24N/QUAL – Quality AND Technical Writer

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Full time
Location: London
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Job offered by: Randox Laboratories
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Category:
Quality and Technical Writer - (Job Ref:24N/QUAL)

At Randox, we are seeking an experienced Quality and Technical Writer to join our team. The ideal candidate will be responsible for producing high-quality technical documentation that is accurate, concise, and easy to understand. As a quality and technical writer, you will work closely with cross-functional teams to ensure all technical documents, manuals, and instructions meet company standards and comply with industry regulations.

This role will be based at our Science Park at Antrim.

Responsibilities: Write and maintain technical documents, including user manuals, SOPs, and training materials. Collaborate with subject matter experts and cross-functional teams to develop and maintain technical documentation that meets customer and regulatory requirements. Ensure all technical documents adhere to company standards, including style, format, and quality. Perform quality assurance reviews on technical documents to ensure accuracy and completeness. Revise/update technical documentation based on changes in products, processes, or regulations. Conduct research and gather information from various sources to produce technical documentation that is accurate and complete. Work with the team to develop processes and procedures to improve efficiency.

Essential:

HNC/HND/Degree in Engineering/Technical Writing/English or experience in technical writing, preferably in a regulated industry. Excellent writing, editing, and proofreading skills with good attention to detail. Knowledge of industry regulations and standards. Proficiency in Microsoft Office, Adobe, and other document management tools. Strong communication skills and ability to work collaboratively with cross-functional teams. Ability to work independently and manage multiple projects.

Desirable:

Minimum 3 years of experience in technical writing, preferably in a regulated industry. Previous experience in an engineering or diagnostic medical company. Experience in a controlled manufacturing analytical environment.

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