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Biotech Document Controller
Cosham, Hampshire
Salary: Negotiable
Job Type: Temporary
Start Date:
Job Reference: 212962
Added: 10 Sep 2020
Job Description

Biotech Document Controller

A unique opportunity has arisen for a Biotech Document Controller for a global leader in the Life Sciences industry.

The main purpose of this role is to oversee the business management system controls which approximately supports 10,000 regulatory documents for global products and customers. Your goal will be to open this system customers in a self-serve portal environment. 40 hrs per week for 10 month contract

Essential job functions:

  • To scrupulously evaluate existing regulatory documentation within our electronic system to ensure the documentation is titled and filed correctly.
  • To collect missing regulatory claims and compliances on components and finished articles from within the company and our third-party suppliers.
  • To liaise with subject matter experts to verify correctness of information and titles.
  • To support product managers in the requirements and upload of their product documents.
  • To liaise with subject matter experts to verify correctness of information and titles.

Minimum Qualifications:

  • HNC or higher qualification in Biology, Quality/Regulatory Control, Business Administration, Computer Science or similar field.
  • Minimum of 3 years' experience working with regulatory documentation.
  • Experience in working with WEB based documentation systems.
  • Experience and knowledge of working with Biotech/Scientific/Medical Documents

Person specification

  • Good eye for detail and accuracy
  • Data research and analysis skills
  • High level of patience and focus
  • Persistent in driving through an action to a resolution
  • Good written and spoken English language communication skills
  • The ideal candidate must be a self-starter and capable of working independently and in a team

This is a 10 month contract, 40 hours per week.

Please send your CV to or apply online

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