Regulatory Affairs Quality and Project Management
Regulatory Affairs/Quality & Project Specialist - IVD/Med Dev - East Midlands - £competitive
This start up company are in a growth phase and are looking to further strengthen their team. With considerable expertise within the business already this IVD company are now looking to recruit an outstanding Regulatory Affairs/QMS specialist for this newly created position. You will be responsible for supporting all regulatory activities, keeping track of requirements for product registrations and work closely with product teams to ensure products and documentation meet compliance requirements.
The ideal candidate will have a degree in a medical/biosciences- related subject plus further education or proven work experience in Regulatory Affairs. You will be highly motivated, driven and creative with excellent interpersonal, communication and organisational skills. Working knowledge of QMS and ISO13485 is essential. You will be a real people person and expect to join a welcoming, professional and respectful team. You will be able to collaborate cross-functionally and be experienced in Regulatory Submissions and Project Support. You will be open to travel within the UK and overseas. The role is flex as to base location but with that will come a willingness to travel to various UK company sites. You will have excellent project planning and project management skills and will be motivated to really make this your own.
To apply for this role or to have a confidential discussion please contact Deborah on 01480 275527 or e-mail email@example.com
Key words - Regulatory Affairs, Quality - 13485 - Project - IVD - QMS - East Midlands
Delta Consultants - Scientific and Medical Recruitment - Applying the Art of Recruitment Science
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Delta Consultants Ltd is acting as an Employment Agency in relation to this vacancy.
- Required Skills
- Regulatory Affairs, Quality - 13485 - Project - IVD - QMS - East Midlands