Location: Waterford, Ireland Start date: 1 June 2026 Duration: 3 months Work Model: full-time, On-site About the job As a Product Supply Engineering Summer Student, you will join our engineering team in Waterford and support the improvement of manufacturing processes and equipment performance. This role offers a great opportunity to learn how engineering supports the production of medicines while working alongside experienced professionals. You will contribute to process monitoring, troubleshooting, and continuous improvement initiatives that help ensure safe, efficient, and reliable manufacturing operations. Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you’ll be empowered to learn, ask questions, and bring your ideas to life – all while supported by inspiring mentors and collaborative teams. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main responsibilities Support the team in monitoring manufacturing processes and equipment performance Help investigate process or equipment issues and contribute to problem-solving activities Assist with identifying opportunities to improve efficiency, product quality, and reliability Support qualification activities for new products, processes, or equipment Help review and analyze production and machine performance data Contribute to improvement projects and help track progress against timelines Assist the team with activities related to new product introductions and process improvements About you To excel in this role you will need to have: Currently studying engineering or a related technical field Fluent English (written and spoken) Familiarity with Microsoft tools such as Excel, Word, PowerPoint, or Power BI A curious mindset and interest in understanding how manufacturing processes work Strong problem-solving and analytical thinking skills The ability to collaborate and communicate clearly within a team Attention to detail when supporting documentation and technical tasks Nice to have (not required) Exposure to or interest in manufacturing or production environments Familiarity with 3D design or CAD tools (e.g., SolidWorks, Fusion 360, or similar) Why choose us? Stretch your skills through apprenticeships, internships, graduate programs, and international experiences that grow with you. Learn from inspiring mentors and collaborative teams while contributing to real projects that shape the future of healthcare. Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve. Explore more with personalized development plans, short-term gigs, and internal mobility across functions and countries. Grow in a purpose-driven company where your voice matters and your work helps improve millions of lives. Thrive in inclusive, flexible workplaces that support your personal and professional well-being. Launch your career with a company that invests in you — and empowers you to reimagine what’s possible. #J-18808-Ljbffr
A leading biopharma company located in Waterford, Ireland is seeking a Product Supply Engineering Summer Student to join their engineering team. This role includes supporting manufacturing processes and contributing to improvements in equipment performance. Candidates should be studying engineering and possess strong problem-solving skills along with familiarity with Microsoft tools. The position also offers opportunities for personal and professional growth while working with experienced mentors in a dynamic healthcare environment. #J-18808-Ljbffr
MSAT Visual Inspection Lead Location: Site based from Waterford, Val-De-Reuil, Le Trait, Frankfurt or other Drug Product Site in Sanofi About the job Our Team: We are an R&D-driven, AI-powered biopharma company with one unwavering purpose: to chase the miracles of science and improve people’s lives. Our deep understanding of the immune system—combined with an innovative and growing pipeline—enables us to invent medicines and vaccines that treat and protect millions of people worldwide. At Sanofi, we believe that progress is powered by people: bold thinkers, collaborative leaders, and passionate scientists who dare to push boundaries every day. Join us and help change the world. This is a great opportunity to shape the future of Visual Inspection (VI) on a global scale. As the Global MSAT Visual Inspection Lead, you will be at the heart of Sanofi’s injectable manufacturing excellence—driving the strategy, standardization, and innovation of visual inspection programs across a network of drug product sites in three Global Business Units (GBUs). You will lead a team of VI experts, champion cutting‑edge inspection technologies and processes, and serve as the authoritative voice connecting Manufacturing Science, Analytics & Technology (MSAT) with Global Quality, Engineering, Procurement, and Business Strategy. This is more than a technical leadership role—it is a platform to inspire teams, influence industry practices, and deliver meaningful impact for patients worldwide. Main responsibilities: Lead the Global Visual Inspection program as MSAT authority, serving as a strategic partner in Sanofi’s enterprise‑wide VI strategy while aligning Global Quality, Global Engineering, Procurement, Business Strategy, and injectable manufacturing sites on all VI‑related topics. Build, lead, and develop a high‑performing team of VI experts distributed across 8 sites, providing specialist support across the full Drug Product injectable network. Drive global harmonization of VI strategy and implementation across Manual (MVI), Semi‑Automated (SAVI), and Automated (AVI) inspection modalities for vials, pre‑filled syringes, and cartridges. Deliver expert technical guidance on defect classification, VI recipe optimization, particulate control, false reject rate reduction, robotics, and layered inspection technologies, ensuring holistic VI lifecycle management. Lead the evaluation and acquisition of new VI lines and emerging technologies, ensuring full alignment with quality, regulatory, and operational requirements across the network. Champion innovation and industry benchmarking by identifying cost‑effective inspection solutions and actively engaging with PDA, Biophorum, A3P, and other industry bodies to define and disseminate best practices across the organization. Ensure full regulatory compliance and good documentation practices while providing structured mentorship and knowledge transfer to develop VI capability across new and existing associates. About you Proven background in injectable manufacturing within a cGMP environment, with dedicated expertise in visual inspection and a track record of leadership and impact. Demonstrated experience in transformation programs, technology transfer, validation, and manufacturing support. Qualifications Advanced degree in a scientific discipline. Deep knowledge of GMP, CMC requirements, and current regulatory guidance and best practices in visual inspection, as defined by global health authorities. Experience preparing and reviewing regulatory dossiers with direct health authority interactions. Skills & Competencies Exceptional leadership presence—able to inspire, influence, and align cross‑functional and multicultural teams without direct authority. Outstanding communication skills, with the confidence to engage senior stakeholders and represent Sanofi in external industry forums. Proven ability to operate autonomously in complex, matrixed, and international environments. Operational & Language Fluency in English required; proficiency in an additional European language is a valued asset. Flexibility to provide occasional off‑shift support, remotely or on‑site, as operational needs require. #J-18808-Ljbffr
A leading global biopharma firm is seeking a Global MSAT Visual Inspection Lead. This role involves driving strategy and standardization of visual inspection programs while leading a team of experts across multiple sites. The ideal candidate has a robust background in injectable manufacturing and a strong commitment to regulatory compliance. Exceptional leadership and communication skills are essential, along with fluency in English. Join us to influence industry practices and make a meaningful patient impact. #J-18808-Ljbffr
A leading biopharma company is seeking a Senior Medical Advisor for autoimmune Type 1 Diabetes. This role involves developing medical strategies in the UK and Ireland, collaborating with healthcare professionals, and ensuring that innovative treatments are accessible. The ideal candidate will have a strong background in Medical Affairs and a deep knowledge of Type 1 Diabetes. Opportunities for career growth in a supportive environment are provided, alongside a commitment to improving patient outcomes. #J-18808-Ljbffr
Job Title: (Senior) Medical Advisor, aT1D Location: Reading, UK About This Role As Senior Medical Advisor for autoimmune Type 1 Diabetes (aT1D) within our Medical Affairs team, you'll play a pivotal role in shaping the future of T1D management in the UK and Ireland — leading the local medical strategy, driving cross‑functional alignment, and championing early intervention through innovative, omnichannel approaches that transform patient outcomes. Ready to get started? Join the team transforming how healthcare is delivered for chronic and specialty conditions worldwide. In General Medicines, you'll help drive meaningful outcomes in diabetes, transplant, and immunology - with the scale and urgency patients deserve. About Sanofi We're an R&D‑driven, AI‑powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives. Main Responsibilities Develop and lead the medical strategy for autoimmune Type 1 Diabetes treatments in the UK and Ireland, ensuring our approach aligns with local healthcare needs and global objectives Build strong partnerships with healthcare professionals, patient advocacy groups, and key opinion leaders to advance early detection and intervention in Type 1 Diabetes care Collaborate closely with commercial and market access teams to demonstrate the clinical value of our therapies and support successful product launches Generate and analyze medical evidence by working with research teams, attending scientific conferences, and translating insights into actionable strategies that improve patient outcomes Create engaging educational content and digital tools for healthcare professionals, using multiple communication channels to share the latest scientific developments Ensure all activities meet regulatory standards and ethical guidelines while managing early access programs for patients who could benefit from innovative treatments Represent the UK and Ireland perspective in global clinical development discussions, influencing how new treatments are designed and tested About You You have a strong background in Medical Affairs within the pharmaceutical or healthcare industry, with deep knowledge of Type 1 Diabetes, immunology, or related therapeutic areas. You can develop and execute medical strategies that balance scientific rigor with practical implementation, and you're comfortable navigating ambiguity in a fast‑evolving field. You excel at building trust and collaboration with healthcare professionals, cross‑functional teams, and external stakeholders to achieve shared goals. You can translate complex scientific information into clear, compelling messages for diverse audiences, both in writing and presentations. Fluency in English is essential. Why Choose Us Help shape the future of care for chronic and complex conditions like aT1D, Type 2 diabetes, transplant, and cardiovascular disease. Drive meaningful impact at global scale: our medicines reach more than 100 million people each year. Be part of a simpler, digital‑and‑AI‑powered business that's rethinking how we work and engage with the world. Turn bold ideas into breakthrough launches, with multiple new therapies planned through 2030 and beyond. Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle. Work in a place that combines global scale with local expertise, backed by a strong culture of collaboration and shared purpose. Contribute to innovations that improve outcomes, relieve pressure on healthcare systems, and expand access worldwide. Join a team that's not just transforming treatment - but asking what's next, and making it real. Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice. We are proud to be a Disability Confident Employer, committed to offering interviews to candidates who request consideration under the Scheme and meet the minimum requirements for this role. If you have a disability and require adjustments for the interview process, please email us at diversity.recruitmentUKIE@sanofi.com. We are dedicated to ensuring an inclusive and supportive experience for all applicants. Visas for those who do not already have the right to work in the UK will be considered on a case by case basis according to business needs and resources. Pursue Progress. Discover Extraordinary. Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never‑been‑done‑before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law. #J-18808-Ljbffr
