Associate Scientist IV, Injectable Drug Product Development

This is what you will do:

The Associate Scientist IV will join Injectable Drug Product Development group to support the formulation and drug product process development of Alexion’s biotherapeutic candidates. This individual will develop injectable formulations with fit for purpose analytical methods, perform analytical testing, and draft reports for the executed studies. This individual will work independently in a dynamic team environment and routinely collaborate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply.

You will be responsible for:

• Execution of formulation screening and stability studies for injectable drug products including proteins, oligonucleotides, and peptides.
• Supporting analytical method development and optimization
• Supporting development and tech transfer of GMP fill finish processes to internal and external manufacturing organizations.
• Writing internal technical reports on the executed studies
• Assisting in preparation of external regulatory submissions (IND, BLA etc.) for the Alexion product candidates
• Participate in department meetings and other technical and team building activities

You will need to have:

• BS or MS degree in Biochemistry, Chemistry, Chemical Engineering or related discipline from an accredited university with 6+ years of experience for MS or 7+ years of experience with BS.
• Extensive experience on developing phase appropriate formulations and fill finish processes.
• Working experience on various injectable dosage forms in vials, prefilled syringes/ cartridges.
• Comprehensive understanding of chemistry and stability, and degradation mechanism of proteins and peptides.
• Ability to work in a collaborative setting and adhere to timelines.
• Demonstrated ability to work effectively in a cross-functional settings.
• Firsthand experience with liquid chromatography methods (e.g., SEC, IEX, HIC) and capillary methods (e.g., iCE, LabChip GXII Touch).
• Strong knowledge of analytical software (e.g., Empower, JMP).
• Ability to interpret raw data, organize results and communicate findings to project team and management
• The duties of this role are conducted in an 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 multiple detectors (e.g. UV, FLR, RI, MALS, CAD).
• Excellent interpersonal and communication skills.
• Understanding of the biotechnology products life cycle and factors impacting product stability.
• Knowledge of cGMP and quality guidelines.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.