Regulatory Affairs Senior Specialist - International in London

Regulatory Affairs Senior Specialist - International in London

London Full-Time No working from home possible
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Regulatory Affairs Senior Specialist - International Location: Bedford The Vacancy Swiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD is a joint venture between

Procter & Gamble (P&G)

and

Abbott ; and our brand

Clearblue , is recognised worldwide for delivering accurate home pregnancy and fertility monitoring tests. We are looking for a

Senior Regulatory Affairs Specialist

to join our Regulatory Affairs International team on a

Full-Time, Permanent Contract . The role will be based at our Innovation Centre in

Bedford, UK

with an option for

Hybrid Working . The Senior Regulatory Affairs Specialist - International role leads the delivery of

regulatory strategies for international markets, product registrations and business growth initiatives . Reporting to the Regulatory Affairs Manager - International, the role plays a key part in supporting product launches, market access and ongoing compliance across a diverse range of global territories. The role provides

expert regulatory guidance and technical expertise

for the registration, maintenance and lifecycle management of medical device and IVD products across regions including CIS, Asia, the Middle East, Africa and other emerging markets. This includes assessing regulatory requirements, supporting market expansion opportunities and advising on the impact of product, manufacturing and labelling changes. Working closely with internal stakeholders and external regulatory partners, distributors and consultants, the successful candidate will lead

complex international registration activities

and help deliver compliant, practical and commercially effective solutions that support growth in existing and new markets. We're looking for someone with a

degree in a relevant life sciences discipline (or equivalent experience)

and extensive experience within the

Medical Device and/or IVD industry . Candidates should have a proven track record of successful international product registrations, strong knowledge of global regulatory frameworks and experience developing regulatory strategies that support international market access. Strong project management, analytical and stakeholder management skills are essential, along with the ability to communicate complex regulatory requirements clearly and provide strategic recommendations that support business objectives. Experience managing regulatory consultants, distributors and external partners would be highly advantageous. We can offer you: Hybrid working Annual discretionary bonus 25 days paid annual leave plus

Regulatory Affairs Senior Specialist - International in London employer: SPD Development Company Ltd

At SPD Swiss Precision Diagnostics, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration in the heart of Bedford. As the Head of Assay, you will not only lead a dynamic team dedicated to developing groundbreaking diagnostic products but also benefit from our commitment to employee growth through tailored coaching, performance management, and a supportive work environment. Join us to make a meaningful impact while enjoying the unique advantages of working within a joint venture that champions scientific excellence and personal development.

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Contact Details:

SPD Development Company Ltd Recruitment Team