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Abbott Quality Improvement Coordinator (Direct Labo in OpEx Dept.) in Matsudo-shi, Japan

MAIN PURPOSE OF ROLE

Individual contributor that works under limited supervision.

Applies subject matter knowledge.

Requires capacity to understand specific needs or requirements to apply skills/knowledge.

MAIN RESPONSIBILITIES

•Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements.

•Ensures compliance to the requirements from regulatory agencies.

•Maintains the technical and non-technical documentation change system.

•Assures procedures are in place to classify and maintain records.

•Interprets and enforces all documentation formatting, standards, policies, and operating procedure requirements.

•May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers.

•May analyze and evaluate data, extract pertinent information, prepare information abstracts and executive summaries of material searched.

•May maintain extensive knowledge of product information and continuous contacts with local, regional, and divisional customers.

QUALIFICATIONS

Education

Associates Degree (± 13 years)

Experience/Background

Minimum 1 year

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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