Associate Director Jobs in Redwood City, Latest Associate Director Jobs in Redwood City

The Associate Director of Quality Systems and Compliance (QSC), reporting to VP of Quality amp; Regulatory, will be responsible for the GxP Quality Systems, ensuring continuous process improvement and compliance to applicable standards and regulations (e.g. ISO 9001, 21 CFR Parts 11, 210, and 211). This role will be responsible for Change Management, Training Program, Documentation Management, Date Integrity, Risk Assessment, Supplier Management, and Audit Program. What You'll Do- Responsible fo

Synthego is enabling genome engineering at scale with a blend of scientific instrumentation, industrial automation, and data science. Our team of scientists and engineers are putting multidisciplinary fields together to solve problems that no one field can tackle alone. We are searching for an experienced and innovative leader to manage our CRISPRevolution operations. With a focus on quality and scale, this role will be responsible for establishing world-class operating protocols. The ideal c

Synthego is looking for an Associate Director of Cost Accounting for our fast-growing and evolving business needs. The Associate Director of Cost will provide significant input into month-end close and budget processes as well as supporting business decision-making and other accounting processes. Their primary responsibilities are to own and lead the cost and inventory functions within the Accounting organization reporting to the VP, Finance amp; Accounting.What You'll Do: - Responsible for all

The Associate Director, Regulatory Affairs, Oncology will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Ensures timely preparation of organized and scientifically valid submissions involving our oncology programs. Provides expertise in translating regulatory requirements into practical, workable plans for project teams with international participants. May mentor and potentially supervise other regulatory profe

The QA Associate Director will work closely with the Development team in Redwood City and the Development QA Team in Copenhagen to support ongoing responsibilities and defined goals by ensuring that activities are in compliance with Ascendis Pharma’s Quality Management System. The QA Associate Director/Director will be responsible for ensuring that development activities are conducted in accordance with EU GMP and US GMP to support the different activities conducted on a global scale. The QA Ass