Associate Scientist II; Injectable Drug Product Development

This Is What You Will Do

Associate Scientist II candidate will be part of the Injectable Drug Product Development (IDPD) team within the Pharmaceutical Development and Clinical Supply (PDCS) department at Alexion-AstraZeneca Rare Disease. The job entails experimental work on various aspects of drug product formulation and process development activities in support of drug product manufacturing, characterization, including analytical and biophysical comparability testing. The ability to work with minimal supervision as well as being part of a collaborative team is essential.

The position entails study design, execution, and preparation of development reports and other required documentation.

• Design and execute formulation and process development studies for clinical biologic candidates with some supervision.
• Execute drug development studies including physico-chemical characterization and stability studies for clinical and commercial drug products.
• Characterize conformational and colloidal stability using industry standard methodology (e.g., circular dichroism, differential scanning fluorimetry, analytical ultracentrifugation, size-exclusion chromatography with multi-angle light scattering detection, etc.).
• Maintain organized records and use team tools to keep multiple assignments on track.
• Assist in the preparation of internal technical reports on executed studies with minimal supervision.
• Participate in cross‑functional development teams.

• BS or MS degree in Biochemistry, Pharmaceutical Science, Chemical Engineering, or relevant field.
• Minimum of 1+ years of relevant work experience with a pharmaceutical or biotechnology company.
• Scientific and practical knowledge of protein/peptide biochemistry, protein formulation, lipid‑based nanoparticle (LNP) development, and stability.
• Experience with imaged capillary electrophoresis (iCE/Maurice), H/UPLC’s (IEX, SEC), DLS, CD, DSC, AUC, and Nano Temper.
• Experience with gene editing product development (mRNA‑based and LNP process development) is highly desirable.
• Ability to execute experiments with minimal supervision.
• Ability to work in a collaborative setting and adhere to timelines.
• Excellent interpersonal, collaborative and communication skills.
• Ability to take initiative in problem solving and finding solutions to scientific challenges.
• Experience with various software packages like MS Office programs (Word, Excel, Outlook, PowerPoint).
• Lab environment duties: ability to lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video and electronic messaging; maintain general availability during standard business hours.

• Hands‑on experience with process development, scale‑up, tech transfer, and manufacturing.
• Experience working with sub‑visible particle testing and characterization.
• Experience with biophysical and analytical testing.
• Familiarity with regulatory guidelines.
• High level proficiency in MS Office software.
• Experience with electronic record‑keeping software (ELN, End Note, e‑logbooks) and maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade).

Date Posted
: 05-Mar-2026

Closing Date
: 18-Mar-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.