeking a Document Management Specialist to join on a contract basis.
Responsibilities:
- Under tight timelines, lead and/or facilitate the writing, review, revision, and formatting/QC of controlled documents; while adhering to format, content and style guidelines, considering usability and ensuring accuracy, consistency and quality according to templates and style guide
- Transform subject matter expert and stakeholder discussion and/or process model flows into written controlled document procedures.
- Develop, write, edit, and format materials such as Standard Operating Procedures, Work Instructions, and related business process documentation. When creating/revising the documentation, follow internal procedures (eg, Style Guide and checklists)
- Additionally, this position will be required to process documents via the established Research &Development (R&D) electronic document repository (Veeva Vault - CDOCs)
Requirements:
- At least 3 years prior experience specifically as a technical/business writer for writing controlled process documentation (eg, SOPs, user manuals) in the bio/pharma or medical device industry (other regulated environments may be considered)
- MS Outlook, (advanced) Word, Excel, and electronic document management repositories. MS Project and Visio experience preferred.
- Candidate should have critical thinking skills who is able to work independently with little direction.
A 12-month contract with a competitive hourly/day rate is in offer.
To apply for this position or hear further details then please contact Matt Thomas via matt.thomas@pharma-partners.co.uk
