Key Performance Areas: -
Support Enterprise Risk Management (ERM) Implementation
Conduct risk assessments
Risk monitoring and reporting
Insurance profile
Communication
Administer the Risk Management System
Key Requirements
Health & Safety requirements Proficient in MS Office; Excellent communication skills with the ability Conduct internal SHE trainings including SHE inductions. Organize relevant SHE trainings with service provides external stakeholders on SHE related issues SHE Officer Experience: 2-3 years preferably, (not more than
The QC Lab Analyst will be directed to perform a variety of simple to complex routine and non-routine tests to evaluate the quality of raw material (s), intermediate, finished product(s) by determining strength, stability, purity, chemical content and other characteristics. Analyse raw materials, in
ensure completion of it.
and hot work permits.
The QC Lab Analyst will be directed to perform a variety of simple to complex routine and non-routine tests to evaluate the quality of raw material (s), intermediate, finished product(s) by determining strength, stability, purity, chemical content and other characteristics. Analyse raw materials, in
Holdings is currently seeking a Temp SHEQ Compliance Officer in the Midrand area. Ensure compliance with the tools to ensure quality control and compliance. Provide management and staff training Ensure that all traceability of risk control measures and recommend changes Maintain risk registers Communicate risk control and risk Auditing Relationship building Computer literacy (MS Office) Verbal and written communication Interpersonal
Health & Safety requirements Proficient in MS Office; Excellent communication skills with the ability Conduct internal SHE trainings including SHE inductions. Organize relevant SHE trainings with service provides external stakeholders on SHE related issues SHE Officer Experience: 2-3 years preferably, (not more than
RA Associate / RA Officer to assist the RA team. You need one full year of RA Officer / RA Associate experience Regulatory Affairs Scientist / RA Associate and/or RA Officer. A working knowledge of the South African Health ethics. MUST have at least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company
Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly experienced on on SYSPRO (ESSENTIAL) Proficient on all MS Office packages Valid driver's license (no endorsements) Own Ensure that all complains responded to by the QMS officer. Assist with marketing and regulatory affairs. according to yearly schedule compiled by the QMS officer. Partakes in internal audits and compile reports Assist with training for desired level of GMP/annual GMP training. Documentation Control Ensures change