Regulatory Technical Author
Regulatory Technical Author
Posted on :
20-01-2025
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1 Vacancy
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Job Description
Job Title: Regulatory Technical Author
Job Location: Amersham UK
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level:
Be part of something altogether lifechanging!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake lifesaving activities ranging from fundamental biological research to developing innovative vaccines new medicines and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other our customers and their patients. With associates across 40 countries Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher we bring together dedicated technical expertise and talent to develop the next generation of lifechanging therapeutics.
The Regulatory Technical Author for Cytiva is responsible for writing the documents supporting our regulatory strategy
This position is part of the Regulatory Science & Strategy located in Europe / USA and will be fully remote. At Cytiva our vision is to advance future therapeutics from discovery to delivery.
What you will do:
Join our winning team today. Together we’ll accelerate the reallife impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges architecting solutions that bring the power of science to life.
For more information visit
At Danaher we value diversity and the existence of similarities and differences both visible and not found in our workforce workplace and throughout the markets we serve. Our associates customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake lifesaving activities ranging from fundamental biological research to developing innovative vaccines new medicines and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other our customers and their patients. With associates across 40 countries Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher we bring together dedicated technical expertise and talent to develop the next generation of lifechanging therapeutics.
The Regulatory Technical Author for Cytiva is responsible for writing the documents supporting our regulatory strategy
This position is part of the Regulatory Science & Strategy located in Europe / USA and will be fully remote. At Cytiva our vision is to advance future therapeutics from discovery to delivery.
What you will do:
- Plan execute and edit documentation related to regulatory supporting the products through their lifecycle.
- Review and edit Ad Promo documents in the Cytiva document management systems
- Take part in continual improvement workshops related to documentation management
- Be part of cross functional teams to support projects at global level and coordinate documentation between departments including R&D Operations Marketing and Quality/Regulatory teams.
- Adhere to the company’s Style Guide terminology guidelines and relevant bestpractice guidelines
- Experience in quality technical writing in the biotechnology field or related discipline
- Excellent communication writing and grammar skills in the English language at the nativespeaker level
- Comfortable acting as SME and making decisions on behalf of the team.
- Holds strong commitment to quality and continuous improvement is willing to act and able to influence others
- Proven problemsolving skills and attention to detail
- Ability to travel – 15% domestic and international overnight travel within Europe and USA
- Must have a valid driver’s license with an acceptable driving record
- Regulatory compliance aspects of maintaining document conformity such as the USP RoHS REACH directives.
Join our winning team today. Together we’ll accelerate the reallife impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges architecting solutions that bring the power of science to life.
For more information visit
At Danaher we value diversity and the existence of similarities and differences both visible and not found in our workforce workplace and throughout the markets we serve. Our associates customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
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Employment Type
Full Time
Key Skills
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