Associate Scientist II, Injectable Drug Product Development
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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:
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
You will need to have:
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.
We would prefer for you to have:
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.
Date Posted
23-Oct-2026
Closing Date
22-Oct-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.
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 690 comparable Associate Manufacturing & CMC roles across 100 biopharma companies.
Salary context
156 of 690 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 690 comparable roles
+ 33 more countries
Seniority mix
690 of 690 peers have a known seniority level
Therapeutic area mix
11 of 690 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Open in 3 locations
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.