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Job Details

QA Document Management Specialist – Global Biotech – UK, Cambridge – 12 Month Contract – £30 - £37 per hour

Company: Meet
Location: Cambridge
Reference: MD-AM-DocMan-1
Closing Date: 07 Sep 18
Type: Contract
Salary (£): Negotiable

Job Summary:

A leading biotech in Cambridge are looking for a QA Document Management Specialist to join their site on a 12 month contract basis as part of a major R&D project. For further details please contact Matt Dixon on 0203 019 6006 or email


A global biotech is looking for a diligent QA Document Management Specialist to join their site in Cambridge as part of a major R&D Project. They are offering a 12-month contract for successful applicants.

The role will focus on the development of regulated or process documents with the ability to deliver high quality documentation, including technical writing. This position will support the management of R&D controlled processes and the generation and/or revision of associated documents.


Company Background

This company are a global biotech located in Cambridge, just under an hours journey from London by train.

This position represents an opportunity to work for a pioneer in biologic therapies. A company that discover, develop and deliver innovative human therapeutics.

As a member of the R&D Quality Compliance and Audit group, you will be responsible for supporting the development of controlled documentation for R&D processes.

Get in touch with Matt Dixon at or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.


Role Responsibilities

Working as a QA Document Management Specialist your main responsibilities will be:

  • Management of R&D process documentation per the required processes (e.g. SOPs) in accordance with project timelines and in adherence with compliant formatting, considering usability, accuracy, consistency and quality. 
  • Creating and/or revising of materials such as SOPs, user 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. 
  • Liaise 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


Skills Required

  • Advanced degree in science, pharmacy, biological science or related field is preferred.
  • Experience in developing regulated/ process documents to a high level including technical writing 
  • 3+ years’ experience preferably in R&D/pharmaceutical industry, with knowledge of quality and compliance
  • Experience of electronic clinical trial/SOP/document systems (e.g., Documentum)
  • Ability to work independently and as a team player, demonstrating excellent collaboration and people management skills, preferably to include experience in influencing and negotiation
  • Sound project management and organizational skills
  • Good working knowledge of Microsoft Word

Get in touch with Matt Dixon at or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.


Commutable Locations: UK, Cambridge.

Rate:  £30-£37  

Full job description and company details are available upon application, apply below. The position is being dealt with by Matt Dixon at Meet, call us on 0203 019 6006 or email directly at to discuss in confidence.

Meet are good people wo are great at recruitment. We’re proud to partner with the industry’s leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.

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Apply for this job: QA Document Management Specialist – Global Biotech – UK, Cambridge – 12 Month Contract – £30 - £37 per hour

Contact Information:

Address:  meet
Irongate House, 30 Dukes Place, London
Tel:  +44 203 178 7488
Website:  Visit Our Web Site

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