Tshwane Metro, Pretoria, Brooklyn
The Specialist Network Manager is responsible for identifying, evaluating, and regulatory compliance. The Specialist Network Manager serves as a primary point of contact for providers
responsibilities as given by the Laboratory/Technical Manager Recording data accurately and promptly and in compliance objectives Responsible for ensuring that the management system related to quality is followed at all the quality management system and laboratory processes are effected Participate and assist with assessments assessments by external bodies to evaluate the Quality Management System Participate in routine Proficiency testing
position will report to the QC (Quality Control) Manager. NOTE - For now, the positions are on an 18-month testing. And perhaps to stand in as Acting QC Manager from September too. Job functions: Lead validation
Assurance Manager to join their company. Requirements: Post-matric studies in quality management systems improvement initiatives. Responsibilities: Manage and report quality management systems. Audit the QMS, processes processes, and products. Management review. Health and safety monitoring and improvements. Monitor International the company concerning 3rd party audits. Chair management review meetings. Maintain environmental health service quality meets industry standards. Lead and manage a team of quality assurance specialists, providing
s
- Manage Regulatory Requirements
- Approve or Decline manager approval cases
manager approval cases and recommendations
- Assist manager with the identification
failure of the policies
- Ensure that all manager approval ,correspondence and resubmissions are
are all finalized at month end
- Compile manager approval report weekly/monthly
- Compile and
and management with a coaching feedback report.
- Review clients on QC tools
- Assist with
quality testing as well as the bacterial laboratory o Assist in reception of documentation o Responsible for the state department, ISTA and ISO/IEC 17025. o Assist with archiving in compliance with the protocols the state department, ISTA and ISO/IEC 17025. o Assist in the stock control of chemicals, kits, reagents Sheets on file current. o Assist in the maintenance of Books of Life. o Assist with the ad hoc reparation bacterial laboratory o Assist in planning and scheduling of sample processing. o Assist in arranging and allocating
responsibilities as given by the Laboratory/Technical Manager Recording data accurately and promptly and in compliance objectives Responsible for ensuring that the management system related to quality is followed at all the quality management system and laboratory processes are effected Participate and assist with assessments assessments by external bodies to evaluate the Quality Management System Participate in routine Proficiency testing
responsibilities as given by the Laboratory/Technical Manager
settings. Customer relations and relationship management. Working in a clinical environment and interacting The development of research protocols and the management and organization of data (user studies) User RETSPL studies, and clinical validation studies. Managing all aspects of the research study. Develop research writing up of claims studies. Documentation: 25%. Assisting the Legal & Regulatory team with required
settings. Customer relations and relationship management. Working in a clinical environment and interacting The development of research protocols and the management and organization of data (user studies) User RETSPL studies, and clinical validation studies. Managing all aspects of the research study. Develop research writing up of claims studies. Documentation: 25%. Assisting the Legal & Regulatory team with required