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Engineer, Quality

AbbVie

Tempe, AZJob$66K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
$66K/yr
Location
Tempe, AZ
Work Authorization
Not specified

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Job overview

The Quality Engineer carries out Manufacturing Quality Assurance functions at the plant, including deviation resolution, product impact analysis, corrective and preventive actions, investigations, SOP approval, calibration oversight, and quality improvement. The role supports compliance with cGMP, company policies, and applicable regulations, and works with plant departments and other Quality areas to meet quality goals.

Skills & qualifications

RequiredNice to have

Skills

ValidationQuality SystemsRegulatory ComplianceInvestigationProduct Impact AnalysisStatistical Quality ProgramsAcceptance SamplingCommunicationProblem SolvingAnalytical SkillsInterpersonal RelationsNegotiationQuality Compliance ManagementAPI ManufacturingBulk Drug ManufacturingFinished Goods Manufacturing

Qualifications

Bachelor's in Biology, Chemistry, Engineering or Equivalent Experience2+ Years Manufacturing, Quality or Engineering Experience

Benefits

Paid Time Off
Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Company 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, (https://www.linkedin.com/company/abbvie/) Facebook, Instagram (https://www.instagram.com/abbvie/) , X (https://twitter.com/abbvie) and YouTube. (https://www.youtube.com/user/AbbVie)

Job Description

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.

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.

Additional Information

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.

  • 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.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

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 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

Salary: $65,500

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