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Job Description
- Act as an internal Auditing for following and updating current ISO certificates
- Assist in setting and maintaining a quality plan to bring the Company’s Quality Systems and Policies into compliance with quality system requirements
- Review relevant GMP documents for compliance to company SOPs, quality systems, and regulatory requirements.
- Ensure all investigations are performed and closed in a timely fashion. Monitor and report adverse events
- Reviewing Validation Master Plan & Validation Documents.
- Oversee the following investigations: nonconforming product, customer complaint, laboratory out-of-specification, and corrective and preventive action.
- Prepare and conduct the Quality Management Review meetings with senior management also ensure that Quality Objectives are set by top management for measuring the performance of the QMS.
- Support/Provide training to the organization in order to build quality awareness & cGMP concepts
- Reviewing batch records, all its related documents in order to be released for the market
- Perform Supplier/Distributors audits as required.
- Prepare/Coordinate external audits.
- Responsible for Risk Management system.
Job Requirements
- Science, Pharmacist, Veterinarian.
- 10 -15 years’ experience in Quality Assurance or the pharmaceuticals manufacturing
- Knowledge about the standard quality system
- Computer skills.
- Self-modified, good leader, trainer skills
- English Language
