HR Leverage Africa Senior Quality Assurance Supervisor Jobs in Nigeria
HR Leverage Africa Senior Quality Assurance Supervisor Jobs in Nigeria
Job Responsibilities Prepare/revise operating procedures and specifications
Review/approve routine change control requests as designated
Review and approve suppliers / service providers including supporting with audits of critical suppliers where required
Control of product labeling/label accountability
Support the Quality Manager in the determination of training requirements for the Quality Assurance team. Act as trainer and lead training for the Quality Assurance Officers in specific SOPs as required
Lead root cause analysis and corrective and preventive actions for audit observations, product complaints, product non-conformances, in-process deviations issues related to process controls
Monitors and ensures that batch records are audited per manufacturing/packaging/shipping requirements, when required.
Lead and perform data review audits (Batch Production Records, Validation Documents and Development Documentation, Quality Control Data as required)
Support the Qualified Person and Quality Manager in the definition and maintenance of the annual internal and external audit programs.
Verify that all documentation is complete
Document non-compliance and evaluate if further investigation is needed
Enter test results or summaries into the pharmacy specific monthly and quarterly Quality Assurance report template
Document results of deviation and complaint investigations, causal analysis, corrective actions and preventive actions
Support the Quality Manager with hosting customer audits and regulatory inspections
Maintain quality records (equipment calibration and maintenance, training, deviation and complaint investigation, environmental monitoring, Certificate of Analysis, clean room certification etc.).
Job Requirements
5 plus years relevant experience in the regulated pharmaceutical industry, specifically including Quality Assurance, Quality Control, and/or Drug Regulatory Affairs
B.Sc in Applied Sciences, especially Chemistry, Biochemistry, Industrial Chemistry.
Post-graduate degree is a plus.
Good understanding of the pharmaceutical market, including the
unlicensed medicines sector.
Understanding of pharmaceutical manufacturing and laboratory work (including familiarity with various analytical techniques) a strong asset
Competent in computer packages including Microsoft Office and an electronic quality management package
Knowledge of tools, concepts and methodologies of QA
Solid experience in effective usage of data analysis tools and statistical analysis
Knowledge of relevant regulatory requirements
Emotional resilience and an ability to work under pressure with a "can do attitude".
Ability to process a high volume of planned and un-planned work effectively
The ability to multitask and manage time effectively to ensure all work streams are managed.
How to Apply
Interested and qualified candidates should forward their CV to:
consulting.hrla@gmail.com using the "Job title" as the subject of the application.
Note: Only qualified candidates should apply.
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