On behalf of our client, a global pharmaceutical company, we are currently recruiting for a Quality Analyst.
Management and maintenance of the Quality documentation system. Issuance and tracking of change controls, deviations, CAPAs, complaints, etc. Life-cycle management of SOPs, Forms and other related documents for all departments. Have the capacity to train personnel on salient aspects of the Quality System, e.g., for SOP updates, and mentor and instruct others on the correct use of it. Be the main point of contact for personnel for documentation/systems related matters. Be involved in the development and implementation of different aspects of the Quality System that will be rolled out across the group. Assist in the development and execution of annual GMP training. Assist in the development and presentation of Quality metrics to Corporate. Adherence to Company Health & Safety procedures Participate in training programmes
Bachelor's degree in science is required. Detail oriented, approachable, and collaborative. Proven communication skills. Exposure to International Pharmaceutical Practices and Requirements. Minimum 3 years Pharmaceutical experience preferable with a global pharmaceutical organisation, experience should be in quality assurance, quality control or manufacturing A thorough understanding of Quality Systems and cGMP' Experience with and a fundamental understanding of European GMP's Results and performance driven - deliver results that meet or exceed expectations Sense of urgency - responding to issues and opportunities in a timely manner Take ownership and accountability for activities Positive and pro-active approach to business tasks
To apply for this role please send CV to or call Linda on .