Associate Scientist II, Injectable Drug Product Development

AstraZeneca • New Haven, CT

1d • Onsite

About The Position

The Associate Scientist II candidate is encouraged to be a member of the Injectable Drug Product Development (IDPD) team. This team is part of 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 independently 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.

Requirements

• 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 complete experiments independently 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
• 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

Nice To Haves

• 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 (prioritizing PMs, data backup, SW upgrade, etc.) will be a plus.

Responsibilities

• With some supervision, design and implement formulation and process development studies for clinical biologic candidates
• Drive 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 implemented studies with minimal supervision
• Participate in cross-functional development teams

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level