Advanced GMP Material Scientist with data and AI process responsibility

Job description

Advanced GMP Material Scientist CMC Development CMC Drug Substance Process Operations Location: Bagsværd, Denmark Your impact begins here - Turn science, data and AI into smarter GMP material decisions Are you ready to take ownership of GMP materials across our clinical pipeline while shaping smarter ways of working? Join us at the intersection of science, quality, data and AI, where you will turn complex material requirements and improvement ideas into practical solutions that strengthen compliance, availability and efficiency. If you are ready to make a tangible impact, we would like to hear from you. Join our team as our new Advanced GMP Material Scientist in Chemistry, manufacturing & Control (CMC) Drug Substance Process Operations. Apply today. What you’ll do As Advanced GMP Material Scientist, you will act as Material Responsible for GMP materials used across Novo's clinical pipeline. You will support material qualification and set the right level of incoming control based on material criticality, supplier and supply chain risks, process needs, storage conditions and clinical phase of use. Most importantly, you will become the team’s driving force for data-driven and AI-assisted process optimisations, bringing existing and new ideas to life so materials are fit for purpose, compliant and available when needed. You will take ownership for GMP materials and help the team improve how work gets done. Overall, your work will include: Acting as Material Responsible for GMP materials used within clinical development by supporting material qualification and defining the right level of incoming control. Data-driven and AI-assisted process optimisations within the team and department, turning existing and new ideas into practical improvements. Coordinating across CMC projects and multiple stakeholders, creating clarity and momentum where priorities shift. What you’ll bring We are looking for a quality-minded scientist or engineer who combines scientific curiosity with structure, ownership and collaboration. You hold a relevant MSc (or PhD) within natural science, computer science, pharmacy, engineering or a related field. You will thrive in this role if you have: Experience with, or a strong eagerness to learn about, GMP, QMS and regulated pharmaceutical development or manufacturing. Experience with data-driven and AI-assisted optimizations and related project management in a scientific context. The confidence to set direction, ask questions, challenge assumptions and speak up when something is unclear or stalled. Experience coordinating tasks across projects with many stakeholders and changing priorities. A structured, proactive and collaborative approach to decision-making and follow-through. Equally, strong external experience is valued - what matters most is your ability to learn quickly, collaborate, take ownership and apply sound scientific and quality judgement. Who you’ll work with You will join the GMP Materials team within the CMC Drug Substance Process Operations department, part of the wider CMC Drug Development area in Global Manufacturing & Supply. Based in Bagsværd, the team connects scientific understanding, GMP compliance, supplier knowledge, QMS requirements, supply chain robustness, system data and practical manufacturing needs across Novo's clinical pipeline. You will work closely with CMC projects, QA, QC, sourcing, warehousing and supply chain colleagues, as well as external suppliers. It is a diverse team in personality, culture and professional background, and a team that is highly motivated to implement new strategic initiatives and process optimisations using data and AI platforms, in line with the direction set through The Novo Way. What you can expect here You will work in a collaborative, quality-focused environment where your expertise shapes decisions and your ideas can move things forward. You will be trusted to take ownership, speak up and challenge assumptions, while being supported to grow – whether by deepening your GMP and QMS knowledge or by building new skills at the forefront of data and AI within pharmaceutical development and manufacturing. Salary: For this role, the Annual Base Salary ranges from DKK 570,200 to 838,100, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience. Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks. Learn more about our Reward Philosophy here . Start now Your impact begins today - apply before 21 October 2026. Due to a short deadline, we encourage you to apply as soon as possible. For questions, please contact Sr. manager, Julie Novod Goldenbaum on +45/ 3079 1860. While not mandatory, we strongly encourage you to include a few lines in your CV explaining why this role is the right next step for you. Please refrain from adding a photo to your CV to ensure fair and efficient processing. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.