Principal Engineer, Biologics Drug Substance Technology Transfer

This is what you will do:
The position will lead tech transfer of early and late clinical phase drug substance, to both internal and external contract development & manufacturing (CDMO) companies. Providing scientific leadership, mentorship for junior team members and subject matter expertise for all aspects of drug substance including: technology transfer, process fit analysis, process modelling, raw material controls and aspectic process assurance/microbiological control. The Principal Engineer will also lead timely risk identification, communication and resolution and work in close collaboration with Process Development and Clinical Supply (PDCS), non-GMP internal Pilot network, Alexion Operations, Quality (QA), Regulatory (RA), Analytical Development Quality Control (ADQC) and internal and external Manufacturing sites.
Other areas of responsibility include technical support for ongoing clinical manufacturing, process troubleshooting to manufacturing activities such as supporting process related investigations, deviation resolution, corrective actions/preventative actions, and direct responsibility for process monitoring/control charting of manufacturing operations. Review of technical documents and support for regulatory submissions (IND/IMPD, BLA/MAA) are some other responsibilities. The successful candidate must have mature team-working behaviors and organizational awareness and insight.
You will be responsible for:
Manage and Lead technical transfer process and ensure alignment with CMC schedule to meet program and company goals / metrics, as the need arises. This includes communication with Quality Assurance, Quality Control, Upstream and Downstream Process Development, Drug Product Development, Analytical Sciences and Supply Chain teams to ensure efficient tech transfer of Alexion's clinical drug substance manufacturing activities.
Provide technical leadership and oversight for internal and external technology transfers
Lead technical evaluation and contribute to selection of external manufacturing facilities for drug substance
Perform facility fit analysis, process gap assessments, and establish operational control strategy for each new receiving site
Lead efforts to assess readiness for early and/or late phase transfers using appropriate tools and manage risk communication with leadership along with proposed mitigation/s
Lead creation and/or technical review of batch records, process validation protocols, change controls, and deviations to support GMP manufacturing throughout lifecycle of biologics pipeline in partnering with QA and Alexion operations as applicable
Ensure appropriate data management, perform process monitoring and communicate operation status to management. Provide technical depth and lead OOT and deviation investigations as required
Serve as Drug Substance Team Lead, including representation at CMC asset team, to support late-stage pipeline programs through validation campaigns and initial commercialization, as required
identify issues and risks and lead cross functional team to identify and drive alignment on action/mitigation plan for path forward
Lead continuous improvement of efficiency of technology transfer plans and work process and influence manufacturing sites to focus on improving efficiency of technology transfer processes
ollaboration of all involved functions and external parties
Manage and develop matrix team providing opportunities and actively supporting career enhancement and growth
Co-author and review IND/IMPD, BLA/MAA and other technical documents for regulatory agency submissions
Global role requiring domestic and international travel (~20%)
You will need to have:
PhD in biochemistry, biological science, or chemical engineering or related fields with 6+ years of relevant experience, or BS/MS with 10+years of relevant experience in biopharmaceutical organization with expertise in drug substance development and/or tech transfer
Passport and ability to travel domestically and internationally for manufacturing site support
This role is primarily office based. During travel for manufacturing support, this role requires physical capabilities to gown and don PPE in GMP cleanroom environment and be present during manufacturing operations in a technical support role. Physical elements include standing, climbing stairs, ladders, visual capability to read manufacturing control screens, use a computer, engage in communications via phone, video, and electronic messaging. Intellectual capabilities include engaging in problem solving and non-linear thought, analysis, and dialogue, collaboration with other peer functional representatives.
Requires technical services experience for discrepancy resolution, CAPA implementation and process data monitoring for internal and external facilities
Experience with upstream or downstream manufacturing of monoclonal antibodies/therapeutic proteins with lab and pilot plant operations (non-GMP/GMP)
Requires strong understanding of technology transfer, process fit analysis and clinical phase appropriate process oversight and control, with expertise in late phase technology transfer and validation
Comprehensive understanding of cGMP/ICH requirements for clinical and commercial biopharmaceuticals
Ability to present and defend technical aspects of manufacturing operations during regulatory agency inspections
Ability to influence others without direct authority, including external partners, and connect with all levels of the organization
Strong project leadership and resource management skills along with good verbal and relationship skills
Ability to support development of ambitious and achievable project plans to ensure effective execution
We would prefer for you to have:
Knowledge in planning for program advancement to process validation and commercial launch, with experience supporting teams through BLA approvals
Solid understanding and experience in downstream bioprocess development, scale-up, technology transfer, and process characterization.
Expertise in CFD modeling
Expertise in raw material or microbiological control strategy
Capability to analyze data using basic statistical methods, and present comparability analysis in evidence of effective transfer
Knowledge of quality attribute measurement assays and application to troubleshooting product quality related discrepancies.
Structured problem solving experience
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. Thats why we work, on average, a minimum of four days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.
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.

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