Engineer, Quality

AbbVie Inc.

Tempe (AZ)

On-site

USD 80,000 - 110,000

Full time

4 days ago
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Benefits offered by this job

Paid time off
Medical insurance
Dental insurance
Vision insurance
401(k) plan

Job summary

AbbVie is seeking a quality-focused professional to support validation activities and strengthen the quality system across manufacturing operations in the Tempe area.

The role requires collaboration with Validation, Quality and Production teams to ensure regulatory compliance, proper investigations, CAPA documentation and robust analytics for product quality assurance.

Qualifications

  • Bachelor's degree or equivalent in Biology, Chemistry, Engineering or related field.
  • 2+ years of 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 and regulations affecting API, Bulk Drug or Finished goods manufacturing.

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.

Skills

Verbal communication
Written communication
Analytical skills
Interpersonal skills
Negotiation skills
Regulatory knowledge

Education

Bachelor's degree in Biology, Chemistry or Engineering

Job description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

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.
Qualifications
  • 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.
Compensation

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

Benefits
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.
Equal Opportunity Statement

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.

Additional Information

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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