What are the responsibilities and job description for the Associate Scientist II, Injectable Drug Product Development position at Alexion Pharmaceuticals, Inc.?
This Is What You Will Do
The Associate Scientist II candidate will be a 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 part of a collaborative team is essential. The position entails study design, execution, and preparation of development reports and other required documentation.
You Will Be Responsible For
22-Oct-2026
Closing Date
04-Nov-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.
The Associate Scientist II candidate will be a 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 part of a collaborative team is essential. The position entails study design, execution, and preparation of development reports and other required documentation.
You Will Be Responsible For
- With some supervision, design and execute formulation and process development studies for clinical biologic candidates
- 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 with 2 to 4 years relevant work experience with a pharmaceutical or biotechnology company
- Scientific and practical knowledge of protein/peptide biochemistry, protein formulation, and stability is essential.
- Experience of working with imaged capillary electrophoresis (iCE/Maurice), H/UPLC’s (IEX, SEC), DLS, CD, DSC, AUC, and NanoTemper
- Ability to execute experiments with minimal supervision is required. The individual must be able to work in a collaborative setting and has ability to adhere to timelines is essential.
- 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, including Word, Excel, Outlook, and PowerPoint·
- The duties of this role are generally conducted in a lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video and electronic messaging; engage in problem solving and non-linear thought, analysis and dialogue; collaborate with others; 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 of working with biophysical and analytical testing·
- Familiarity with regulatory guidelines.
- High level proficiency in MS Office software including: Word, Excel, Outlook, and PowerPoint.
- Experience with electronic record keeping software, like ELN, EndNote, e-logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) will be a plus.
22-Oct-2026
Closing Date
04-Nov-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.