×
Register Here to Apply for Jobs or Post Jobs. X

Associate Scientist II; Injectable Drug Product Development

Job in New Haven, New Haven County, Connecticut, 06540, USA
Listing for: AstraZeneca GmbH
Full Time position
Listed on 2026-03-10
Job specializations:
  • Healthcare
  • Research/Development
    Research Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Associate Scientist II (Injectable Drug Product Development)

What You Will Do

The 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 compatibility 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.

Responsibilities
  • With some supervision, design and execute formulation and process development studies for clinical biologic candidates.
  • Execute drug development studies including physicochemical 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.
Requirements
  • 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 are essential.
  • Experience working with imaged capillary electrophoresis (iCE/Maurice), H/UPLC (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 is required.
  • The individual must be able 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, 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/de‑gown 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.
Preferred Qualifications
  • Hands‑on experience with process development, scale‑up, tech transfer, and manufacturing.
  • Experience working with sub‑visible particle testing and characterization.
  • Experience 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, End Note, e‑logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) will be a plus.

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.

#J-18808-Ljbffr
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary