Technical Writer P1 (Remote)

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.

Responsibilities:

• 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 c.prince@proclinical.com.

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.

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