Moderna is seeking an Associate Director for Analytical Science & Technology (AS&T) at its Norwood, MA site. This leadership role involves overseeing a global team responsible for method validation, transfer strategies, and network data oversight for commercial chemistry and raw material methods. The successful candidate will collaborate cross-functionally to ensure analytical science readiness, consistency, and excellence across the organization.
Lead, mentor, and develop a global team of scientists and specialists, fostering technical excellence and growth.,Build a culture of collaboration, innovation, and continuous improvement.,Lead the design of method validation and transfer strategies for raw material and chemistry methods.,Provide scientific oversight for method robustness, reproducibility, and regulatory alignment across the global network.,Partner with cross-functional teams to design and implement a comprehensive raw material qualification strategy.,Provide strategic oversight for global analytical performance and ensure alignment across sites and partners.,Ensure SOPs, method forms, training documents, and supporting records are complete, compliant, and audit-ready.,Drive holistic implementation and maintenance of documentation and training materials.,Partner with QC leaders to design and oversee training strategies for analyst proficiency.,Provide network-wide data oversight to ensure integrity, consistency, and alignment with global requirements.,Provide expert support in analytical investigations, including method performance issues and raw material testing challenges.,Collaborate with CMOs and suppliers for technical alignment, timely issue resolution, and adherence to company standards.,Act as a key AS&T point of contact for external partners supporting raw materials and chemistry testing.
Advanced degree (MS/PhD) in Chemistry, Analytical Sciences, Pharmaceutical Sciences, or a related field; a BS degree with extensive relevant experience may be considered.,10+ years of relevant experience in pharmaceutical/biotechnology analytical sciences, with direct experience in raw materials and chemistry-focused methods.,Strong expertise in method validation, transfer, lifecycle management, and global regulatory expectations (ICH, USP, Ph. Eur., etc.).,Proven experience leading, mentoring, and developing scientific teams in a global, matrixed environment.,Experience supporting Quality Control (QC) laboratories, training, and investigations in GMP-regulated environments.,Ability to access export-controlled information in accordance with U.S. law; only U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible.
Advanced degree (MS/PhD)
May require occasional travel for site visits, training, or CMO support.,Employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. export control laws. Only U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible. Moderna is unable to sponsor non-U.S. persons for an export control license for this role.,Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Moderna is a biotechnology company pioneering a new class of medicines made of messenger RNA (mRNA). The company's platform builds on continuous advances in basic and applied mRNA science, delivery technology and manufacturing, and has allowed the development of therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases, cardiovascular diseases and autoimmune diseases.
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