Hobson Prior is seeking a Technical Documentation Specialist to join a dedicated team. This role will focus on creating and managing important documents related to medical devices, ensuring they meet European standards. The successful candidate's expertise will be crucial in maintaining compliance and supporting product registration processes.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Create and update technical documents to meet European regulations.
- Offer guidance on relevant standards and rules.
- Prepare and submit changes for approval by authorities.
- Improve processes for product registration and related tasks.
- Ensure timely collection of documents needed for importing/exporting products.
- Handle administrative tasks for product registration.
- Communicate with various partners about ongoing registrations.
Key Skills and Requirements:
- Experience in creating technical documents for medical devices.
- Located in Frankfurt or open to relocating there.
- Strong organisational and communication skills.
- Ability to work well in a team as well as individually.
For more information, please contact Toby Shelton.
Apply now
If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By providing your details and submitting this form you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.
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