Senior Regulatory Affairs Associate contract job
2 weeks ago
Our client is a globally recognised leader within the medical devices space. With a strong presence in over 100 countries, they are renowned for producing cutting-edge research and innovative solutions that have greatly impacted patients lives around the globe.
Oversee and ensure all regulatory affairs are compliant with global standards.
Develop and implement regulatory strategies for new and existing products.
Maintain regular communication with regulatory bodies.
Coordinate and manage regulatory submissions.
Conduct regulatory risk assessments and implement mitigation strategies.
Collaborate with cross-functional teams to ensure regulatory compliance throughout product lifecycle.
Provide expert regulatory advice to the team and management.
Keep up-to-date with changes in regulatory legislation and guidelines.
A successful Senior Regulatory Affairs Associate should have:
A degree in Life Sciences or a related field.
Proficiency in regulatory affairs and compliance within medical devices (MDR experience is essential)
UK remote working with monthly travel to site (Glasgow)
Competitive salary and benefits package
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