Deadline 21/11/23, Applications are invited from suitably qualified and dynamic persons to fill the above position in a Veterinary and Public Health Chemicals manufacturing company.
Quality control, Validation, Stability studies, analytical method development as well as implementation and maintenance of systems that guarantee compliance to cGMP, cGLP, ISO 9001, ISO 14001 and ISO 45001 Major Responsibilities:
Responsible for analysis of raw materials, in-process materials, finished products as well as
research and development samples as head of QC.
Perform validation and stability studies in compliance with systems, standards and regulatory requirements.
Collaborate with other departments in performing research and development activities.
Supporting other departments with technical expertise towards product and process
To ensure that all the Laboratory functions are compliant with the business management systems; cGMP, cGLP, ISO 9001, ISO 14001 and ISO 45001.
Participate in internal and external audits to which the company management system subscribes to
For more and on how to apply click download below