Regulatory Affairs Team Leader

Paying up to £67,500

High Wycombe (2x days WFH 3x days Office)

Looking to work for a truly fantastic company that looks after their staff and where you are treated as an invividual all whilst working with amazing Medical Device products that are used all over the globe?

Keen to grow and develop in a newly created role where you will manage a team and be invovled in the coaching and developing of staff?

What’s In It for You?:

• Impactful Work: You'll play a critical role in bringing life-changing medical devices to market, ensuring they meet the highest regulatory standards and are backed by robust clinical evidence.
• Professional Development: You'll have access to ongoing training and development programs, including support for certifications and attendance at industry conferences, to keep you at the forefront of regulatory and clinical expertise.
• Innovative Environment: Work alongside a talented, multidisciplinary team in a company that values creativity, innovation, and continuous improvement.
• Work-Life Balance: You will likely be asked to leave at 5pm to go home and enjoy your personal time, this company fosters a fantastic culture where your wellbeing is of utmost importance. 

Here is an insight in what will be your day to day...

• Maintaining Compliance: You will be responsible for managing Medical Device Files to ensure continuous compliance with all relevant regulatory requirements.

• Regulatory Audits: You will prepare for and participate in both internal and external regulatory audits, ensuring the organisation meets all standards.

• Cross-Functional Collaboration: You will provide regulatory and clinical guidance to cross-functional teams, helping to achieve optimal approvals, maintain compliance, and enhance the market potential and lifecycle of products in registered markets.

• Regulatory Interpretation: You will analyse and interpret new regulatory requirements and assess their impact on existing products and markets, ensuring ongoing compliance and strategic adaptation.

What we do need from you...

• At least four years of professional experience in a Regulatory & Clinical setting relating to medical devices, with a high regard for the technical aspects of the functions.
• Have experience of Line Management and task delegation.
• Experience of managing projects and can confidently talk through the project management life cycle.

Want to know more, apply today and let's chat.