Live opening · Posted 8 hours ago

Digital Quality Engineer

AbbVie · Tempe, AZ, United States
Smartrecruiters No Full-time
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At a glance

The key details from the original listing.

Posted 8 hours ago
CompanyAbbVie
LocationTempe, AZ, United States
Job typeFull-time
Work modeNo
SourceSmartrecruiters
ListedPosted 8 hours ago

About the role

Description supplied by the original job listing.

The Quality Engineer is responsible for carrying out Manufacturing Quality Assurance functions within the plant including resolution of deviations, performance of product impact analysis and corrective and preventive action for events, leading and participating in investigations, approval of standard operating procedures, oversight of the plant calibration program, quality improvement programs, and assurance of cGMP and Abbott policy compliance for the manufacturing plant.
Responsibilities
Assist Validation Engineer in the validation and certification of all new process equipment and periodically review all certified systems to assure the capability of meeting quality requirements.
Responsible for implementing and maintaining the effectiveness of the Quality System.
Support to ensure that all quality goals are met, and all practices and procedures comply with company policies and applicable regulations.
Ensures investigations of plant events are completed thoroughly and documented accurately and are included in the plant CAPA system. Performs product impact analyses for plant events and places product on QA hold where appropriate.
Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments.
Participates on the Validation Review Board as the Manufacturing Quality Assurance function.
Approves standard operating procedures; ensures procedures comply with policy and make
sense.
Approves calibration requests and ensures that these requests have appropriate product/process limits assigned.
Develop and implement statistical quality programs, assure all acceptance sampling is capable of meeting expected product quality confidence levels for manufactured as well as purchased materials.
Bachelor's degree, preferably in Biology, Chemistry or Engineering or equivalent related experience
2+ years of overall experience in Manufacturing, Quality or Engineering
Good verbal and written communication skills.
Good problem solving and analytical skills
Good interpersonal relations / communications skills
Good negotiation skills
Knowledge of quality / compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing.

Employment type
Full-time

Work arrangement
No

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