Medical Secretary Jobs in Midrand
Local Medical Safety Specialist
Manpowergroup Sa
South Africa
Seychelle, Cape Verde) Main responsibilities: Local Medical Safety Responsibility & Benefit Risk Management: the local Medical and Marketing organization in collaboration with the International Medical Safety leader Aggregate reports: Work with LSO/CSTL to provide medical input and insights for aggregate reports while regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation activities for non-medicinal products (i.e. cosmetics, medical devices, commodities, nutritional) are performed
share this job on whatsappMedical Safety Specialist Midrand
Manpowergroup SaSouth Africa
Seychelle, Cape Verde) Main responsibilities: Local Medical Safety Responsibility & Benefit Risk Management: the local Medical and Marketing organization in collaboration with the International Medical Safety leader Aggregate reports: Work with LSO/CSTL to provide medical input and insights for aggregate reports while regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation activities for non-medicinal products (i.e. cosmetics, medical devices, commodities, nutritional) are performed
Qa Ra Administrator Medical Equipment
Ultra Personnel : Pharmaceutical, Insurance, EngineeringMidrand
Reference: JHB001098-VM-1 Well known medical equipment company based in Midrand is looking for a QA / Qualifications Matric with a Degree: Science/ Medical / Biological/ Technical Experience required Advanced {Non-Negotiable} 2-5 Years working experience in the Medical Industry {Preferable} Experience with data collection analysis and trending remarks MEDICAL DEVICE FILE Managing the Group Medical Device File programs and databases
Qa Ra Administrator Medical Equipment
Midrand
Monthly
/>Qualifications
Matric with a Degree: Science/ Medical / Biological/ Technical
Experience
[Non-Negotiable]
2-5 Years working experience in the Medical Industry [Preferable]
Experience with data
remarks
MEDICAL DEVICE FILE
Managing the Group Medical Device File programs
Ra Qa Administrator
Dante Group Pty LtdSouth Africa
MID015957-TB-1 Interested in Quality Assurance in the Medical Field? Want to pursue a career in line with Audits Minimum requirements: Tertiary Qualification in a Medical-Related Field Matric is a minimum requirement 1 quality assurance or regulatory affairs in the Medical Devices or Pharmaceutical Industries, involved unsuccessful R 20000 - R 30000 - Monthly plus Medical Aid and Pension Fund
Qa Administrator Midrand
Dante Group Pty LtdSouth Africa
MID015957-TB-1 Interested in Quality Assurance in the Medical Field? Want to pursue a career in line with Audits Minimum requirements: Tertiary Qualification in a Medical-Related Field Matric is a minimum requirement 1 quality assurance or regulatory affairs in the Medical Devices or Pharmaceutical Industries, involved unsuccessful R 20000 - R 30000 - Monthly plus Medical Aid and Pension Fund
Qa Administrator Midrand
Ultra Personnel : Pharmaceutical, Insurance, EngineeringMidrand
Reference: JHB001098-VM-1 Well known medical equipment company based in Midrand is looking for a QA / Qualifications Matric with a Degree: Science/ Medical / Biological/ Technical Experience required Advanced {Non-Negotiable} 2-5 Years working experience in the Medical Industry {Preferable} Experience with data collection analysis and trending remarks MEDICAL DEVICE FILE Managing the Group Medical Device File programs and databases
Senior Regulatory Affairs Pharmacist Complimentary Medicine (cam)
Midrand
R950k - 1,000k per year medicines, including complementary medicines and medical devices for end-to-end regulatory activities.< a focus on complementary
Senior Regulatory Affairs Pharmacist: Pain, Derma & Digestive (pdd)
Midrand
R950k - 1,000k per year medicines, including complementary medicines and medical devices for end-to-end regulatory
Senior Regulatory Affairs Pharmacist: Otc
Midrand
R950k - 1,000k per year medicines, including complementary medicines and medical devices for end-to-end regulatory activities.< products, with a focus on complementary medicines and medical devices.
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