Reference: CT004363-SM-1 JOB SUMMARY Responsible to ensure that regulatory submissions and compliance are executed for all products. Develop and communicate with head office on the regulatory strategy and life cycle management of all products. Represent our company with the local authority and other
products made from human plasma is seeking a Regulatory Affairs Pharmacist who will be responsible to put of regulatory resources in a timely manner Regulatory affairs administration Update the paper and electronic
products made from human plasma is seeking a Regulatory Affairs Pharmacist who will be responsible to put of regulatory resources in a timely manner Regulatory affairs administration Update the paper and electronic
management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for collaboration across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions experience of working in several groups in regulatory affairs or experience at a health authority Knowledge
Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory submission of new products Formulate or implement regulatory affairs systems, policies and procedures to ensure Council Minimum of 5 years' experience in Regulatory Affairs, preferably in human medicines. Demonstrated
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
experience of working in several groups in regulatory affairs or experience at a health authority Knowledge management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for collaboration across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions
opportunity for an experienced regulatory affairs scientist, or senior regulatory affairs associate, to assist experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory affairs scientist scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally, you should similar level to a pharmacist. Assist the regulatory affairs pharmacist team with all aspects of their
An established leader in the pharmaceutical sector has an opportunity for an RA Pharmacist with at least 2 to 4 years of solid RA dossier compilation experience. Experience using Extedo, or docuBridge, or a similar electronic dossier compiling platform is preferred. Experience in RA for CAMS / Compl
A long-established leader in the pharmaceutical sector has an opportunity for an RA Manager to lead their team of RA pharmacists and RA scientists - about 4 to 8 people in the team. The position requires no dossier compilation from you - you will strategically manage the team and ensure output. You