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The Senior Scientist performs complex sample preparations and analyses, coordinates lab activities, manages QC responsibilities, and leads study design and evaluation.

The Manager of Regulatory Affairs - CMC will prepare CMC packages for submissions and manage global change control assessments while ensuring compliance with regulations. They will provide regulatory strategy advice and lead project teams, ensuring high-quality standards and alignment with clients for effective project management.

Manage and lead EHS programs, ensuring compliance with safety regulations, conducting training, and collaborating with teams to improve practices.

Oversee the EMEA Returnable Drum Program, drive strategy, manage product lifecycle, collaborate with teams, and ensure customer satisfaction through effective management and reporting.

The Credit Controller Representative I will manage customer accounts, ensure compliance with terms, perform risk assessments, support collections, and provide financial statement analysis.

The Regulatory Affairs Specialist I will manage compliance processes, collaborate with teams on product planning, evaluate suppliers, monitor regulatory changes, and conduct risk assessments to support product development and acquisitions.

The role involves authoring regulatory submissions, collaborating with departments, and managing compliance in CMC for biotech products.

The Research Scientist conducts method development, validates projects, interprets data, leads troubleshooting, prepares reports, and mentors others in an innovative laboratory environment.

The Technical Writer creates user documentation for scientific products by collaborating with product teams, organizing content, and managing multiple writing projects.

Manage the Technical Communications team, ensuring high-quality user documentation. Train writers, prioritize projects, and improve documentation through feedback and analytics.