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The Process Engineer III will support downstream tech transfer and manufacturing processes, focusing on late-stage and commercial biologics, documentation creation, and regulatory compliance.

The QA Associate executes day-to-day QA responsibilities in GMP manufacturing, ensuring compliance with cGMPs, reviewing batch records, and supporting audits while collaborating cross-functionally.

The QA Senior Specialist ensures compliance in cGMP operations, trains junior staff, reviews documents, leads audits, and manages quality compliance issues.

The QA Specialist ensures compliance with cGMP in biopharmaceutical manufacturing by reviewing Batch Records, conducting audits, and collaborating with cross-functional teams. Responsibilities include training staff, investigating manufacturing events, and monitoring product quality.

The Process Engineer I will collaborate on projects, develop and execute manufacturing processes for biotherapeutics, ensuring compliance with safety and quality standards.

The Senior Automation Engineer will oversee the AVEVA PI system deployment, integration with process control systems, and ensure data governance in a global manufacturing environment.

The VP of Regional Sales drives sales growth, manages teams, builds client relationships, and develops strategies to meet commercial goals in the life sciences sector.

The Senior Director, Quality Assurance will lead quality strategy for early-phase clinical programs, establishing quality systems and governance according to regulatory standards and ensuring compliance while managing direct reports.

The Senior Scientist Bioassay will conduct QC testing, ensure compliance with GMP, support method development, and mentor junior staff.

As a Process Engineer III, you'll lead technology design, validation, and procurement in manufacturing, optimizing processes and providing operational support while ensuring compliance with regulations.