A global healthcare company seeks a Regulatory Affairs professional to guide regulatory processes in the UK. Responsibilities include serving as the primary liaison with the MHRA, managing regulatory submissions, and collaborating with internal and external stakeholders. Ideal candidates will have a degree in Pharmacy or related fields and experience with regulatory strategy development. Join us...
A leading NHS organization in Greater London is seeking a Quality Team Leader for Pharmacy Technical Services. In this role, you will oversee compliance with GMP/GCP standards, manage audits, and enhance the Quality Management System. The successful candidate will provide leadership to a vibrant team, ensuring excellence in service delivery and regulatory adherence. Opportunities for professional...
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed...
You will work across clinical, regulatory, and R&D teams to enable safe and timely access to cutting-edge healthcare solutions.
You will play a key role in shaping regulatory strategy for high-impact clinical technologies, helping bring advanced surgical solutions safely to patients.
Role Overview: Salary : From £50,000 per annum - depending upon experience Hours : 0900 – 1800, weekdays Location : Holborn, London Contract : Opportunity for flexible days/contract based role Role Summary: The CQC Compliance Manager role is an essential part of the Clinic, supporting the Senior Leadership Team, acting as the day-to-day lead for all matters related to the Care Quality...
Qualified Person (QP) – Pharmaceutical Manufacturing & Quality Industry: Global Pharmaceuticals / Life Sciences Location: London, United Kingdom (On-site / Manufacturing & Corporate Quality Office) Type: Full-Time, Permanent Salary Band: £90,000 – £110,000 + Benefits Experience Level: Senior (8–15 Years) The Role (Why This Exists): We are supporting a global pharmaceutical...
You will provide leadership within the research team, collaborate cross-functionally, and maintain the highest standards of participant safety, protocol compliance, and data integrity in complex and sensitive research environments. Key responsibilities include:
The Qualified Person (QP) will be responsible for ensuring that each batch of medicinal product is manufactured and checked in compliance with applicable laws, EU/UK regulations, and Marketing Authorization requirements prior to release. The QP will act as the primary authority for quality, compliance, and batch certification, ensuring patient safety and regulatory adherence across UK/EU...
We’re not just another health communications agency. We’re a multi-expertise collective of strategists, creatives, and problem-solvers - built for clients that refuse to settle. For clients ready to break through today’s complex health challenges, we’re the ones who make it happen. Fast, frictionless, and future-ready, we break down traditional communications siloes, and craft solutions that are...
You will be responsible for: - Driving a positive Quality culture throughout the facility, assisting with continuous improvement activities on site. - Ensuring all manufacturing, testing and release activities are carried out in accordance with current GMP regulations. - Carrying out Qualified Person's batch release responsibilities of the company's various products.
Job Description Location: Shoreditch, London Working Structure: Office based (Thursdays we work from home) Reports to: Head of Growth Salary: £35,000 - £50,000 base + double OTE Who are we? Since cannabis was legalised for medical use in the UK back in 2018, Cantourage UK has been as the forefront of building an ecosystem to service patients and businesses across this rapidly-growing space....
You will play a key role in shaping and delivering our QA/RA talent offering across the UK, supporting clients navigating evolving MHRA standards, EU/UK divergence, AI & SaMD regulations, and tightening global compliance frameworks. Key Responsibilities As an experienced consultant, you will be expected to:
Role Overview: Salary: From £50,000 per annum - depending upon experience Hours: 0900 – 1800, weekdays Location: Holborn, London Contract: Opportunity for flexible days/contract based role Role Summary: The CQC Compliance Manager role is an essential part of the Clinic, supporting the Senior Leadership Team, acting as the day-to-day lead for all matters related to the Care Quality...
You will work across clinical, regulatory, and R&D teams to enable safe and timely access to cutting-edge healthcare solutions.
You will play a key role in shaping regulatory strategy for high-impact clinical technologies, helping bring advanced surgical solutions safely to patients.
You will be responsible for: - Driving a positive Quality culture throughout the facility, assisting with continuous improvement activities on site. - Ensuring all manufacturing, testing and release activities are carried out in accordance with current GMP regulations. - Carrying out Qualified Person's batch release responsibilities of the company's various products.
The Senior Director, Clinical Operations will provide strategic and operational leadership for the planning and execution of global oncology clinical trials, with primary accountability for UK and European clinical operations. This role is responsible for ensuring high-quality, compliant, and efficient trial delivery across multiple programs, working closely with CRO partners and internal...
Job Description The Qualified Person (QP) will be responsible for ensuring that each batch of medicinal product is manufactured and checked in compliance with applicable laws, EU/UK regulations, and Marketing Authorization requirements prior to release. The QP will act as the primary authority for quality, compliance, and batch certification, ensuring patient safety and regulatory adherence...
We’re not just another health communications agency. We’re a multi-expertise collective of strategists, creatives, and problem-solvers - built for clients that refuse to settle. For clients ready to break through today’s complex health challenges, we’re the ones who make it happen. Fast, frictionless, and future-ready, we break down traditional communications siloes, and craft solutions that are...
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed...
You will be responsible for: - Driving a positive Quality culture throughout the facility, assisting with continuous improvement activities on site. - Ensuring all manufacturing, testing and release activities are carried out in accordance with current GMP regulations. - Carrying out Qualified Person's batch release responsibilities of the company's various products.