Technical Writer P1 (remote)

Highly Competitive
  1. Contract
  2. Good Pharmacovigilance Practice (GVP)
  3. United Kingdom
Hertfordshire, England
Posting date: 31 Jan 2024

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting for a Technical Writer P1 to join a consultancy. This role is on a contract basis with the ability to work remotely from anywhere in the UK.


  • You will verify quality system architecture precision and constancy of content in and between linked documents.
  • Assist the MQO quality systems with editing, quality checks, and data integrity evaluation.
  • Guarantee the precision and accomplishment of document control records, which involves document revision histories, revisions, approvals, and linked metadata.
  • Handle actions both effectively and proactively to accomplish timelines.
  • Collaborate with the global patient safety team to collate information and incorporate feedback into the SEQS document development.
  • Other duties may be assigned.

Key Skills and Requirements:

  • Educated to a degree level in a pertinent discipline, for example: technical writing or life sciences.
  • Demonstrable experience within technical writing, focusing on GVP-linked documents or similar positions within a biotech or pharmaceutical organisation.
  • Familiarity using Veeva QualityDocs or any other electronic document management systems would be ideal.
  • An organised individual with a high attention to detail.
  • Interpersonal and communication skills both verbally and in writing.
  • Capable of handling various projects and priorities concurrently.
  • Works well both independently as well as in a team.

If you are having difficulty in applying or if you have any questions, please contact Connie Prince at

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.