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The Senior Associate Scientist II in Biochemical Analysis will perform laboratory testing, participate in method validation, draft methods, and ensure compliance with cGMP regulations.

The Process Engineer supports operations by optimizing packaging and labeling processes, leading continuous improvement initiatives, and ensuring compliance with GMP standards.

The Scientist I is responsible for method evaluation, optimization, transfer, and validation under cGMP for large molecules and biologics product development, including laboratory testing and documentation.

The role involves executing lab work, maintaining documentation, drafting technical documents, performing technical reviews, and assisting in efficiency projects. Training others and adhering to safety requirements are also key responsibilities.

The EHS Analyst ensures EHS compliance by assessing risks, conducting audits, and collaborating with various departments on environmental, health, and safety initiatives.

The Process Engineer for MS&T supports technology transfer and ensures successful execution of biologic processes, authoring documentation and improving processes for manufacturing operations.

The Project Manager leads CDMO client projects throughout the product lifecycle, ensuring customer satisfaction and compliance with quality standards while managing relationships and project timelines.

The Manager of QA Operations leads a team ensuring compliance with cGMP and QMS requirements, manages client relationships, and drives continuous improvement initiatives.

The Director of Human Resources will manage HR strategy, employee relations, talent development, compensation, and HR operations across multiple sites.

The Senior EHS Specialist ensures regulatory compliance and oversees EHS programs, including audits and investigations to promote employee health and safety.