Description:
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
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24 Jan 2026;
from:
gumtree.co.za