Regulatory Affairs Specialist Jobs

Key skills and experience for the Regulatory Affairs Specialist: Relevant food science/food law qualifications and/or experience in a related field ideally coupled with experience in a regulatory affairs working environment Keen...

Company description: Mller UK & Ireland is wholly owned by the Unternehmensgruppe Theo Mller which employs over 24,000 people throughout Europe. In the UK, Mller develops, manufactures and markets a wide range of branded and private...

As Regulatory Affairs Specialist , you will have: Key Skills: Previous experience in regulatory affairs in the medical device industry Knowledge of UK, EU, US regulations, standards and guidelines Experience with compiling If you feel...

Join Our Team as a Regulatory Affairs Specialist We are currently recruiting for Regulatory Affairs Specialist in the UK . The Regulatory Affairs Specialist will be responsible for regulatory activities in support of lifecycle...

Regulatory Affairs Associate 12 Month FTC Cheshire (Hybrid) up to £40,000 Benefits REF 1926 I am currently recruiting for a Regulatory Affairs Associate to work for a leading engineering organisation based in Cheshire, but on a hybrid...

Since 2019, the Group has made seven acquisitions: Sealantis, an Israeli developer of innovative internal sealants, Biomatlante, a French developer and manufacturer of surgical biomaterials, Raleigh, a leading UK coater and AMSs...

Job Description: We have an opportunity for a Senior Scientific and Regulatory Affairs UK/IRL Market Lead (known internally as Program Manager SRA (Science & Regulatory Affairs) UK/IRL) to join us at Mars. You will lead a variety of...

Key Activities / Key Responsibilities: Lead regulatory strategy and submission preparation for Safety and some CMC variations for solid, liquid and parenteral formulations in Europe, UK and Switzerland Review and update outdated...

Reporting to the Regulatory Affairs Manager, you will play a key role in supporting global regulatory submissions, maintaining compliance documentation, and ensuring adherence to regulatory standards for medical devices in the EU,...

For this role you would require the following experience: 10 years experience across regulatory affairs (strategy through to artwork) Broad exposure to product lifecycle management in Europe (Small Molecule) Experience with MAT,...