currently seeking a Temp SHEQ Compliance Officer in the Midrand area. Ensure compliance with the Food Safety and SHERQ procedures and checklists. Operational Compliance Support and Auditing Co-ordinate the development maintain quality tools to ensure quality control and compliance. Provide management and staff training Ensure on-site inspections and respond to regulatory non-compliance Maintain the HACCP system and other safety information emergency services with regard to local governmental compliance requirements and best practice. Conduct post
environmental-related topics (noise levels, use of machinery, spillages, Health, security compliance, etc.).
principles.
them in accordance with Company guidelines and legal requirements.
for a Health and Safety Officer to ensure legal compliance to OHS Act and applicable regulations bu assisting health and safety policies and procedures in compliance with local and federal regulations Provide training
for a Health and Safety Officer to ensure legal compliance to OHS Act and applicable regulations bu assisting health and safety policies and procedures in compliance with local and federal regulations Provide training
currently seeking a Temp SHEQ Compliance Officer in the Midrand area. Ensure compliance with the Food Safety and SHERQ procedures and checklists. Operational Compliance Support and Auditing Co-ordinate the development maintain quality tools to ensure quality control and compliance. Provide management and staff training Ensure on-site inspections and respond to regulatory non-compliance Maintain the HACCP system and other safety information emergency services with regard to local governmental compliance requirements and best practice. Conduct post
the clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate well with requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings systematic in approach to tasks, with strict compliance to protocols Exceptional organizational and administrative
the clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate well with requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings systematic in approach to tasks, with strict compliance to protocols Exceptional organizational and administrative
the quality control of patient files and data entries (i.e., eCRF’s, CRF’s)