Principal Engineer CDC

We have an open position within in our Pharmaceutical Technology and Development (PT&D) department. PT&D is the bridge, which turns brilliant science into actual medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations, and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture. Make a positive impact, in a team where it means more. In Operations, we have a big ambition. to deliver more medicines to patients, quicker and more affordable. Backed by investment, leadership, and a clear plan to get there, we bring personal dedication and out-of-the-box thinking. Summary : As Principal Engineer Continuous Direct Compression (CDC), you will be responsible for coordinating and leading CDC process and equipment design, development and optimisation on late stage oral solid dose drug product development projects. Building predictive tools and digital twins and CDC process development capability to progress the development of oral small molecules within a dynamic team environment will be your key focus. To deliver these goals, you will work and coordinate collaboratively across boundaries with colleagues with diverse scientific expertise e.g. analysts, formulators, engineers, data scientists, materials scientists and other disciplines e.g clinical supply chain, project leadership, regulatory, outsourcing Key Responsibilities : Lead our engineering capability in CDC, to design and develop robust manufacturing processes for new pharmaceutical formulations, ensuring compliance with industry standards. Drive effective technical risk management to ensure that appropriate activities are conducted throughout development to deliver robust commercial manufacture Work effectively with colleagues across Global Product Development, Global Operations and at our external manufacturing partners, to define critical process parameters (CPPs) that influence product quality, in consideration of the wider product control strategy Expedite adoption and advancement of in silico process modelling and control in CDC, and progress our capabilities in advanced process control Lead technology transfer and process validation approaches in CDC Liaise effectively across the AstraZeneca technical and supply network to influence network capability requirements for CDC Work with equipment manufacturers to evaluate and specify technology improvements, in line with AstraZeneca product and portfolio requirements. Provide leadership and coaching to other scientists and engineers within the group, supporting their development to build capability essential to the delivery of the present and future project portfolio. Demonstrate creativity and innovation, driving and supporting a culture of scientific excellence in projects. Stay updated on industry trends, emerging technologies, and best practices in continuous processing to foster innovation within the organization. Essential Requirements: BSc/PhD level education in a relevant Engineering field (Packaging Engineering, Mechanical Engineering, Biomedical Engineering, Materials Engineering, Chemical Engineering), or in Pharmaceutical Sciences with related experience in the device and biopharmaceutical industry is essential. Minimum 5 years relevant experience Industrial experience in pharmaceutical spray drying with a degree in chemical engineering or a closely related scientific discipline. Industrial experience in CDC with a degree in chemical engineering or a closely related scientific discipline. Experience and thorough understanding of oral solid dose drug product development and commercialisation process Proven track record of delivering multiple and/or complex late-stage oral drug product development projects, including technology transfer, scale up and validation of CDC processes Experience of using predictive science / digital tools Experience in development of drug product control strategies, bringing together different aspects of pharmaceutical sciences. Strong collaborative working and communication skills, including ability to work effectively with colleagues from diverse backgrounds and different skill areas. Good organisational and planning skills with the ability to deliver to agreed time and quality. Excellent stakeholder management skills Preferred Skills & Knowledge Experience in development, scale up and technology transfer of a range of other drug product manufacturing processes, eg granulation, tablet compression, coating Experience in clinical and commercial regulatory authoring and defence. Experience of working with external suppliers (such as CMO/CRO for outsourced development and supply) and managing productive relationships. Experience with automation platforms and process modelling When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn't mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Why AstraZeneca: Be part of shaping the future of Operations here at AstraZeneca. Be part of shaping the next phase of Operations' journey towards the 2025 strategy. Build on our foundations of high performance through agility, responsiveness, reliability, and efficiency to deliver our new modalities and complex pipeline to market at speed. Backed by a supportive team, be part of accelerating our operational excellence with innovations in cutting-edge science, Lean ways of working, and fast-changing digital technologies. The annual base pay for this position ranges from $175,572-$263,358 Annual USD. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Date Posted 13-Jan-2026 Closing Date 29-Jan-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.