Deadline 21/11/2023, Applications are invited from suitably qualified and dynamic persons to fill the above position in a Veterinary and Public Health Chemicals manufacturing company. Job Summary: Driving the quality assurance process; the job entails the development, implementation and maintenance of integrated programs and systems that guarantee compliance to cGMP, ISO 9001, ISO 14001 and ISO 45000.
Major Responsibilities:
Responsible for compliance with regulatory requirements related to the quality of finishedproducts and driving the roadmap to cGMP compliance.
Approval of incoming materials and release of the finished product for sale.
Co-ordinating teams to formulate and implement strategies for development and maintenance of high quality standards. Supporting other departments with technical expertise towards product and processimprovement including process validations.
Ensuring all the functions of the Division are compliant with the business managementsystems; cGMP, ISO 9001, ISO 14001 and ISO 45 000, and co-ordinating internal and external audits.
As part of the Product Development team, to give technical direction on new products to be developed.
Preparation of registration dossiers, new product registrations and product stability studies. Pharmacovigilance and monitoring of field trials.
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