Quality Specialist

Компания "Abbott Laboratories"

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:

• Career development with an international company where you can grow the career you dream of.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

At Abbott, we believe people with diabetes should have the freedom to enjoy vigorous, active lives. Our systems help people with diabetes manage their health more effectively and comfortably with easy-to-use products that provide accurate data to drive better informed decisions.

We are now looking for Quality Specialist (Abbott Diabetes Care).

What You’ll Do

• Ensure Quality System awareness and compliance in the Region
• Plan and conduct internal audits / assessment to verify the effectiveness of the management system
• Receive audit input and follow QS Document Control
• CAPA management follow up and ensure closure
• Ensure QS record keeping, Warehousing, Quality Holds, Supplier / Distributors evaluation/monitoring/audit
• Coordinate Field Communications at the Region
• Ensure availability of org charts (including LSME) and job descriptions
• Be the expert on QS process and support the rest of team, train timely
• Work in close cooperation with regional QA manager, to build and continuously improve efficient, transparent and smooth documents process

Key Requirements

• Higher education
• Scientific background (i.e. Lab Technician, Biology, Chemistry, Pharma, M.D.)
• At least 3 years of experience in quality of medical devices a must
• Product and market environment knowledge preferred
• Quality Systems management and auditing experience
• Management skills and leadership competencies
• Excellent English (writing, speaking, negotiations)
• Experience of work in international environment/projects
• Cultural sensibility

The stated job description, as well as the list of job requirements, is not complete.

This position opens for staff replacement.

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