Technology Regulatory Lead

system technology ideas for Infrastructure, Mobile, Automotive, and Embedded We are looking for a high-energy, motivated leader to help drive team leader to work alongside technologists, system architects and project and program managers to lead the planning and delivery of technology across multiple initiatives and provide a high quality of service...

ARA-P3-12 Job Title: Regulatory Affairs & Systems Data Manager Location: Cambridge (Hybrid/Flexible) Job type: permanent At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. The Manager will be...

Head of Quality and Regulatory Affairs A fast growing healthcare technology company is looking for a highly skilled and motivated Head of Quality and Regulatory Affairs to join their team. This individual will play a critical role in guiding the organisation's innovative medical products through the regulatory approval process, ensuring compliance with...

Head of Quality and Regulatory Affairs A fast growing healthcare technology company is looking for a highly skilled and motivated Head of Quality and Regulatory Affairs to join their team. This individual will play a critical role in guiding the organisation's innovative medical products through the regulatory approval process, ensuring compliance with...

The Head (Senior Director) International CMC Regulatory Affairs reports to the Executive Director, International Regulatory Strategy and is accountable for leading a team of regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy, delivery, and execution of international CMC Regulatory strategy...

Job Title: Senior Director, Regulatory Affairs Job Type: Full-time, permanent position Cambridge, UK – Hybrid Cpl Life Sciences is collaborating with a prestigious global drug development consultancy business that specialises in supporting pharma, biotechs, spin-outs, and academic groups with drug development activities. The business has a specific...

Job Title: Senior Director, Regulatory Affairs Job Type: Full-time, permanent position Location: Cambridge, UK – Hybrid Remuneration: £130,000 + Benefits Cpl Life Sciences is collaborating with a prestigious global drug development consultancy business that specialises in supporting pharma, biotechs, spin-outs, and academic groups with drug...

Job Title: Senior Director, Regulatory Affairs Job Type: Full-time, permanent position Location: Cambridge, UK – Hybrid Remuneration: £130,000 + Benefits Cpl Life Sciences is collaborating with a prestigious global drug development consultancy business that specialises in supporting pharma, biotechs, spin-outs, and academic groups with drug...

Head of Quality and Regulatory AffairsA fast growing healthcare technology company is looking for a highly skilled and motivated Head of Quality and Regulatory Affairs to join their team. This individual will play a critical role in guiding the organisation's innovative medical products through the regulatory approval process, ensuring compliance with global...

Head of Quality and Regulatory Affairs A fast growing healthcare technology company is looking for a highly skilled and motivated Head of Quality and Regulatory Affairs to join their team. This individual will play a critical role in guiding the organisation's innovative medical products through the regulatory approval process, ensuring compliance with...

Arm has a great opportunity for a Package Design Engineer in our System-in- You will work closely with IP, SoC Design, Package Design, SignalPower Integrity and Systems teams throughout the company as well was interact with leading worldwide technology partners. ecosystems, packaging is a space where innovation is flourishing. xD and 3D approaches are...

This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. Company Description Bicycle Therapeutics is a clinical-stage pharmaceutical company developing a novel class of medicines, referred to as Bicycle molecules, for diseases that are underserved by existing therapeutics. Bicycle molecules are fully synthetic...

Job Purpose As an Associate Director, Regulatory Affairs, you are an integral part of MoonLake’s team and will be responsible for developing and delivering innovative global regulatory strategies for sonelokimab lead indication(s). You will be responsible for regulatory aspects related to product development and approval, in alignment with the global...

Regulatory Compliance SpecialistA renowned healthcare technology company is seeking a highly motivated Regulatory Affairs Manager to lead their regulatory compliance efforts across international markets. This individual will play a critical role in guiding the organization's innovative medical products through the regulatory approval process, ensuring...

The Commercial and Regulatory Affairs Lead will serve as a key figure in navigating the landscape of regulatory compliance for medical technologies, thereby enabling successful research, development, and commercialisation of innovative healthcare solutions from inception to implementation for academic, clinical and SME stakeholders. This role requires an...

The Head (Senior Director) International CMC Regulatory Affairs reports to the Executive Director, International Regulatory Strategy and is accountable for leading a team of regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy, delivery, and execution of international CMC Regulatory strategy...

We are looking for a hardworking, creative person for our Performance Analysis performance measurements and alike - our engineers are part of crafting the This position is in the PPA team (power, performance, area) in Cambridge. measure the performance and energy efficiency in various use cases and analyse the performance to improve the products to...

Estimated salary: £80,000 - £100,000 per annum.About Clinical Professionals LimitedWe are a leading provider of pharmaceutical and biotechnology expertise, supporting the translation of science into medicinal products. Our team is passionate about delivering high-quality services that meet the needs of our clients.Job DescriptionAs an Associate Director,...

Vivify Talent Overview:We're a small yet ambitious regulatory writing consultancy looking for a talented Principal Medical Writer to drive our projects forward. With a focus on flexibility and work-life balance, we offer a unique opportunity to excel in a fully remote role.As a key member of our team, you'll be responsible for leading the creation of...

Regulatory LeadershipVectura Group, a global leader in inhaled therapies and drug-device combination products, seeks a seasoned Regulatory Affairs Manager to drive the success of our medical device and DDCP regulatory activities.Regulatory Expertise: Lead regulatory activities across Vectura Group, specializing in medical devices and DDCPs, to support...