Regulatory Specialist
2 weeks ago
Adecco LifeSciences are proud to be partnering with a global manufacturing leader within the Medical Devices industry.
Reporting to the Regulatory Manager you will help build and sustain Regulatory systems and processes and work closely on the collation of technical files for MDR compliance and global product submissions into the EU and US.
Requirements for this position include:
Maintenance and collations of technical files, providing updates where required for product approvals, CE declarations and MDR compliance.
Experience of global product submissions (EU essential)
Working on UKCA marking activities
Knowledge of MDR and related legislation including ISO 13485, ISO 14971.
The company are looking to hire someone who is keen to continue their personal development as a Regulatory Specialist.
Offering a hybrid working arrangement, with 2 days needed onsite per week.
Looking for someone to start ASAP, if you are interested please get in touch.
Adecco Lifesciences is acting as an Employment Agency in relation to this vacancy.
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