affairs scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally 2 full years of RA Scioentist or RA Associate experience at a pharma company to apply. Salary is negotiable influenced by your qualifications, your level of experience, and your number of years in a similar role.
need one full year of RA Officer / RA Associate experience within the regulatory affairs department at a position requires a candidate with practical experience as a Regulatory Affairs Scientist / RA Associate least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company to apply. Matric/
need one full year of RA Officer / RA Associate experience within the regulatory affairs department at a position requires a candidate with practical experience as a Regulatory Affairs Scientist / RA Associate least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company to apply. Matric/
in Chemistry (NQF level 7) • Experience: A minimum of 5 years' experience in a laboratory environment workplace environment. • Preferably 3 years' experience in Metal Pre-Treatment and chemical surface preparation ISO 14001 knowledge and practical experience • Knowledge and experience with technical data sheets including pictures of the product. • A minimum of 3 years' experience as a team manager in a Professional leadership
Required minimum work experience: Minimum of 2 years project management experience in a low- or middle-income additional education, work experience, and personal abilities: Experience working within the public health health sector Experience managing a clinical trial Good data management skills Able to work well in a you do meet the minimum job requirements and experience as mentioned above, may you submit a detailed
Required minimum work experience: Minimum of 2 years project management experience in a low- or middle-income additional education, work experience, and personal abilities: Experience working within the public health health sector Experience managing a clinical trial Good data management skills Able to work well in a you do meet the minimum job requirements and experience as mentioned above, may you submit a detailed
minimum work experience:
relevant to PV or pharmacoepidemiology. Extensive experience of PV in the Pharmaceutical Industry, with focus aggregate report writing and risk management. Experience of orphan drug/rare diseases/biologics preferred safety preferred. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency inquiries, and product quality issues. Experience in reviewing different aggregate report types Safety reports, and RMPs is mandatory. Prior experience in supporting business development activities
relevant professional body • At least 5 years of experience as a medical laboratory technologist/ scientist of experience in quality assurance with understanding of Quality Management Program • Experience in Good • Certified Medical Technologist preferred. • Experience in clinical safety laboratory management, PBMC processing, sample storage and clinical trial experience • Understanding of HIV diagnostics testing preferred
relevant professional body • At least 5 years of experience as a medical laboratory technologist/ scientist of experience in quality assurance with understanding of Quality Management Program • Experience in Good • Certified Medical Technologist preferred. • Experience in clinical safety laboratory management, PBMC processing, sample storage and clinical trial experience • Understanding of HIV diagnostics testing preferred