Roche
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. Thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry ten years in a row by the Dow Jones Sustainability Indices (DJSI).
Open roles at Roche
2 roles
License to Operate (LTO) Graduate Rotation Programme
Roche
Welwyn, UK
Roche’s License to Operate graduate programme offers rotations across quality, patient safety, regulatory affairs, clinical operations and medical information to support compliant pharmaceutical operations.The PositionWe aspire to be a leading edge License to Operate (LTO) organisation that drives compliance, quality, and innovative patient-centric solutions, utilising cross-functional expertise across Roche UK to support delivering on our mission and business operations. We strive to create a workplace where team members own their development and learning and are empowered to create and innovate.The OpportunityThis is an excellent opportunity for an individual who has recently graduated with a science background. The role is a rotational programme with the opportunity to work across five sections within the Roche UK License to Operate (LTO) department: Quality, Patient Safety, Regulatory, Medical Clinical Operations, and Medical Information. The programme will run for 2 years, allowing you to spend time in multiple sections to drive cross-functional improvement. Expected start date of the programme is January 2027.Background of each LTO SectionQuality: Responsible for the administration and operational management of key GxP Quality Management System (QMS) processes and supporting the Local Quality Responsible (LQR) and Qualified Persons (QP) to fulfill company and legal obligations.Regulatory: Translates the constantly evolving requirements of the UK Regulatory environment into Roche policies, procedures, solutions, and strategies that ensure compliance and maximize value for patients.Patient Safety: Ensures safety information is collected and recorded accurately to a high standard, actively partnering with the business across activities such as Non-Interventional Studies (NIS), digital activities, market research, and patient support programmes.Medical Clinical Operations (MCO): Provides clinical operations expertise in managing funded interventional and non-interventional studies, managed non-interventional studies, and pre-approval access programs, working across the business and externally with trial sites.Medical Information: Contributes to the safe and effective use of Roche medicines by responding to scientific, technical, and medical enquiries from healthcare professionals (HCPs), patients, and members of the public.Who you are:Applicants should have a recent science degree of 2:1 or above and a strong desire to engage and drive cross-functional improvement.To be successful in this opportunity, applicants should also have:Excellent computer & digital skillsAbility to work reliably and flexiblyStrong communication and analytical skillsAbility to work independently and within a team, developing effective working relationships with a wide range of colleagues
Posted today
Featured
PDR Early Talent Graduate Program
Roche
Welwyn, UK
Roche’s Product Development Regulatory Early Talent Programme builds regulatory affairs skills through pharmaceutical projects, regulatory documentation and collaboration with global drug development teams.The OpportunityEmbark on a transformative two-year journey with the One Product Development Regulatory (PDR) Early Talent (ET) Program, meticulously crafted to impart comprehensive foundational knowledge in regulatory affairs. This dynamic initiative blends hands-on assignments with tailored learning solutions, making it an ideal entry-point for aspiring regulatory professionals. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging in diverse activities across various therapeutic areas and stages of development. The latter part of the program offers the opportunity to rotate into another function or specialize further in PDR.Throughout the program, ETs collaborate with global drug development teams to support the introduction of novel pharmaceutical products to patients worldwide. This environment not only enhances their scientific writing skills but also deepens their understanding of regulatory frameworks by preparing a wide array of regulatory documents and supporting Health Authority Interactions. By joining the One PDR ET Program, participants become pivotal contributors to the regulatory landscape, dedicated to ensuring that life-changing medicines reach those who need them most.Through this opportunity you will:Actively build foundational regulatory experience through your work on regulatory projects with the appropriate mentorship.Take ownership of your own learning and development, actively seeking to understand drug development and regulatory roles, and engaging in knowledge sharing and peer support.Become responsible for understanding and applying business processes to deliver foundational regulatory deliverables.Engage with regulatory and cross functional teams through active listening, practicing open communication, and building trust with global team members.Grasp the vision of the Roche organization, understanding how your work impacts the team and contributes to overall goals.Improve prioritization and time management skills while spending significant time on-site at the Roche office.Who you are:You hold a degree (B.Sc., M.Sc., or Doctorate) in a life sciences, biological sciences, biology, chemistry, Pharmacy, or related field before the start of the program, and you are within two years of completion of a degree program in the before mentioned disciplines.You have no more than 1-year of relevant past pharmaceutical experience post last degree.You have a basic understanding of drug development and entry level understanding of the role of a regulatory professional.You demonstrate a learning mentality, are engaged in personal growth, and actively seek and act on feedback.You foster partnership, collaboration, empowerment, and autonomy to build a strong community.
Posted today
License to Operate (LTO) Graduate Rotation Programme
Roche
Welwyn, UK
Roche’s License to Operate graduate programme offers rotations across quality, patient safety, regulatory affairs, clinical operations and medical information to support compliant pharmaceutical operations.The PositionWe aspire to be a leading edge License to Operate (LTO) organisation that drives compliance, quality, and innovative patient-centric solutions, utilising cross-functional expertise across Roche UK to support delivering on our mission and business operations. We strive to create a workplace where team members own their development and learning and are empowered to create and innovate.The OpportunityThis is an excellent opportunity for an individual who has recently graduated with a science background. The role is a rotational programme with the opportunity to work across five sections within the Roche UK License to Operate (LTO) department: Quality, Patient Safety, Regulatory, Medical Clinical Operations, and Medical Information. The programme will run for 2 years, allowing you to spend time in multiple sections to drive cross-functional improvement. Expected start date of the programme is January 2027.Background of each LTO SectionQuality: Responsible for the administration and operational management of key GxP Quality Management System (QMS) processes and supporting the Local Quality Responsible (LQR) and Qualified Persons (QP) to fulfill company and legal obligations.Regulatory: Translates the constantly evolving requirements of the UK Regulatory environment into Roche policies, procedures, solutions, and strategies that ensure compliance and maximize value for patients.Patient Safety: Ensures safety information is collected and recorded accurately to a high standard, actively partnering with the business across activities such as Non-Interventional Studies (NIS), digital activities, market research, and patient support programmes.Medical Clinical Operations (MCO): Provides clinical operations expertise in managing funded interventional and non-interventional studies, managed non-interventional studies, and pre-approval access programs, working across the business and externally with trial sites.Medical Information: Contributes to the safe and effective use of Roche medicines by responding to scientific, technical, and medical enquiries from healthcare professionals (HCPs), patients, and members of the public.Who you are:Applicants should have a recent science degree of 2:1 or above and a strong desire to engage and drive cross-functional improvement.To be successful in this opportunity, applicants should also have:Excellent computer & digital skillsAbility to work reliably and flexiblyStrong communication and analytical skillsAbility to work independently and within a team, developing effective working relationships with a wide range of colleagues
Posted today
Featured
PDR Early Talent Graduate Program
Roche
Welwyn, UK
Roche’s Product Development Regulatory Early Talent Programme builds regulatory affairs skills through pharmaceutical projects, regulatory documentation and collaboration with global drug development teams.The OpportunityEmbark on a transformative two-year journey with the One Product Development Regulatory (PDR) Early Talent (ET) Program, meticulously crafted to impart comprehensive foundational knowledge in regulatory affairs. This dynamic initiative blends hands-on assignments with tailored learning solutions, making it an ideal entry-point for aspiring regulatory professionals. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging in diverse activities across various therapeutic areas and stages of development. The latter part of the program offers the opportunity to rotate into another function or specialize further in PDR.Throughout the program, ETs collaborate with global drug development teams to support the introduction of novel pharmaceutical products to patients worldwide. This environment not only enhances their scientific writing skills but also deepens their understanding of regulatory frameworks by preparing a wide array of regulatory documents and supporting Health Authority Interactions. By joining the One PDR ET Program, participants become pivotal contributors to the regulatory landscape, dedicated to ensuring that life-changing medicines reach those who need them most.Through this opportunity you will:Actively build foundational regulatory experience through your work on regulatory projects with the appropriate mentorship.Take ownership of your own learning and development, actively seeking to understand drug development and regulatory roles, and engaging in knowledge sharing and peer support.Become responsible for understanding and applying business processes to deliver foundational regulatory deliverables.Engage with regulatory and cross functional teams through active listening, practicing open communication, and building trust with global team members.Grasp the vision of the Roche organization, understanding how your work impacts the team and contributes to overall goals.Improve prioritization and time management skills while spending significant time on-site at the Roche office.Who you are:You hold a degree (B.Sc., M.Sc., or Doctorate) in a life sciences, biological sciences, biology, chemistry, Pharmacy, or related field before the start of the program, and you are within two years of completion of a degree program in the before mentioned disciplines.You have no more than 1-year of relevant past pharmaceutical experience post last degree.You have a basic understanding of drug development and entry level understanding of the role of a regulatory professional.You demonstrate a learning mentality, are engaged in personal growth, and actively seek and act on feedback.You foster partnership, collaboration, empowerment, and autonomy to build a strong community.
Posted today
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