Regulatory Affairs - London, England

We're looking for a Regulatory Affairs Consultant to help us shape and deliver our regulatory strategy across the Group. · Maintaining positive and transparent relationships with the PRA and FCA, ensuring senior managers are prepared for regulatory meetings and interviews · Coord ...

We are looking for a Regulatory Affairs Consultant to help us shape and deliver our regulatory strategy across the Group. Joining us means helping to improve the lives of our customers and contributing to the success of the business every day. · Strong knowledge of the PRA Rulebo ...

We're looking for a Regulatory Affairs Consultant to help us shape and deliver our regulatory strategy across the Group.In this role you'll collaborate with colleagues at all levels and play a key part in maintaining transparent constructive relationships with our regulators. · ...

We're looking for a Regulatory Affairs Consultant to help us shape and deliver our regulatory strategy across the Group. · ...

Job summaryWe are looking for a RegulatoryAffairs Consultant to help us shape and deliver our regulatory strategyacross the Group. · Strong knowledgeof the PRA Rulebook,FCA Handbook and related regulatory materials · ...

This is a part-time position as Regulatory Affairs Consultant. The consultant will oversee regulatory compliance processes and manage regulatory submissions. · ...

The Regulatory Affairs Manager will play a fundamental role in maintaining continued regulatory compliance with standards and medical device regulations. · Coordinate and manage regulatory submissions and approvals in line with industry standards. · Ensure compliance with applica ...

+As Regulatory Affairs Specialist, you will play a key hands-on role in ensuring our devices meet global regulatory requirements as we prepare for pivotal trials, CA/CE marking, and European launch. · Solid working knowledge of global device regulatory pathways (CE/EU MDR, UKCA, ...

+Support the rollout and ongoing adoption of Veeva RIM within a global pharmaceutical organisation. · +Develop, adapt, and maintain Veeva RIM training materials · Coordinate and deliver training to Super Users and End Users via Up4Growth · ++18 months contract + 40 hours per wee ...

The Regulatory Affairs Analyst will facilitate strong regulatory risk management and ensure a good understanding of regulatory risks, issues, and projects across Pension Insurance Corporation.We achieve our purpose by setting companywide strategic objectives and driving a healthy ...

The Regulatory Affairs Manager plays a key role in the design, development and delivery of an effective strategy that supports jurisdictional regulatory adoption and consistent application of IFRS Standards. · ...

As part of our next phase of growth, we are seeking an experienced Regulatory Affairs Specialist to join the business as a partner. · We are looking for someone who has strong experience in Regulatory Affairs within healthcare, · a strong entrepreneurial mindset and is excited by ...

My global FinTech client is looking for a permanent Regulatory Affairs Analyst to join the team. This is hybrid working – 2-3 days a week in the London office (the first month will be 4 days a week). Paying £40,000 to £60,000 + benefits. · ...

This newly created role offers the opportunity to shape compliance processes for innovative beauty products globally. · Work with raw material suppliers to collect and verify technical documents for compliance. · ...

We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organisation dedicated to advancing clinical research and transforming lives. · ...

The Regulatory Affairs team are the owners of PIC's regulatory strategy including being responsible for managing the relationships with the relevant UK regulators (PRA and FCA). · ...

We are looking for a Regulatory Affairs Manager to play a fundamental role in maintaining our continued regulatory compliance with standards and medical device regulations. · Lead the planning, preparation and submission of new products for multiple regulatory filings; · Manage a ...

· Overview · The Regulatory Affairs Manager will assist in establishing and maintaining quality management systems and will work to ensure all members of the organization are aware of the quality system. This position will work to support the employee compliance with all interna ...

Job summary As part of our next phase of growth, we are seeking an experienced Regulatory Affairs Specialist to join the business as a partner... · ...

The Director, Regulatory Affairs is responsible for developing and implementing regulatory strategies, ensuring alignment with Sr. Management to secure and maintain approval/s for the assigned country and / or region from clinical development through to product approval and comme ...