Assoc. Dir, Project Management

Large molecule method development, validation, and/or transfer experience

Knowledge of deviation management and change control processes

QC Laboratory Due Diligence Experience

Experience with laboratory data management systems (i.e.

Experience with software automation/digital systems (e.g.

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The Global Quality - Large Molecule Analytical Sciences (GQ-LMAS) team leads the global analytical technical oversight of late-stage pipeline programs through commercialization and launch as well as product lifecycle management support for Large Molecules (Vaccines and Biologics), and Cross-Modality Compounds (e.g.

Antibody-Drug Conjugates).

This position will influence life-cycle management of our company’s commercial products and include a specific focus on support of local testing requirements for our company's large molecule commercial products in China.

The position will involve direct contact with government laboratories and functions in China (for example CDE and NIFDC) in addition to Contract Manufacturing and Contract Testing Organizations.

These interactions will include technical discussions and troubleshooting assistance as needed to enable and maintain robust local testing programs in order to ensure uninterrupted supply of our company's biologics and vaccines products in China.

Establish and maintain an excellent professional relationship with scientists working in China's government and contract testing laboratories.