Job Description

Role & responsibilities Documentation is the key to GMP compliance and ensures traceability of all development, manufacturing, and testing activities. Documentation provides the route for auditors to assess the overall quality of operations within a company and the final product. Quality Management System (QMS) is ensuring that drugs are safe, effective, and of high quality is fundamental, as these factors directly impact patient health. Quality management systems are essential across the industry to uphold these stringent standards. • Officer - Documentation & QMS ensures that all documentation is clear and concise, and that it's followed by all personnel. This helps to ensure that the manufacturing process is consistent and safe. • Officer - Documentation & QMS play a critical role in ensuring that the pharmaceutical industry complies with a wide range of regulatory requirements and international standards. This involves preparing and submitting regulatory documents and conducting audits and inspections to ensure compliance with regulations. • He/she should have familiarity with guidelines such as GLP, FDA and cGMP regulation and principles of Quality Management. • Officer - Documentation & QMS will provide technical and general administrative support to this department and ensure that tasks are carried out in a timely manner, Preferred candidate profile Perks and benefits