Associate Professional Quality

vor 2 Wochen

Wiesbaden, Deutschland Abbott Laboratories Vollzeit

**About Abbott**

Abbott is a global healthcare leader, creating breakthrough science to improve people âs health. We âre always looking towards the future, anticipating changes in medical science and technology.

In Germany, Abbott has more than 3,000 employees working in manufacturing, research and development, logistics, manufacturing, sales and marketing. They are located at Abbott's German headquarters in Wiesbaden and its sites in Hanover, Neustadt am Rabenberge, Wetzlar, Eschborn, Cologne, Jena and Hamburg.

**Working at Abbott**

At Abbott, you can do work that matters and help people to live a healthier and full life, grow your career, and learn, be your true self. You will have access to:

- Career development with an international company where you can grow the career you dream of
- An attractive benefits package (e.g. attractive Abbott Pension Plan, a company bike, employee stock purchase program)
- 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
- A challenging position in a fast-growing crisis independent industry
- To become part of a dynamic, highly educated, highly skilled, and motivated team
- Flat hierarchies, open appreciative mentality, and efficient, constructive lines of communication
- Multi-national environment, where we foster the development of our talents within the enterprise

**The Opportunity**

This position works out of our Wiesbaden location (Abbott Diagnostics GmbH) in the European Distribution Center (EDC).

The position will be preliminary limited to 2 years.

**What You Will Do as Associate Professional Quality**

Conducts quality-related activities to deliver consistent, high quality documents, services, products and processes.

**Major Responsibilities**
- Maintains awareness of industry regulatory standards.
- Ensures compliance to site level policies and procedures by promptly reporting non-compliance issues to the department manager.
- Ensures Audit Commitments are executed on time.
- Supports upcoming inspections/audits including inspection logistics.
- Communicates effectively on risks that could impact Compliance.
- Timely executes project activities e.g. IVDR implementation.
- Performs inspection and approval of production documentation and final product release (MQA).
- Carries out inspection and approval of incoming materials and/or printed materials (IQC).
- Performs inspection and verification of in process testing documentation.
- Acts as author/initiator or quality approver for validations of Test Methods and Processes as well as qualifications of facilities, utilities and equipment.
- Initiates, reviews and approves Periodic Validation Reviews.
- Participates as Member in Cross Functional Teams regarding validation topics..
- Executes reliably Quality Tests (e.g. Analytical Tests, Customer Release Tests and Stability Tests) within established timelines.
- Conducts quality-related activities related to the CAPA process to deliver consistent, high quality documents, services, products and processes.
- Supports implementation of CAPA-specific process improvements.
- Executes projects within the Quality area.
- Performs Incoming Quality Inspections of TPM and /or printed materials.

**Education**
- Apprenticeship or Bachelor degree in Life Science, Engineering, or closely related discipline is required OR relevant combination of education or experience.

**Background**
- 0-2 years’ work experience in this job area.
- Entry level position.
- Quality or related field experience preferred.
- Demonstrates basic understanding of regulatory requirements in the healthcare environment.
- Good written and spoken English skills.

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