Development Scientist I, Analytical Development and Quality Control
AstraZeneca

This is what you will do:

The Development Scientist I position is a technical position responsible for development and optimization of release and stability methods including physicochemical methods pertaining to Imaged Capillary Electrophoresis (icIEF) as well as traditional Gel/Capillary Electrophoresis (CE-SDS, CIEF, CZE, IEF and SDS-PAGE) as well as support for chromatography charge separation (IEX) for clinical and commercial biotherapeutics. This position will also support other analytical method development related to characterization and investigation efforts, as well as conduct testing for Alexion's biotherapeutic products when required. Participation in method validation and transfer or troubleshooting of methods to internal and external laboratories may be required. In addition, this position is expected to interact regularly with scientific staff in other Research & Development groups as well as Manufacturing, Quality Assurance and Quality Control groups.

You will be responsible for:

• Development, optimization, and phase-appropriate qualification of custom capillary electrophoresis methods to evaluate key quality attributes for therapeutic proteins (charge heterogeneity, primary structure, PTMs, size variant, etc.)
• Organizing activities of self and others as well as supervise operation, maintenance and troubleshooting of analytical instrumentation (e.g., Revvity LabChip, Protein Simple iCE3 and MauriCE)
• Supporting application of new innovative technologies to improve throughput and enhance capability of cGMP testing
• Authoring SOPs, study plans, protocols, and method development reports. Draft reports for regulatory filing
• Working with various Research and Development teams to support transfer of analytical test methods for development and clinical support.
• Collaborating with Analytical Technical Transfer Services (ATTS) to develop and execute validation protocols, provide support during and post method transfer (e.g. on-site training and troubleshooting as needed)
• Maintaining knowledge of current scientific principles and theories. Train other lab personnel as assigned in areas of expertise and participate in cross-functional process development teams
• Seeking out and evaluate new instruments, methods, techniques, and technology platforms to enhance analytical operations

You will need to have:

• Ph.D. degree or master's degree with equivalent level of experience, in Chemistry, Biochemistry, Chemical Engineering or related discipline.
• Analytical method development experience in protein/peptide analysis by gel/capillary electrophoresis in pharmaceutical or biotechnology company is a plus.
• Scientific and practical knowledge of protein characterization for protein therapeutics including monoclonal antibodies and glycoproteins.
• Experience with assay development, optimization, qualification, and validation for protein therapeutics is a significant plus.
• Ability to take initiative in problem solving and consistently bring independent, scientific approach to method development.
• Knowledge of cGMP and quality guidelines is desired.
• Ability to travel up to 20% to support on-site training and troubleshooting.
• The duties of this role are 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:

• Experience with assay development, optimization, qualification, and validation for protein therapeutics.
• Excellent people skills and a strong ability to communicate effectively.
• Knowledge of cGMP and quality guidelines (e.g., ICH Q2 and ICH Q14)
• High level of proficiency in MS Office software including Word, Excel, Outlook, Visio, and PowerPoint
• The ability to accurately and independently contribute and oversee the generation of procedures, protocols and reports pertaining to test methods.
• The ability to manage and lead projects independently, drive CE method development strategies, improve quality and efficiency of workflows, provide scientific guidance to team members, and train and oversee some day-to-day responsibilities of junior scientists.
• Ability to lead and participate in cross-functional development teams representing Analytical Development and Quality Control.
• Experience with authoring and reviewing CMC sections for regulatory, technical reports, department specific protocols and reports and generating operating procedures is a significant plus.

Expectation of working in the office 4 days a week statement: When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

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.

This job has expired.