Author Jobs in Stevenage
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Search results - Author Jobs in Stevenage
Stevenage
Astute's Team is partnering with a leading provider of Technical Publications to global OEMs, to recruit a Technical Author for the Nuclear Sector.
The Technical Author role comes with a salary of up to £48,000, private medical insurance, life...
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cv-library.co.uk -
MBDA-Stevenage
Job Description
Stevenage
An opportunity has arisen in the transforming Technical Publications department within MBDA. The purpose of this roles is to analyse, develop and deliver the Technical Publications for a complex portfolio of MBDA's...
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Apsida Life Science-Stevenage
to source, interpret, and integrate data into documents.
• Author and finalize briefing books and related documentation for scientific advice meetings (e.g., FDA, EMA, national health authorities) to support development programs and address regulatory...
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Outlier-Stevenage
Job Description
Earn up to $16 USD/hourly and work fully remotely and flexibly. Outlier, a platform owned and operated by Scale AI, is looking for English speakers to contribute their expertise toward training and refining cutting-edge AI systems....
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Skills Alliance Enterprise-Stevenage
trackers.
• Author, review, and approve GxP documentation.
• Act as a QA representative supporting the Pharmaceutical Quality System (PQS), including oversight of change controls, deviations, complaints, QC invalids, OOT/OOS results, and environmental...
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MBDA-Stevenage
Stevenage
An opportunity has arisen in the transforming Technical Publications department within MBDA. The purpose of this roles is to analyse, develop and deliver the Technical Publications for a complex portfolio of MBDA's products across the Air,...
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jmmst.com -
Planet Pharma-Stevenage
including vendor management
• Apply good publication practices and ensure compliance with global SOPs and documentation requirements
• Review publication drafts for scientific quality and alignment with author direction
• Track budgets, report on progress...
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Stevenage
this opportunity may be for you. As a Software Architect, you will play a crucial role in designing innovative solutions and ensuring the integrity and robustness of software systems within the defence sector. You will be the author of the entire software...
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cv-library.co.uk -
The RFT Group-Stevenage
Medical Affairs, etc.
The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures, clinical study reports and clinical summaries, and regulatory development documents...
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Randstad-Stevenage
development teams to support new product development and change control, ensuring compliance with US, EU, and other global regulatory requirements.
• Author EU technical documentation under MDR, FDA submissions (e.g., 510(k)) and other global regulatory...
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MBDA-Stevenage
As a Software Architect, you will be the author of the full software architecture working with the software delivery teams to define and monitor the Structural and Temporal Architecture including the Internal/External interfaces of the product to meet...
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mindmatch.ai -
The RFT Group-Stevenage
Operations, Regulatory Affairs, Medical Affairs, Commercial, etc.
The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures, clinical study reports and clinical...
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MBDA-Stevenage
issues in a timely and detailed way.
Analyse data : Record and meticulously analyse trial data to verify that the actuator meets its stringent requirements.
Report findings : Author comprehensive trial conduct reports to support the product's...
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joblookup.com -
Aqua Consultants-Stevenage
to excellent time and quality
• Analyse data to produce trends and drive decision making
• Organise meetings and workshops with clients
• Author reports and presentations to enable informed decision making for the client and internal teams
• Contribute...
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The RFT Group-Stevenage
intelligence to internal stakeholders and assist in preparing the organization for any internal adaptation that may be required.
Author, review, and update RA SOPs as needed, with emphasis on clinical regulatory processes.
Maintain links with external...
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