Job Summary
Responsible for enforcing all validation activities. This includes the validation master plan (MP) and all activities related to equipment, utilities, facility, cleaning and vendor validation. Also responsible for all validation SOPs. Additionally, responsible for providing leadership and training to the validation team to foster a culture of compliance to all set standards of quality especially WHO GMP standards
Responsiblities
Prepare, review, and update validation SOPs and the validation masterplan
Design procedures, protocols, and report templates.
Oversee all validation activities, including equipment qualification, process validation, and cleaning validation
Ensure computer systems validation and validation sample analysis are completed on schedule.
Conduct risk assessments and address mitigation measures
Compile and submit validation reports/protocols to the QA Manager.
Promote cGMP compliance through training and selfinspections.
Identify opportunities to improve quality management systems
Assess and ensure equipment, processes, and utilities meet specifications.
Provide validation updates and propose Continuous Improvement Plans (CIP).
Competencies, Qualifications & Experience
Attention to detail and an affinity for high standards.
Excellent verbal, written, organizational skills.
Good people management skis
Computer Literacy Le Ms. Word, Excel, PowerPoint, Access etc.
Minimum Degree in Chemistry. Pharmacy or its equivalent
Minimum three (3) years’ experience in pharmaceuticals manufacturing industry: at least two (2) of which should be in quality operations (Inprocess) in a supervisory capacity.
Excellent understanding of cGMP and concepts of quality management system
Deadline: 31 March 2025, COB Send application to recruitment@cosmospharm.com .Only shortlisted candidates will be contacted
Apply via :
recruitment@cosmospharm.com
