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.

For more and on how to apply click download below


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