Role Description Are you ready to embark on an exciting journey as a Cellular Therapies Quality Lead at GenesisCare UK? Join our dedicated team and be part of something extraordinary. This newly created national role offers a unique opportunity to help shape the future of cellular therapy services within a leading independent cancer care provider. As our cellular therapies programme continues to grow, we are establishing a dedicated quality leadership role to strengthen governance, regulatory compliance and service excellence across the entire pathway. As the Cellular Therapies Quality Lead with us, you'll play a pivotal role in providing expert leadership and oversight of the quality management system across cellular therapy services. Working closely with clinical, operational and laboratory teams, you will ensure compliance with national accreditation standards including JACIE, CQC and related regulatory frameworks, while promoting a culture of safety, learning and continuous improvement. This is your opportunity to make a meaningful impact, helping to embed high-quality systems and processes across the end-to-end cellular therapies pathway while supporting the continued development of these innovative treatment services within GenesisCare. Qualifications - Experience managing Quality Management Systems within regulated healthcare environments. - Strong understanding of JACIE, HTA, CQC or similar accreditation frameworks. - Experience supporting regulatory inspections and accreditation readiness. - Experience delivering internal audits and managing quality improvement actions. - Knowledge of incident investigation, risk management and clinical governance processes. - Strong analytical skills with the ability to interpret and present complex quality data. - Excellent communication and influencing skills when working with multidisciplinary teams. - Degree-level education in a scientific, clinical or quality-related discipline (or equivalent experience). - Postgraduate training in quality management or regulatory compliance (desirable). - Ability to work independently while collaborating effectively across teams. Requirements - Lead and maintain the Quality Management System (QMS) for cellular therapy services, ensuring regulatory compliance. - Coordinate regulatory and accreditation inspections, including preparation, staff readiness and post-inspection action planning. - Oversee controlled documentation, ensuring robust review processes, traceability and version control. - Deliver and manage an internal audit programme, identifying improvement opportunities and ensuring effective action implementation. - Support governance across the cellular therapies pathway including incident management, risk oversight and performance monitoring. - Provide specialist advice on regulatory and accreditation standards across the service. - Maintain training and competency frameworks, ensuring staff meet regulatory and procedural requirements. - Analyse and present quality and performance data to support assurance and informed decision-making. - Collaborate with clinical, operational and laboratory teams to ensure alignment across the cellular therapy pathway. - Promote a culture of continuous improvement, safety and high-quality patient care. Benefits - Shape your work-life balance with 26 days of annual leave, plus bank holidays, and the option to buy more or sell back annual leave. - Prioritise your well-being with complimentary private medical and dental coverage, access to Employee Assistance Program, and Income Protection. - Access our world-class radiotherapy – free to you and your immediate family, if required. - Secure your future with a competitive Company Contributory Pension Scheme. - Nurture your mental health and well-being through our well-being community, with access to Babylon Health and Headspace Wellbeing. - Enjoy hassle-free commutes with free parking at most of our centres. - Treat yourself with exclusive retail discounts. Company Description GenesisCare UK is the leading provider of private oncology services in the UK, pioneering a transformation in cancer care. Through innovative, personalised treatments, we are enhancing patient quality of life, life expectancy, and overall survival rates. We are a team of over 600 highly trained physicians, healthcare professionals and support staff operating 14 specialist outpatient cancer centres across the UK. Our aim is to provide world-class care, offering the latest proven treatments including advanced diagnostics, medical oncology, radiotherapy and Theranostics. We take an integrated approach to cancer care, focusing on treating the whole patient, not just the cancer. Our personalised treatment programmes include wellbeing services in partnership with Penny Brohn UK and exercise medicine, proven to enhance patient outcomes. Collaborating with universities and leading clinicians globally, we're dedicated to researching and developing improved cancer treatments. Our UK clinical trials programme aims to broaden access to new therapies. We’re passionate about innovation and working together to make great things happen. We make significant investments in our employees to provide opportunities for growth, learning, and development within their roles. Join GenesisCare UK and shape your future, while shaping the future of cancer care.

• Provide comprehensive technical support and expertise in risk-based quality management of clinical trials • Oversee internal and external compliance with ICH E6 (R3), organizational procedures, and applicable regulatory standards • Support the Marburg Vaccine (cAd3-Marburg) and Sudan Virus Vaccine (cAd3-Sudan) development activities • Promote a quality culture within the organization • Partner with Clinical Operations, CROs, and clinical sites to provide GXP CQA oversight • Develop risk-based clinical quality sponsor oversight initiatives • Plan and conduct audits of CROs, clinical sites, and documentation, ensuring compliance with policies and regulations • Author audit reports and oversee findings until resolution, including implementation of any CAPAs through effectiveness checks • Participate in internal and external audits/inspections including other quality assurance assigned activities • Assist in development and implementation of sponsor oversight and quality systems to identify trends and noncompliance • Manage, create and review CQA SOP’s and documentation as required • Assist in development and implementation of quality systems to identify, initiate and monitor corrective and preventive actions.

• Review copy to ensure adherence to style guide and content guidelines for design system components, patterns, and templates. • Flag subjective wording, phrasing, or grammar choices (that aren't definitive style guide violations) and collaborates with content designer if further copyediting is needed. • Identify patterns that have issues related to consistency across content landscape. • Run automated (AI-driven) reports to compare content in design files with content in staging environment. • Review reports and collaborate with content designers to ensure report is fully valid. • Identify refinements or improvements to style guide to improve automated reports. • Participate in governance meetings. • Act as backup to Copy Editor, helping with proofreading content in Drupal CMS before publishing. • Support additional reporting needs, such as pulling data analytics and customer feedback scores and compiling reports. • Other responsibilities as assigned.

Role Description As the Marketing Quality Specialist, you will play a critical role in ensuring the quality and accuracy of our marketing materials and campaigns. This position requires extensive experience in quality assurance, exceptional leadership skills, and a deep understanding of marketing. You will guide and support the team to ensure all content meets the highest standards of quality and aligns with our client’s brand guidelines and the industry’s expectations. What You'll Do - Subject Matter Expert: Provide expert guidance and support to the team, ensuring that all marketing materials meet the highest quality standards. - Quality Assurance: Conduct thorough reviews of marketing materials, including content, graphics, and advertisements, to ensure accuracy, consistency, and adherence to brand guidelines. - Proofreading: Proofread all marketing content for grammatical, typographical, and factual errors, ensuring flawless and polished deliverables. - Campaign Review: Collaborate with the marketing team to review and approve marketing campaigns, ensuring they meet quality standards and align with strategic objectives. - Process Improvement: Develop and implement quality assurance processes and checklists to streamline and enhance the review process for marketing materials while also providing visibility for leadership. - Feedback and Training: Provide constructive feedback to team members and conduct training sessions to improve overall quality and consistency in marketing outputs. - Collaboration: Work closely with designers, content creators, and marketing managers to ensure seamless communication and alignment on quality standards. Qualifications - Bachelor's degree in Marketing, Communications, English, or a related field. - 5+ years of experience in quality assurance within a marketing department or agency. - Exceptional attention to detail and strong proofreading skills. - Excellent written and verbal communication skills. - Proven experience in leading and managing a team. - Ability to manage multiple tasks and prioritize effectively in a fast-paced environment. - Proficiency with quality assurance tools and processes. - Strong interpersonal skills and the ability to work collaboratively with cross-functional teams. - A proactive approach to identifying and addressing quality issues. Benefits - Competitive salary - Comprehensive benefits package (401k Match, Cigna for health, vision, dental, PTO, Paid Holidays, Corporate Equipment). - Outstanding collaborative work environment. - Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position. - Compensation Range: $50,000 - $60,000. - We are not sponsoring visas for this role at this time.