At a Glance
- Tasks: Lead the design and optimisation of pharmaceutical manufacturing processes for innovative drug products.
- Company: Join AstraZeneca, a leader in transforming science into life-changing medicines.
- Benefits: Competitive salary, global collaboration, and opportunities for professional growth.
- Other info: Be part of a diverse team that values innovation, sustainability, and collaboration.
- Why this job: Make a real impact on patient care by developing cutting-edge pharmaceutical processes.
- Qualifications: PhD or MSc in relevant fields with hands-on lab experience in pharmaceutical development.
The predicted salary is between 54000 - 66000 £ per year.
Location: Macclesfield
Salary: Competitive
Introduction to role: Are you ready to turn cutting-edge science into dependable, scalable manufacturing that delivers medicines to patients sooner? Do you thrive at the bench and at the whiteboard, pairing experiments with models to make confident, high-impact decisions? Based in the UK, Macclesfield you will be a laboratory-based senior scientist who combines hands‑on experimentation with modelling, simulation and digital tools to create robust processes for oral and parenteral drug products in late‑stage development. You will join a cross‑functional process technology and engineering team that sits at the interface of science and manufacturing. Here, your work will strengthen process understanding, shape development strategies and influence how new medicines are made at commercial scale. Can you see yourself designing critical experiments in the morning and using digital insights in the afternoon to steer the next wave of development?
Accountabilities:
- Process Design and Optimization: Lead the design, development and optimisation of robust manufacturing processes for oral and parenteral drug products, ensuring long‑term performance and patient needs are met.
- Experimental Process Understanding: Design, execute and interpret laboratory studies to build deep process understanding and generate decision‑enabling data.
- Scale-Up and Technology Transfer: Contribute within cross‑functional teams to develop, scale and transfer reliable commercial manufacturing processes for oral solid dosage forms and parenteral products.
- Modelling and Simulation: Apply modelling, simulation and digital tools to guide experimental strategy, quantify risk and accelerate development timelines.
- Digital Enablement: Champion and advance digital approaches that enhance pharmaceutical process development and strengthen data integrity and reuse.
- Data‑Driven Collaboration: Build strong partnerships with formulation scientists, engineers, modelling and simulation specialists, and manufacturing experts to solve complex technical challenges.
- Technical Planning and Delivery: Independently plan and deliver technical activities to agreed timelines and quality standards, applying sound engineering judgement to interpret results and adapt strategies.
- Scientific Networking and Foresight: Contribute to scientific and technology networks, maintaining awareness of emerging methods and technologies relevant to pharmaceutical product development.
Essential Skills/Experience:
- PhD in Chemical Engineering, Applied Physics or a related scientific discipline, or an MSc with significant industrial experience in pharmaceutical process development.
- Hands‑on laboratory experience, including experimental design, data generation and interpretation to support process understanding and development.
- Demonstrated experience in pharmaceutical process development within CMC, including the design, development and optimisation of drug product manufacturing processes for oral solid dosage forms and/or parenteral products.
- Strong understanding of CMC regulatory requirements, with experience preparing regulatory documentation to support clinical development and/or marketing applications.
- Experience applying modelling, simulation and digital technologies to support process understanding, development and decision‑making.
- Strong scientific problem‑solving skills, with the ability to analyse data, interpret results, and make sound technical decisions.
- Strong collaboration and communication skills, with the ability to work effectively across multidisciplinary teams.
- Ability to work effectively in a global, cross‑functional environment and build strong collaborative relationships across disciplines.
- Excellent written and spoken English.
Desirable Skills/Experience:
- Experience leading engineering work packages, process development activities or technology transfer projects within pharmaceutical development.
- Experience of commercial process development and technology transfer for new chemical entities.
- Experience of continuous processing in a pharmaceutical environment.
- Knowledge of GMP Process Safety and Data Integrity and Change Control requirements.
- Experience working with automated manufacturing systems and digitalised process development environments.
- Experience working with CDMOs and outsourced development activities.
- Experience exploring or applying AI‑enabled tools within pharmaceutical development.
Why AstraZeneca: Join a community where scientists, engineers and digital specialists work side by side to move molecules to medicines with pace and precision. You will influence how a diverse pipeline is developed and manufactured, from high‑tech labs to modern production lines that apply lean thinking, automation and advanced analytics. Here, unexpected combinations of expertise come together to test bold ideas, learn fast and scale what works, all within a culture that values kindness alongside ambition. With strong investment, global reach and a clear focus on sustainability including ambitious goals to cut our environmental footprint, you will build skills for the future while contributing directly to therapies that change lives.
Date Posted: 21‑Oct‑2026
Closing Date: 01‑Nov‑2026
Our 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.
Senior Scientist Process Engineer - Pharmaceutical Product Development employer: AstraZeneca Plc
AstraZeneca is an exceptional employer that fosters a culture of collaboration and innovation, making it an ideal place for a Study Monitor Support Specialist. With a commitment to employee growth through lifelong learning opportunities and a flexible work environment, you will be empowered to contribute to groundbreaking medical advancements while enjoying a supportive team atmosphere. Located in a vibrant area, AstraZeneca offers the chance to work alongside passionate professionals dedicated to making a meaningful impact in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Scientist Process Engineer - Pharmaceutical Product Development
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We think you need these skills to ace Senior Scientist Process Engineer - Pharmaceutical Product Development
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at AstraZeneca Plc!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show AstraZeneca Plc that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at AstraZeneca Plc!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At AstraZeneca Plc, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at AstraZeneca Plc
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at AstraZeneca Plc that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with AstraZeneca Plc’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.