Associate Principal Scientist, Regulatory Chemistry Manufacturing

h3Job Description /h3 h3The Position /h3 pReporting to the Director or Executive Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and implementing Regulatory Chemistry, Manufacturing Controls (CMC) strategies for assigned small molecule or biological products in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC dossiers for life-cycle maintenance submissions, original registrations, and post-approval changes. The incumbent may manage a team of 1 to 2 individual contributors and/or outsourcing partners in support of project execution. The Associate Principal Scientist may also support project team goals and organizational initiatives, on an as needed basis. /p h3Responsibilities /h3 ul liServe as the CMC Product Lead for assigned products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle. /li liLead development and execution of global product and project regulatory strategy(ies) by ensuring robust assessment of CMC changes, identification of global regulatory requirements and critical evaluation of supporting documentation to confirm acceptability and identification of potential risks. /li liExecute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements, annual reports, registration renewals and responses to health authority questions per established business processes and systems. /li liProvide regulatory leadership as needed to product in-license/due diligence review, product divestment and product withdrawal. /li liCollaborate with Organon Manufacturing Supply colleagues and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. /li liManage execution of CMC documentation including post-approval supplements, annual reports, registration renewals and responses to health authority questions per established business processes and systems. /li liDemonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the company to ensure approval and Product supply continuity. /li liAssess and communicate potential regulatory risks and propose mitigation strategies. /li liDeliver all regulatory milestones for assigned products across the product lifecycle. /li liIdentify, communicate and elevate potential regulatory issues to Organon Regulatory CMC management, as needed. /li /ul h3Required Education, Experience And Skills /h3 ul liBachelor’s degree, in a science, engineering, or a related field. Fields of study include Pharmacy, Chemistry, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry with at least 7 years of relevant experience including biological/pharmaceutical research, manufacturing, testing or a related field OR /li liAdvanced degree (MS, MBA, Ph.
D., PharmD) with at least 4 years of relevant experience including biological/pharmaceutical research, manufacturing, testing or a related field. /li liThe candidate must be proficient in English; additional language skills are a plus. /li liProven experience in critically reviewing detailed scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. /li liDemonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strong listening skills. /li liDemonstrated sound understanding of related fields (e.g., manufacturing, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving. /li liDemonstrated ability to generateinnovative solutions to complex regulatory problems and effectively work with and communicate to key stakeholders. /li liDemonstrated flexibility in responding to changing priorities or dealing with unexpected events. /li liDemonstrated effective leadership, communication, interpersonal and negotiating skills. /li liAbility to lead a team of direct or matrixed colleagues to deliver on business commitments and project timelines. /li /ul h3Preferred Experience And Skills /h3 ul liA candidate with experience in Regulatory CMC post-approval lifecycle management is preferred. /li /ul p#OCMC /p h3Who We Are: /h3 pOrganon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women’s Health,