The Position
The Associate Director (Associate Principal Scientist), Organon Manufacturing & Supply (OMS), Chemistry, Manufacturing & Controls (CMC), Network Project & Resource Management will provide regulatory CMC support for Organon Network Projects. This position will lead the preparation and submission of CMC dossiers for assigned Network Projects. The individual may also support project team goals and organizational initiatives on an as-needed basis.
This will include oversight and monitoring of assigned CMC project timelines. This position will work alongside CMC Product Leaders, OMS Network Teams, and CMC partners to ensure progress to achieve project goals. The position will also be responsible for providing CMC support to the Network Project CMC Lead for project strategy.
This position will also be responsible for working with outsourced support of Network activities in alignment with the OMS CMC outsource strategy. This includes proactive collaboration with external partners to monitor, report, and act on delivery performance and quality of deliverables.
The incumbent requires in-depth knowledge and skills in CMC strategy, with strong capability in project management. The successful candidate requires a strong track record of demonstrated knowledge of CMC life cycle management and eCTD.
Responsibilities
Managing processes and connections between external partners and various stakeholders within CMC.
Serves as the CMC Lead for assigned Global Network projects and is accountable for the delivery of all regulatory milestones.
Responsible for overseeing preparation and submission of Global CMC dossiers for assigned Network projects.
Cultivate and foster collaborative relationships with internal and external partners to drive on-time, high-quality delivery of business commitments.
Actively monitor, facilitate, report, and communicate progress against agreed timelines and proactively resolve issues to enable delivery of high-quality, on-time submission information.
Escalate potential delays or performance issues in a timely manner to impacted, cross-functional stakeholders.
Manage communication and change management within the internal organization.
Provide CMC support for Legal Entity Change (LEC) project.
Required Education, Experience and Skills
Bachelor's degree in a science, engineering, or a related field - Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology.
Or Biochemistry - minimum 7 years of relevant experience including biological/pharmaceutical research, manufacturing, testing, or a related field.
Or advanced degree (MS, MBA, Ph.D., PharmD) - minimum 4 years of relevant experience including biological/pharmaceutical research, manufacturing, testing, or a related field.
Strong negotiation, interpersonal, written/oral communication, and fluency in English.
Ability to lead by influence and work effectively in matrix organizational structures.
Project Management.
Good understanding of change management projects.
Preferred Education, Experience and Skills
Degree in pharmacy, biopharmaceutics, analytical chemistry, organic chemistry, chemical engineering, or a related discipline.
Direct experience in Regulatory CMC.
Demonstrated experience driving change initiative projects.
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