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 Company employees, and Adverse Event and Product Quality Complaints (AE/PQC) training to distributors/3rd-Party regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation
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 Company employees, and Adverse Event and Product Quality Complaints (AE/PQC) training to distributors/3rd-Party regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation
client is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their company Job regulations. Quality Assurance Duties Quality Systems Management: Develop, implement, and maintain quality management maintenance of quality-related documentation. Ensure accurate and complete documentation of all quality processes corrective and preventive actions (CAPA) to address quality issues. Training: Develop and deliver training training programs for staff on regulatory and quality standards. Ensure that all personnel are trained and competent
looking for a Quality Systems Specialist to be based full time at our offices. The Quality Systems Specialist will be required to do the administration of the Quality management system ensuring compliance to ISO9001 SharePoint administration Exposure to management of Quality Management Systems Training and presentation to environment Key Performance Areas: Administration of all Quality Documents Drafting, checking, and collating of business practice of Control of Documents and Records Quality Monitoring and control management Engaging with
degree in Quality Management or a related qualification at an NQF 6/7 level.
* 2 Years quality management
management or Quality Assurance and /or Business Process Redesign
* 1 Year Risk Management (advantageous)
Primary Responsibilities:
Maintain the Quality management System (QMS)
* Develop and maintain
documents
* Develop, implement and validate quality standards, processes and procedures withing the
audit information
Monitor Compliance with Quality Standards:
* To audit business units'
Responsibilities
Maintain The Quality Management System (QMS)
administration
civil aviation industry. Company is looking for a Quality Assurance Generalist based in Gauteng, Midrand Midrand. Primary Responsibilities Maintain The Quality Management System (QMS) Develop and maintain QMS documents: converting documents. Develop, implement and validate quality standards, processes and procedures within the latest audit information. Monitor Compliance With Quality Standards To audit the business unit's conformance line with the international standard. Promote the quality management system and continuous improvement through
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 collection and trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO analysis and trending remarks MEDICAL DEVICE FILE Managing the Group Medical Device File programs and databases
/>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
data collection and trending
Experience with Quality Management Systems ISO 13485 or ISO 9001 or any
remarks
MEDICAL DEVICE FILE
Managing the Group Medical Device File programs
updating of Standard Operating Procedures and Quality Documents.
General administrative duties including