Technical Writer P1

4 weeks ago

Hertfordshire, United Kingdom Proclinical Full time

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.

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.

QACompliance

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