Deman Manufacturing Job Vacancy for Commercial Quality Officer | How to Apply:
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Deman Manufacturing Job Vacancy And How to Apply
Responsibilities
- Ensure that all SOPs are in place, updated & training has been conducted across the business.
- Ensure a monitoring system in place for tracking training compliance and process for escalation of persistent non-compliance. Processes in place for delivering routine training for updates to SOP.
- Promote QMS management principles and seek continuous improvement of the processes.
- Assist with planning and data collection required for QMS Management Review meetings according to local SOPs.
- Identify, Implement and Manage QA Objectives & KPIs.
- Change Control – perform day-to-day work to support the local change control process with the aim of ensuring all planned major changes (including as appropriate new pack introduction, product discontinuation, major pack changes, re-packing activities) are effective and compliantly managed. Processes in place to routinely review the progress of changes and closeout when completed.
- Risk Management – perform activities to support the risk management process to ensure effective management, timely reporting, review, and escalation of quality risks.
- Corrective and Preventative Actions (CAPA) – assist with the training and implementation of global or local processes to effectively manage corrective and preventative action plans.
Minimum Requirements
- Successful completion of relevant tertiary qualifications – Science Degree.
- At least 2-3 years of experience working in a quality and or regulatory compliance function in a Healthcare, Hygiene
- Understanding of and experience in quality assurance systems particularly in the areas of batch release, product incidents, artwork control and performing audits.
- Clear understanding and ability to assess and act upon product safety, quality, efficacy, and compliance risks.
- Clear understanding to ensure operations do not compromise the quality of products.
- Knowledge of requirements pertaining to GMP/GDP regulations.
- Knowledge on effective quality documentation systems.
- Good understanding of typical regulatory requirements relevant to a regulated product. SAHPRA Guidelines, WHO, ICH, ISO9001, ISO 13485 etc.
Job Types: Full-time, Permanent
Salary: R25,000.00 – R35,000.00 per month
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