provide superior Regulatory services to relevant departments within the company and with external Partners with internal product queries from relevant departments Assisting with external product queries from experience in Regulatory Affairs, preferably in human medicines Demonstrable experience across the product
Audits, Quality Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly and other relevant standard operating procedures. Human Resources Advises QA Manager on requirements for Audits, Quality Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly
Audits, Quality Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly and other relevant standard operating procedures. Human Resources Advises QA Manager on requirements for Audits, Quality Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly
in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable experience across the product
in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable experience across the product
As a pivotal leader in our pricing department, you'll spearhead strategic initiatives, oversee risk professionals, collaborate with cross-functional departments, and shape the direction of our organization's
manage a team of analysts and drive the technical department ensuring that ISO 17025 validations are planned submit, as well as all other functions within the department are followed through and done correctly. Minimum a team of analysts and driving the technical department ensuring that ISO 17025 validations are planned
manage a team of analysts and drive the technical department ensuring that ISO 17025 validations are planned submit, as well as all other functions within the department are followed through and done correctly. Minimum a team of analysts and driving the technical department ensuring that ISO 17025 validations are planned
Associate experience within the regulatory affairs department at a pharmaceutical company to apply. The role tasks. Faxing, filing, liaising with various departments and regulatory bodies, following up with SAHPRA
Associate experience within the regulatory affairs department at a pharmaceutical company to apply. The role tasks. Faxing, filing, liaising with various departments and regulatory bodies, following up with SAHPRA