This is what you will do:

The Associate Scientist II will join Injectable Drug Product Development group to support the development of Alexion’s bio-therapeutic candidates. Design and drive experiments to develop injectable drug product formulations and process characterization studies, including analyzing samples and authoring technical reports. Join a dynamic and collaborative team with multi-functional business partners within Product Development and Clinical Supply.

You will be responsible for:

Execution of formulation screening and stability studies for injectable drug products including proteins, siRNAs, peptidesImplement supporting analytical methods and analysis for samplesSupporting process development and tech transfer of GMP fill finish processes to internal and external manufacturing organizationsDefining drug product processes, scale up studies, transferring information between development and manufacturing sites, as well as preparation of required tech transfer documentKnowledge of cGMP and quality guidelines is requiredWriting internal technical reports on the performed studiesAssisting in preparation of external regulatory submissions for the Alexion product candidatesParticipate in department meetings and other technical and team building activities

You will need to have:

Hands-on experience on developing phase appropriate drug product formulations and fill finish processesBasic principles of protein chemistry and stability, and biologic therapeutic degradation mechanismsAbility implement and deliver timelinesHands-on experience with liquid chromatography methods (e.g., SEC, IEX, HIC) and capillary methods (e.g. iCE, LabChip GXII Touch)Experience with analytical software (e.g. Empower, JMP) and electronic record keeping software, like (ELN)The duties of this role are generally conducted in a lab environment. As is typical of a lab-based role, employees are required, 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, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours

We would prefer for you to have:

BS or MS degree in Biochemistry, Chemistry, Chemical Engineering or related field with 1+ years of experience for MS or 2+ years of experience with BSExcellent interpersonal and Partnership ability!Understanding of the biotechnology products life cycle and factors impacting product stability.High level proficiency in MS Office software including Word, Excel, Outlook, and PowerPoint

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.