Hartalega is made up of a tight-knit, passionate and highly-skilled set of individuals. From our top executives, to our line technicians; we are all proud to be part of an elite group responsible for revolutionising the glove-making industry.
Own or contribute to root-cause analysis, corrective actions and preventive improvements so recurring incidents are reduced rather than repeatedly worked around.
Strong understanding of GMP requirements, pharmaceutical engineering standards, and regulatory expectations, with experience in preparing and maintaining technical documentation.
Independent and self-responsible implementation and quality assurance of product increments, including test automation, CI/CD integration, security and compliance testing, and defect management.
You will lead technical discussions and architecture reviews within the engineering team, providing thoughtful feedback and driving decisions that improve system design
Review contract documents, project specifications, evaluate project risks and ensure technical compliance to Customer’s requirements and Industry Codes and Standards.
Review contract documents, project specifications, evaluate project risks and ensure technical compliance to Customer’s requirements and Industry Codes and Standards.