- Ensure awareness and compliance of new and revised quality documents and regulations that affect the assigned area of responsibility.
- Supports the business in the region according to the position expertise and functions.
Ensure Quality System awareness and compliance in the Region :
- Plan and conduct internal audits / assessment to verify the effectiveness of the management system
- Perform supplier/ distributors audits as required. Prepare/ coordinate external audits.
- CAPA management follow up and ensure closure.
- Ensure QS record keeping, Warehousing, Quality Holds, Supplier / Distributors evaluation/ monitoring.
- Coordinate Field Communications at the Region.
- Ensure availability of org charts (including LSME) and job descriptions.
- Support/provide training to the organization about the ADD Quality System.
- Set and track the Training Plan for all positions. Maintain continuous vigilance upon the employee compliance with trainings, to contribute prevent late trainings.
- Process Team Subject Matter Expert: Be the expert on a QS process and support the rest of team as process SME.
Background
- Fluency in English is a must. (Arabic language is an advantage).
- At least 2 years of experience in the diagnostic industry (preferred), medical device or related health industry (commercial affiliate or manufacturing) or clinical laboratory.
- Product and market environment knowledge preferred.
- Quality systems management and auditing experience desirable.
- Management skills and leadership competencies.
- Experience to work in international environmental projects.
- Operates under Quality and Regulatory Directives and Abbott policies and procedures.
- Follows local regulations.
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