Title: Project Management Office Reports to: Chief Executive Officer The Project Management Office (PMO) is responsible for driving high complexity, strategic initiatives across the organization. This includes the development of new pharmaceutical products, implementation of innovative technologies, regulatory compliance, and…
The Research and Development (R&D) QA and Technical Documentation Associate Manager is responsible for the compliance to in house and external specifications, standards, guidance such as GMP, SOPs, ICH, Pharmacopoeias, FDA, EMEA, HC and ANVISA required for an R&D centre.…