accurate mapping of clinical trial data into a harmonised database, support data acquisition processes senior staff in improving the data harmonisation platform from a clinical standpoint
Description Job Title: SHEQ Manager Location: Johannesburg, South Africa Job Description: We are looking SHEQ (Safety, Health, Environment, and Quality) Manager to oversee and ensure compliance with all health regulations at our Johannesburg facility. The SHEQ Manager will evaluate incident forms, surveys, and audits audits, working with Supervisors and Managers to address root causes and formulate corrective action plans non-compliance. Collaborate with Supervisors and Managers to address and rectify non-compliant behaviors
Quality Manager-Roodepoort-R50 000ctc Quality Qualification and minimum 5 years’ experience in a production/operations experience in laboratory testing & reporting, in a management position in a manufacturing environment. Must safety and environmental exp. Manage costs related to department, Manage quality of products and systems Control results from laboratory. The post Quality Manager Roodepoort appeared first on freerecruit.co.za
Energy industry is currently looking for an HSE Manager , in Bryanston, Johannesburg. Responsibilities: prevent recurrences. Provide guidance and support to managers and employees on health and safety matters, including all global operation emergency response plans and manage all emergency situations. Ensure safety plans and proactively. Proficiency in using health and safety management systems and related software Remuneration: R
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Regulatory Affairs Manager (POS24277)
a proactive and experienced Quality Assurance Manager to lead our quality assurance initiatives. As a identify areas for improvement. Analyze quality data to identify trends, root causes of issues, and implement and ensure adherence to established QA processes. Manage documentation related to quality assurance activities and audits. Quality Responsibilities Quality Management Systems (QMS): Develop, implement, and maintain effectiveness of QMS. Conduct internal audits and manage external audits. Process Improvement: Identify
Regulatory Affairs Manager (POS24191)
Area: Aeroton
R1 external partners and Principals, and to control and manage portfolio and team outputs. To ensure legal compliance and maintenance lifecycle
Key Job Outputs
corrective action. Analyse quality data and generate reports for management. Ensure that manufacturing processes Controls to ensure that spend is appropriately managed and cost saving inititaives identified and initiated complaints. Bachelor's degree in Engineering, Quality Management, or a related field. At least 5 years experience
implementing a GFSI system.
job: The project manager/study coordinator is responsible for coordinating all clinical trial activities activities according to good clinical practice, the study protocol, and the site's standard operating procedures performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist efficient study start-up, conduct, and close-out Manage regulatory updates throughout the study (New ICFs resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Communicate with