Formulation Senior Scientist

At AstraZeneca, we transform ideas into life-changing medicines and are dedicated to meeting the unmet needs of patients worldwide. Working here means embracing scientific curiosity, being hands-on in problem-solving, and collaborating effectively to achieve innovative results. If you hold an advanced degree related to formulation science, with excellent communication and collaboration skills, experience in product development, and the ability to combine hands-on lab work with digital tools, you’ll thrive with us.

AstraZeneca is a global, science-driven biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines and healthcare solutions that enrich patients' lives. 

One vision of our global Pharmaceutical Sciences function is to deliver the therapies of the future through scientific leadership in drug delivery. Our portfolio includes projects ranging from traditional small molecules to nucleotide-based therapies and nanomedicines across AstraZeneca’s therapy areas.

The formulation development teams in Early Product Development & Manufacturing (EPDM) focus on developing small molecules into oral drug products for our drug projects. We are responsible for progressing candidate compounds from the pre-clinical phase up to phase 2b clinical studies.  

This is a unique opportunity for an enthusiastic, innovative, and motivated Formulation Scientist to join our formulation development team in EPDM at AstraZeneca’s R&D site in Gothenburg, Sweden. Join us and become part of a dedicated team, working on drug delivery of various drug molecules in close collaboration with other experts to drive our drug projects forward.

What You’ll Do 

This is an exciting role where you will act as member of project teams, providing technical and scientific expertise in formulation design and development strategies. You will develop and deliver oral solid dosage forms for phase I and phase II clinical studies. You will work in an environment that blends hands-on formulation with digital, predictive and automated approaches. 

Close collaboration with internal skill groups and external partners will be essential to develop the drug product, alongside engaging with customers to develop solutions from a broader perspective. As a member of cross‑functional project teams, the role operates with a high degree of independence, representing the group and area of expertise. Responsibility includes defining lead formulations to deliver the desired clinical performance, with significant contributions to CMC (Chemistry, Manufacturing, and Control) aspects and deliverables.

Lab‑based experimental work will be conducted according to project timelines, integrating predictive and digital tools throughout development. Work will be documented in line with current standards and, where appropriate, GMP, while also contributing to CMC regulatory submissions.

Outsourcing of formulation development and manufacturing to external partners may also be part of this role. You may further develop your expertise by developing new technologies and processes, or through involvement in science & technology initiatives.

Essential for the Role 

• Degree (MSc or PhD) in a discipline relevant to formulation science, chemical engineering, pharmaceutical technology, or equivalent qualifications. 

• Experience in formulation development, or related product development area. 

• Genuine interest in experimental work and hands-on problem solving. 

• Experience of applying modelling and simulation tools. 

• Delivery-focused with the ability to utilize scientific and innovative thinking.  

• Strong communication and collaboration skills. 

• Excellent English, both written and spoken. 

Desirable for the Role 

• Technical competence in oral solid drug product development, preferably with industry experience. 

• Experience delivering Phase I/II oral solid dosage clinical supplies under GMP and transferring processes to clinical manufacturing. 

• Experience in partnering with CDMOs/CROs 

• Ability to drive science and author scientific publications and/or CMC regulatory documentation. 

• Good understanding of appropriate quality standards and regulatory frameworks. 

If your passion is turning science into medicines and you want to be part of a team that makes a significant impact on patients’ lives, there’s no better place to be. 

So, What’s Next? 

Are you already imagining yourself joining our team, apply now!  We look forward to receiving your application (CV and cover letter) no later than May 17th, 2026. Please combine your cover letter and CV into a single document before uploading. 

Date Posted

24-Apr-2026

Closing Date

17-May-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.