Head of Regulatory Affairs (POS24078) R 1,8mill per annum Based in Midrand BEE Candidates only to apply Job Purpose: The Head of Regulatory Affairs holds
NACOSA is looking for a suitably qualified candidate to fill the position of Grants Manager to have overall responsibility for administration, programme
Required Learning Bachelor's degree in Pharmacy.Registered with the South African Pharmacy Council as a Pharmacist.Minimum of 5 years of experience in
Description General :Aid and support the Responsible Pharmacist to ensure compliance to:SAHPRA for compliance with the requirements of the Medicines and
Job Location Rivonia-Johannesburg Job Description General : Aid and support the Responsible Pharmacist to ensure compliance to: SAHPRA for compliance with the
Main purpose of the job: To implement pharmaceutical services as per GPP and protocols for clinical research studies at Wits RHI Location: 22 Esselen Street,
Main purpose of the job:To implement pharmaceutical services as per GPP and protocols for clinical research studies at Wits RHILocation:22 Esselen Street,
Main purpose of the job:To implement pharmaceutical services as per GPP and protocols for clinical research studies at Wits RHILocation:22 Esselen Street,
Main purpose of the job:To implement pharmaceutical services as per GPP and protocols for clinical research studies at Wits RHILocation:22 Esselen Street,
Main purpose of the job:To implement pharmaceutical services as per GPP and protocols for clinical research studies at Wits RHILocation:22 Esselen Street,
Our client has an opportunity available for a Deputy Responsible Pharmacist based in Meyersdal.Requirements:BPharm qualification.1-year Regulatory Affairs or
We are looking for a Production Pharmacist on a 4 months contract to:Ensure that the Production facility operates in accordance with all the legal requirements
DSV - Global transport and logistics In 1976, ten independent hauliers joined forces and founded DSV in Denmark. Since then, DSV has evolved to become the
Main purpose of the job: To administer, maintain, and coordinate clinical trials according to good clinical practice, the study protocol, and the site standard
Main purpose of the job: To administer, maintain, and coordinate clinical trials according to good clinical practice, the study protocol, and the site standard
Time Type: Full Time Job Related Requirements: Minimum of 1 years' experience in a Pharmaceutical environment 1 year completed Community Service Ability to
Bachelor of Pharmacy Minimum 1 years experience in an Industrial or Applicant Pharmaceutical Environment (RA/QA/QC/GxP) Computer literate with prior experience
Bachelor of Pharmacy Minimum 1 years experience in an Industrial or Applicant Pharmaceutical Environment (RA/QA/QC/GxP) Computer literate with prior experience
Bachelor of PharmacyMinimum 1 years experience in an Industrial or Applicant Pharmaceutical Environment (RA/QA/QC/GxP)Computer literate with prior experience
Ensure compliant and timeous processing of regulatory submissions and commitments as assigned. Bachelor of Pharmacy Minimum 1 year Regulatory Affairs