Continuous Direct Compression Process Engineer - Pharmaceutical Development
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious diseases. Butwe'remore than one of the world's leading pharmaceutical companies. At AstraZeneca,we'reproud to have a unique workplace culture of inclusion and diversity that inspires innovation and collaboration.
Pharmaceutical Technology & Development (PT&D), which employs around 500 people at AstraZeneca Gothenburg, designs and delivers the active drug products (including formulations, devices, and packaging),requiredto support development of new medicines. Likewise, we design and deliver products to be used in toxicology studies or clinical trials, and we develop technology to ensure that a drug product can be scaled up andestablishedat a commercial production site.
AtGlobalProduct Development (GPD)in Gothenburg, a sub-division of PT&D, we focus on the fields of Immediate Release Drug Productsand Oral Controlled Release Drug products. You will join a vibrant team that is working on the next generation ofmedicines and play a key role in the development oftechnology andnew medicinal products.
We are now recruiting a Continuous Direct Compression (CDC)process engineer, to join the Process Technology and Engineering unit, a sub team of GPD.
Whatyou’lldo
We are looking for anengineer/scientistwith the capability and desire to develop further withinthe CDCtechnology area. The rolewill focus on hands-on work with the CDC equipment, along with associateddocumentation.
The role holder will actively contribute to the delivery of products on the CDC line being an expert on CDC technology, and on mechanical operation of the CDC line.You will alsohave the opportunity tobuild and contribute with key data and input into our drug development projects.In this role, it is vital to have a passion for mechanical understanding of the CDC technology, project delivery through CDC technology as well as an interest inidentifyingpossibilities to optimise and maximizethe useof the equipment.
Therolewillinclude:
Being anGPD expert on CDC process in product development,to togetherwith project teams delivering AZ drug project portfolio.
Assemble, run, disassemble, and clean the CDC equipment.
Development,optimisationand implementation ofmanufacturetechnology
Support drug development projects,through knowledge sharingandperformnon-CDC lab work when time allows.
Ensuring that work is performed safely andinaccordance withquality systems.
Progressing work in the most efficient way by being flexible and prioritising the most important activities, and at the same time applying a continuous improvement mindset.
Preparing documentation and formal reportsin accordance withcurrent standards and whereappropriate toGLP (Good Laboratory Practice) and GMP (Good Manufacturing Practice).
Ensure development of high quality and robust drug products and manufacturing processes to support the product control strategy, marketingapplicationsand downstream commercialisation activities, e.g. technology transfer and launch.
Help delivering our project portfolio by engagement, efficiency, high qualityworkand a collaborative spirit.
Supporttechnical transfer to commercial sites
Contributing to project and organisation by a willingness to learn and develop self, but also to support others in their development.
Contribute to andproposeimprovement projects.
Use digital tools, large languagemodelsand development agentsto improve efficiencyand enhance the way we work.
The role may also include:
Generating, assessing, and reporting data with a clear understanding of its reliability, interpreting findings, drawing conclusions and recommendations so that their significance can be appreciated in cross-functional interactions.
Presenting information for discussion at project teams, withinGlobalProduct Development and/or across other functions.
Support to TA projects with formulation development not only related to CDCtechnology and equipment.
Minimumexperience
Educational backgroundwithinengineering; MSc in arelevant engineering disciplineor equivalent qualifications and experience.
Genuine interest in manufacturing technology and to work hands-on with equipment.
Experience from modern engineering tools and digital modelling.
Knowledgeable in and proven experience of using digital tools
At AstraZenecawe’rededicated to being a Great Place to Work where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.
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. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
We look forward to finding out more about you. Welcome with your application no later thanApril12, 2026!
Date Posted
25-mars-2026Closing Date
05-apr.-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.
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