Medical Device Medical Writer jobs
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- Dematic Ltd.Banbury
- We are looking for a Technical Writer who will be working with our Project Management organisation in the UK to create customer-specific operation and…
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View similar jobs with this employerMedical Device Regulatory and Quality Consultant
Often replies in 2 daysPA ConsultingMelbourn- Annual leave
- Company pension
- Private medical insurance
- Cycle to work scheme
- This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
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View similar jobs with this employerMedical Device Regulatory and Quality Consultant
Often replies in 2 daysPA ConsultingMelbourn- Annual leave
- Company pension
- Private medical insurance
- Cycle to work scheme
- This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
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- ArmCambridge
- This role supports concurrent releases of complex silicon IP and system-level platforms, enabling engineers and partners to integrate, configure, and deploy SoC…
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- サイネオス・ヘルスLondon
- Experience working with medical affairs teams.
- In this role, you will help make life science organisations more effective, particularly in complex specialty…
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- ICON PlcReading
- Employee assistance programme
- Company pension
- Reviews Edit Check Plan for appropriate manual and automated medical edit checks and consolidates all medical data review checks.
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- NovartisLondon
- You will work closely with cross-functional partners to support clear, consistent, and scientifically robust product information that enables successful…
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- Michael PageSheffield
- Ensure compliance with medical device regulations, standards, and internal gated processes.
- Minimum 5 years' experience in a technical engineering role within…
- Veeva SystemsRemote
- Work from home
- You will have the opportunity to shape new ways of working in the end-to-end content operating model – from incorporating AI into a tier-based MLR process, to…
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- Veeva SystemsRemote
- As an alternative to an MBA, this program is intentionally designed as the entry path to shape experienced professionals as Business Consultants capable of…
- Veeva SystemsRemote
- Pay rise
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- ReckittSlough SL1 1DT
- Life insurance
- Employee assistance programme
- Experience in HCP content creation / medical writing.
- Would suit an individual with a scientific, sales or medical marketing background who has experience in…
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- OraLondon
- Annual leave
- Company pension
- Private medical insurance
- Well-Being: Offering private medical insurance healthcare beginning day 1 provided by Vitality and SimplyHealth.
- Adhere to all aspects of Ora's quality system.
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- Smith & NephewKingston upon Hull
- Annual leave
- Employee discount
- Company pension
- Paid volunteer time
- Car scheme
- Extensive experience in medical device development, with a strong understanding of the full product development lifecycle, ideally within wound dressings and…
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- Smith & NephewKingston upon Hull
- Annual leave
- Employee discount
- Company pension
- Paid volunteer time
- Car scheme
- Solid experience within Quality Assurance in the medical device or pharmaceutical industry, with working knowledge of ISO 13485, MDR and FDA 21 CFR Part 820.
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Job Post Details
Technical Writer - job post
Banbury
Full-time
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Job details
Job type
- Full-time
Location
Banbury
Full job description
Dematic is a global leader in intelligent automated solutions for warehouses, distribution centres, and manufacturing environments. Our technology powers some of the world’s biggest brands, and our teams help shape the future of logistics. Joining us means working with advanced automation, software, and integrated systems that keep global supply chains moving.
We are looking for a Technical Writer who will be working with our Project Management organisation in the UK to create customer-specific operation and maintenance documentation within customer projects.
We are looking for a Technical Writer who will be working with our Project Management organisation in the UK to create customer-specific operation and maintenance documentation within customer projects.
We offer:
-
Career Development
-
Competitive Compensation and Benefits
-
Pay Transparency
-
Global Opportunities
Tasks and Qualifications:
Key responsibilities:
• Develop high‑quality technical documentation for automated equipment and integrated systems
• Develop high‑quality technical documentation for automated equipment and integrated systems
- Integrate third‑party supplier materials into complete customer documentation sets
- Review and edit content for consistency, usability, and compliance
- Apply and refine documentation standards and structured authoring practices
- Contribute to the rollout of our next‑generation Content Management System
- Ensure all documentation adheres to the EC Machinery Directive and relevant UK/EU standards
- Collaborate with global engineering teams to deliver accurate “as‑built” documentation packages
What We are Looking for:
- Proven experience as a Technical Author/Technical Writer in engineering, automation, manufacturing, or related fields
- Strong ability to translate complex technical information into clear, user‑friendly content
- Hands‑on experience with Content Management Systems (CMS) or Content Delivery Platforms
- Ability to read and interpret technical drawings, schematics, and engineering documents
- Understanding of UK/EU compliance requirements such as the EC Machinery Directive
- Excellent written English and attention to detail
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