Key performance areas will include, but are not limited to:
Identifying, validating, and implementing QC analytical methods and equipment/systems
Investigating QC incidents and out-of-specification results
Monitoring and reporting performance of inhouse controls and reference standards
Implementing and maintaining a competency-based cGMP training system that meets business and regulatory requirements
Executing of training related administrative requirements independently and in conjunction with relevant stakeholders where required
Quality Assurance general support
Key Requirements: A relevant qualification in Quality or cGMP and/or a relevant training qualification with at least 5 years experience in a pharmaceutical manufacturing or quality assurance environment, with working knowledge of cGMP, pharmaceutical facilities, processes, equipment, and systems. Additionally the candidate should have at least 2 years' experience in a training role and possess knowledge of adult learning theory, instructional design, and effective training methodologies. Additional Requirements: Computer literacy, excellent verbal and written communication skills, strong independent/cross-disciplinary skills, attention to detail, and good interpersonal communication and presentation skills with personnel from multiple departments and employee levels. *Only candidates that meet all the requirements should apply **Only candidates that are shortlisted will be contacted By sending your application to Scistaff you consent that your information may be kept in accordance with the requirements of the POPI Act.