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1. To drive continuous Quality Improvement activities.
2. To plan, organize, supervise and co-ordinate quality compliance activities in the key result areas of documentation, and product quality related matters in all aspects of factory operations.
3. To ensure Products are manufactured to meet all Quality Standards in compliance with all applicable Regulatory requirements.
Candidate must have a strong knowledge of cGMP and current trends with regards to Quality issues in a Pharmaceutical environment.
QUALIFICATION
B. Pharm with minimum of 7years post qualification and relevant experience in Regulatory, Analytical & Production activities. M.Sc. would be an added advantage.
AGE - Not more than 37 years.
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Interested applicants should forward their application with detailed CV to the email address provided below with 2 weeks from the date of publication
E-mail address: career@evansmedicalplc.com
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