Associate Principal Scientist, Analytical R&D

Job DescriptionThe Associate Principal Scientist position will support our Live Virus Vaccines (LVV)  franchise.  This broad role includes 1) working with Analytical Product Leaders (APLs) to develop and implement analytical strategies, with special focus on transition from clinical to commercial stages; 2) driving method alignment and supporting consistent executional excellence across multiple testing laboratories; 3) developing and maintaining a robust assay monitoring effort and  supporting method procedure life cycle management, including automation and/or modernization as applicable. This position is technical in nature and demonstrated expertise in vaccine analytics is required.The role also requires effective collaboration with external contract providers as well as colleagues in our research laboratories, supply chain, site and global Quality, as well as CMC-Regulatory.This role will be based in West Point, PA and it’s a site-based position.Responsibilities include but are not limited to:Work with APLs to develop and implement the commercialization analytical strategy across testing nodes.Participate in significant investigations across the viral vaccines franchise.Provide Subject Method Expertise to QC analysts and supervisors, assess impact  of proposed changes and deviations.In partnership with the AWG and network QC labs, support definition of the opportunities for improvement/investment in equipment and technology required to drive assay modernization and implement harmonized network solutions.  This includes working with our Digital manufacturing Division and LMAS team for assay digitization with harmonized data capture.In partnership with the BCR hub, develop short and mid-term strategy for sustainability in BCR inventory and antisera generation needed to support all testing laboratories in the network and connect BCR performance with assay performance as noted above.Provide SME support to APLC gap assessments of key methods to drive improved and sustainable robustness.Ensure method performance data are presented, discussed and actions developed at analytical working group meetings as appropriate.Collaborate across the internal network, external partners, international governments and/or contract manufacturing and research organizations (CMO/CRO) to ensure uninterrupted supplyEscalate key assay challenges to management in a timely and concise manner.Support RTQs, PAI readiness and audit observations Minimum ​Education Requirement and Experience:Bachelor’s Degree (BA/BS) with a concentration in sciences with six (6) years of experience working in the field of analytical testing, development, transfer, and/or validation; ORMaster’s Degree (MA/MS) with a concentration in sciences with four (4) years of experience working in the field of analytical testing, development, transfer, and/or validation; ORPhD with a concentration in sciences with two (2) years of experience working in the field of analytical testing, development, transfer, and/or validation. Required Experience and Skills:Demonstrated experience with analytics for commercial vaccine and/or microbiological products.Effective communication and teamwork. Experience with large molecule GMP testing, including drug substance and drug product stability and release testing.Experience with analytical comparability.Experience leading a cross-functional team.Strong technical expertise in general large molecule analytical laboratory operations, equipment, and techniques. Preferred Experience and Skills:Continuous improvement or Project Management training.Writing or review of technical documents, preferably including regulatory filings (IND, MAA, BLA, PAS, CBE) and inspections with multiple agencies (FDA, EMA, JNDA).Experience with large molecule analytical transfers.Experience with commercial product analytical method changes.Experience with assay monitoring and trending.VETJOBS#eligableforerpRequired Skills: Adaptability, Analytical Method Development, Assay Development, Biological Assay Development, Cell-Based Assays, Chromatographic Techniques, Cross-Functional Teamwork, External Collaboration, High Resolution Mass Spectrometry (HRMS), Liquid Chromatography-Mass Spectrometry (LC-MS), Mass Spectrometry Analysis, Optimism, Process Analytical Technology (PAT), Protein Analysis, TeamworkPreferred Skills: Current Employees apply HERECurrent Contingent Workers apply HEREUS and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your RightsEEOC GINA Supplement​We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State ActsThe salary range for this role is$142,400.00 - $224,100.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of thi