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Abbott Quality Assurance Specialist in Matsudo-shi, Japan

MAIN PURPOSE OF ROLE

• Individual contributor representing the most common entry point for this career stream.

• Works under direct supervision.

MAIN RESPONSIBILITIES

• Primary responsibility is ensuring implementation of quality plan at every stage of the Clinical Trial process/operations.

• Implement quality assurance regulations.

• Write and revise standard operating procedures.

• Support and facilitate audits and regulatory inspections.

• Support Quality Assurance Manager in supervision of all quality control aspects of the process (laboratories studies, clinical research, testing, operations).

• Ensure that standards are met and report potential issues either with quality or reliability of testing procedures.

• Lead implementation of new regulations.

• May support quality training.

QUALIFICATIONS

High School Diploma / GED

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email corpjat@abbott.com

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