issues.
SAFETY issues.
Incumbent
manage a team of analysts and drive the technical department ensuring that ISO 17025 validations are planned submit, as well as all other functions within the department are followed through and done correctly. Minimum a team of analysts and driving the technical department ensuring that ISO 17025 validations are planned
manage a team of analysts and drive the technical department ensuring that ISO 17025 validations are planned submit, as well as all other functions within the department are followed through and done correctly. Minimum a team of analysts and driving the technical department ensuring that ISO 17025 validations are planned
Associate experience within the regulatory affairs department at a pharmaceutical company to apply. The role tasks. Faxing, filing, liaising with various departments and regulatory bodies, following up with SAHPRA
Associate experience within the regulatory affairs department at a pharmaceutical company to apply. The role tasks. Faxing, filing, liaising with various departments and regulatory bodies, following up with SAHPRA
licenses and provides actuarial services to departments within the company. The position will report
licenses and provides actuarial services to departments within the company. The position will report
document control functions within Randburg SHEQ Department. KEY OUTPUTS Quality Assurance: 1. Compile Quality questionnaires with support from the relevant Departments. KEY COMPETENCIES - Strong interpersonal and
compliance.