Quality Assurance Engineer- Temporary 12 months

PURPOSE STATEMENT 
Ensure that our product is functional and safe for the end customer by understanding developing and applying quality control systems as well as analyzing proposing and implementing improvement of quality and manufacturing processes thinking about improving defects in a timely and efficient manner.

MAJOR RESPONSIBILITIES 
Evaluate propose and implement low complexity improvements in processes in the process quality area seeking to strengthen processes while improving their efficiency guided and advised by the area manager.
Search for solutions to problems identified in the areas of manufacturing and process quality through the application of Lean tools.
Support assigned root cause investigations (NCRs) as well as the development of action plans and the implementation of corresponding actions during the established period of time. Review and Approve documents for Low Impact NCR.
Review and approve quality plans and First Article Plans related to the production process with low to Low complexity as well as propose changes to PFMEAs this for those projects where you are assigned as a Quality representative.
Perform reviews to OT Core System documents as well as validation/qualification protocols (IQ PPQ IOQ IO PR etc.) where assigned as a quality representative for simple equipment/system.
Provide support to key company projects including definition and implementation of controls aimed at ensuring product quality.
Ensure the order and cleanliness of the areas under your responsibility. (5s) and comply with quality GOs in the corresponding period.
Do the other functions inherent to the position and those assigned by your immediate manager.
Meet compliance with corporate and legal EHS requirements by complying with internal policy and addition ensure compliance through the adoption of necessary strategies internal controls communication and training.
Continuously maintain EHS results through leadership commitment and participation in all EHS-related initiatives.

Qualifications :

EDUCATION 
Bachelors degree in Industrial Engineering Bussiness Administrator or related career.
Desirable CQE (CERTIFIED QUALITY ENGINEER certification) given by ASQ.
Basic/intermediate English proficiency.

Experience of at least 2 years in the quality department in the medical industry.

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time