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📍 Key Internship Details \n\n • Where Runcorn, UK\n, • Start date January 2027\n, • Duration 9-12 Months \n, • Working model Full-time, on-site \n\n \n 🌱 Grow Your Future at Kerry \n At Kerry, our purpose - Inspiring Food, Nourishing Life - comes to life through science, innovation and sustainable nutrition. From food and beverage to pharma, our teams use insight, technology and science-backed solutions to help solve real-world challenges for people, society and the planet. Our impact reaches billions, but it starts with curious people, fresh ideas and teams who care about making a difference. If you’re looking for a place to learn, contribute and build real experience with purpose, Kerry could be the place for you. \n \n 🚀 Our Internship Programme Your First Step into Kerry \n Our internships give you a real introduction to Kerry - our people, our work and the impact we’re creating through sustainable nutrition. With opportunities across Ireland, the UK and Mainland Europe, you’ll have time to learn, contribute and get a feel for where your career could go next. Demonstrate your potential during your internship and your application for our Graduate Programme will be fast-tracked. \n \n 📊 What You’ll Work On \n As a Research, Development & Application Intern based in Runcorn, you’ll join one of our RD&A teams and gain practical, hands-on experience in our laboratories. Depending on the team you join, your responsibilities may vary, but you’ll support innovation and application projects that contribute to Kerry’s mission of delivering sustainable nutrition. \n\n • Supporting the development of new products and the improvement of existing ones through bench-scale and pilot-scale trials. \n, • Applying scientific principles to help enhance product taste, nutrition and functionality. \n, • Documenting experimental outcomes to support scale-up and product transfer to manufacturing. \n, • Assisting with ingredient and formulation tracking to keep trials consistent and ready to progress. \n, • Maintaining retained samples and checking raw materials are within shelf-life. \n, • Keeping the RD&A lab and equipment organised, operational and ready for project work. \n, • Recording work and time activity using tools such as Salesforce RD&A Tracker. \n, • Taking part in team meetings, training and development activities that help build your technical expertise. \n, • Following Health & Safety protocols in labs, pilot plants and operational areas. \n\n \n 🔎 What We’re Looking For \n You don’t need to have it all figured out. For this internship, we’re looking for someone who is curious, organised and ready to get involved. \n\n • Studying (or recently graduated in) Food Science, Food Technology, Chemistry, Biotechnology, Nutrition, Microbiology, Bioscience, Bakery Technology or a related science degree, and on track for a 21 degree classification. \n, • Curious about how a global business works, and open to learning from the people around you. \n, • Comfortable taking ownership of your work, while knowing when to ask questions or reach out for support. \n, • Eager to explore AI and new technologies, and keen to use them to work smarter, solve real challenges and make a meaningful impact. \n, • Confident using Microsoft Office, including Word, PowerPoint, Excel, Outlook and Teams, and Copilot. \n, • Clear in how you communicate, whether you’re working with your team, sharing updates or managing priorities. \n\n \n 🌟 What’s in It for You \n\n • Annual salary £ 26,227.50 , pro-rated based on the duration of the internship. \n, • See the bigger picture real experience that helps you understand Kerry, our work in sustainable nutrition and how our people bring our purpose to life. \n, • Build your network opportunities to connect with other interns, graduates and colleagues across Kerry. \n, • Share your impact work on a project during your internship and present your contribution at the end of the programme. \n, • Keep growing make a strong impact during your internship, and your application for our Graduate Programme will be fast-tracked. \n\n \n 📝 Ready to Take the First Step? Apply Now! \n If this sounds like the kind of start you’re looking for, we’d love to hear from you. After you apply, candidates who meet the requirements will be invited to complete a psychometric assessment. If successful, you’ll then be invited to a 30-minute virtual interview. \n \n *Please note Applicants must have the right to work full-time in the Country they are applying for.

\n We Are Teva\n We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. How You’ll Spend Your Day\n We are looking for an experienced quality and compliance leader with deep expertise in sterility assurance, microbiology, and contamination control to join our Global Quality organization. In this highly visible global role, you will drive quality, compliance, and operational excellence across Teva's manufacturing network and external partners, supporting inspection readiness, regulatory compliance, modernization initiatives, and contamination prevention strategies. Working closely with Quality, Operations, R&D, Regulatory Affairs, Supply Chain, and Technical Operations teams, you will play a key role in advancing Teva's commitment to product quality and patient safety. \n Travel Requirements: Up to 30% domestic and international travel. \n \n • Define and execute the global sterility assurance (SA) strategy across internal sites and CMOs.\n, • Own aspects of the global microbiology, CCS, aseptic processing, endotoxin control, sterilization, EM, water systems, and CCI governance frameworks.\n, • Lead global policy, standards, and procedural lifecycle management.\n, • Oversee modernization, harmonization, and digitalization efforts.\n, • Serve as primary SME for inspections (FDA, EMA, MHRA), readiness activities, and regulatory responses.\n, • Provide technical support to R&D programs, validation strategies, and regulatory submissions.\n, • Chair cross-functional sterility assurance councils and technical networks.\n, • Manage global risk assessments, mitigation strategies, and contamination/event investigations.\n, • Provide guidance to ensure compliance with Teva's global standards, regulatory guidelines, and cGMP requirements.\n, • Support/lead Global Quality Compliance Initiatives and contribute to Teva's Long Range Plan.\n, • Support critical product incident management events, including complex investigations and CAPA development.\n, • When needed, work collaboratively with the site compliance teams to perform walkthroughs and maturity assessments.\n, • Work with sites to ensure mock audits support a strong state of inspection readiness.\n, • When needed, write or execute protocol for deep dive quality compliance assessments and risk assessments.\n, • Help create, review and monitor the Quality Improvement Plans (QIP) to minimize compliance risk and improve quality performance.\n, • Ensure Quality Risk Management is implemented effectively to assess, control, communicate, and review risks.\n, • Contribute to Teva's Global Compliance Network through GxP interpretation, knowledge sharing, and regulatory guidance.\n Your Skills and Experience\n Do you have? \n \n • Bachelor's degree in Chemistry, Microbiology, Pharmacy, Engineering, or another science-based discipline.\n, • 15+ years of experience in sterile/aseptic pharmaceutical manufacturing, microbiology, quality assurance, or quality compliance roles.\n, • Experience leading in both matrix and functional environments with technical, operational, and people leadership responsibilities.\n, • Extensive experience supporting health authority inspections, regulatory submissions, approvals, and lifecycle management.\n, • Strong knowledge of audit and inspection management, investigations, complaints, and CAPA programs.\n, • Deep aseptic processing expertise, including knowledge of isolators/RABS and Annex 1 requirements.\n, • Experience supporting Environmental Monitoring (EM), Contamination Control Strategies (CCS), and process simulations.\n, • Pharmaceutical quality manufacturing experience within sterile products, biologics, biosimilars, medical devices, or other highly regulated environments.\n, • Strong understanding of cGMP requirements, quality systems, microbiology, quality control, quality assurance, and quality compliance.\n, • Deep knowledge and experience in auditing, compliance, and quality oversight.\n Are You?\n \n, • A recognized subject matter expert who can influence across a global organization.\n, • A strong problem solver with excellent analytical and technical writing skills.\n, • An effective communicator with strong presentation, collaboration, and negotiation skills.\n, • Comfortable operating in a complex, global matrix environment.\n, • Skilled in project management, prioritization, and change leadership.\n, • Proactive, self-motivated, and committed to continuous improvement.\n, • Able to navigate changing priorities while building strong partnerships across functions and cultures.\n How We’ll Take Care of You\n At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. Teva’s Equal Employment Opportunity Commitment\n Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. \n #J-18808-Ljbffr

\n We Are Teva\n We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. How You’ll Spend Your Day\n We are looking for an experienced quality and compliance leader with deep expertise in sterility assurance, microbiology, and contamination control to join our Global Quality organization. In this highly visible global role, you will drive quality, compliance, and operational excellence across Teva's manufacturing network and external partners, supporting inspection readiness, regulatory compliance, modernization initiatives, and contamination prevention strategies. Working closely with Quality, Operations, R&D, Regulatory Affairs, Supply Chain, and Technical Operations teams, you will play a key role in advancing Teva's commitment to product quality and patient safety. \n Travel Requirements: Up to 30% domestic and international travel. Key Responsibilities\n \n • Define and execute the global sterility assurance (SA) strategy across internal sites and CMOs.\n, • Own aspects of the global microbiology, CCS, aseptic processing, endotoxin control, sterilization, EM, water systems, and CCI governance frameworks.\n, • Lead global policy, standards, and procedural lifecycle management.\n, • Oversee modernization, harmonization, and digitalization efforts.\n, • Serve as primary SME for inspections (FDA, EMA, MHRA), readiness activities, and regulatory responses.\n, • Provide technical support to R&D programs, validation strategies, and regulatory submissions.\n, • Chair cross-functional sterility assurance councils and technical networks.\n, • Manage global risk assessments, mitigation strategies, and contamination/event investigations.\n, • Provide guidance to ensure compliance with Teva's global standards, regulatory guidelines, and cGMP requirements.\n, • Support/lead Global Quality Compliance Initiatives and contribute to Teva's Long Range Plan.\n, • Support critical product incident management events, including complex investigations and CAPA development.\n, • When needed, work collaboratively with the site compliance teams to perform walkthroughs and maturity assessments.\n, • Work with sites to ensure mock audits support a strong state of inspection readiness.\n, • When needed, write or execute protocol for deep dive quality compliance assessments and risk assessments.\n, • Help create, review and monitor the Quality Improvement Plans (QIP) to minimize compliance risk and improve quality performance.\n, • Ensure Quality Risk Management is implemented effectively to assess, control, communicate, and review risks.\n, • Contribute to Teva's Global Compliance Network through GxP interpretation, knowledge sharing, and regulatory guidance.\n Your Skills And Experience Do you have?\n \n, • Bachelor's degree in Chemistry, Microbiology, Pharmacy, Engineering, or another science-based discipline.\n, • 15+ years of experience in sterile/aseptic pharmaceutical manufacturing, microbiology, quality assurance, or quality compliance roles.\n, • Experience leading in both matrix and functional environments with technical, operational, and people leadership responsibilities.\n, • Extensive experience supporting health authority inspections, regulatory submissions, approvals, and lifecycle management.\n, • Strong knowledge of audit and inspection management, investigations, complaints, and CAPA programs.\n, • Deep aseptic processing expertise, including knowledge of isolators/RABS and Annex 1 requirements.\n, • Experience supporting Environmental Monitoring (EM), Contamination Control Strategies (CCS), and process simulations.\n, • Pharmaceutical quality manufacturing experience within sterile products, biologics, biosimilars, medical devices, or other highly regulated environments.\n, • Strong understanding of cGMP requirements, quality systems, microbiology, quality control, quality assurance, and quality compliance.\n, • Deep knowledge and experience in auditing, compliance, and quality oversight.\n Are You?\n \n, • A recognized subject matter expert who can influence across a global organization.\n, • A strong problem solver with excellent analytical and technical writing skills.\n, • An effective communicator with strong presentation, collaboration, and negotiation skills.\n, • Comfortable operating in a complex, global matrix environment.\n, • Skilled in project management, prioritization, and change leadership.\n, • Proactive, self-motivated, and committed to continuous improvement.\n, • Able to navigate changing priorities while building strong partnerships across functions and cultures.\n How We’ll Take Care Of You\n At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. \n The deadline for internal applications will be Monday 14th September 2026 Teva’s Equal Employment Opportunity Commitment\n Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. \n #J-18808-Ljbffr

We Are Teva We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. How You'll Spend Your Day We are looking for an experienced quality and compliance leader with deep expertise in sterility assurance, microbiology, and contamination control to join our Global Quality organization. In this highly visible global role, you will drive quality, compliance, and operational excellence across Teva's manufacturing network and external partners, supporting inspection readiness, regulatory compliance, modernization initiatives, and contamination prevention strategies. Working closely with Quality, Operations, R&D, Regulatory Affairs, Supply Chain, and Technical Operations teams, you will play a key role in advancing Teva's commitment to product quality and patient safety. Travel Requirements: Up to 30% domestic and international travel. Key Responsibilities Define and execute the global sterility assurance (SA) strategy across internal sites and CMOs. Own aspects of the global microbiology, CCS, aseptic processing, endotoxin control, sterilization, EM, water systems, and CCI governance frameworks. Lead global policy, standards, and procedural lifecycle management. Oversee modernization, harmonization, and digitalization efforts. Serve as primary SME for inspections (FDA, EMA, MHRA), readiness activities, and regulatory responses. Provide technical support to R&D programs, validation strategies, and regulatory submissions. Chair cross-functional sterility assurance councils and technical networks. Manage global risk assessments, mitigation strategies, and contamination/event investigations. Provide guidance to ensure compliance with Teva's global standards, regulatory guidelines, and cGMP requirements. Support/lead Global Quality Compliance Initiatives and contribute to Teva's Long Range Plan. Support critical product incident management events, including complex investigations and CAPA development. When needed, work collaboratively with the site compliance teams to perform walkthroughs and maturity assessments. Work with sites to ensure mock audits support a strong state of inspection readiness. When needed, write or execute protocol for deep dive quality compliance assessments and risk assessments. Help create, review and monitor the Quality Improvement Plans (QIP) to minimize compliance risk and improve quality performance. Ensure Quality Risk Management is implemented effectively to assess, control, communicate, and review risks. Contribute to Teva's Global Compliance Network through GxP interpretation, knowledge sharing, and regulatory guidance. Your Skills and Experience Do you have? Bachelor's degree in Chemistry, Microbiology, Pharmacy, Engineering, or another science-based discipline. 15+ years of experience in sterile/aseptic pharmaceutical manufacturing, microbiology, quality assurance, or quality compliance roles. Experience leading in both matrix and functional environments with technical, operational, and people leadership responsibilities. Extensive experience supporting health authority inspections, regulatory submissions, approvals, and lifecycle management. Strong knowledge of audit and inspection management, investigations, complaints, and CAPA programs. Deep aseptic processing expertise, including knowledge of isolators/RABS and Annex 1 requirements. Experience supporting Environmental Monitoring (EM), Contamination Control Strategies (CCS), and process simulations. Pharmaceutical quality manufacturing experience within sterile products, biologics, biosimilars, medical devices, or other highly regulated environments. Strong understanding of cGMP requirements, quality systems, microbiology, quality control, quality assurance, and quality compliance. Deep knowledge and experience in auditing, compliance, and quality oversight. Are You? A recognized subject matter expert who can influence across a global organization. A strong problem solver with excellent analytical and technical writing skills. An effective communicator with strong presentation, collaboration, and negotiation skills. Comfortable operating in a complex, global matrix environment. Skilled in project management, prioritization, and change leadership. Proactive, self-motivated, and committed to continuous improvement. Able to navigate changing priorities while building strong partnerships across functions and cultures. How We'll Take Care of You At Teva, better health starts from within, and that includes you. From day one, you'll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you'll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you'll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. Already Working @Teva? Make sure to apply through our internal career site on Twist-your one-stop shop for career development The deadline for internal applications will be Monday 14th September 2026 Teva's Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. TPBN1_UKTJ

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