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Engineer, Quality

AbbVie · Tempe, AZ

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Level
Engineer
Team
Quality
Degree
Required (or equivalent experience)
Experience asked
2+ years
Industry
Pharma & life sciences
Posted
10 days ago

The role in 30 seconds

An engineer-level quality role at AbbVie (pharma & life sciences) in Tempe, AZ. 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.

They ask for
2+ years · degree required (or equivalent experience)
Tools it names
CAPA, Validation (IQ/OQ/PQ)

Read from the posting. The full description is below.

How this role compares

Against 29 other live quality postings in Arizona.

Base pay
Not listed in this posting

Typical $112k–$165k, from 10 postings that list pay.

Experience asked
Less than usual (2+ vs 5+)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • Root cause 60%
  • ✓ Validation (IQ/OQ/PQ) 60%
  • Supplier quality 50%
  • New product launch 50%
  • FMEA 40%
  • SPC 30%

✓ = this posting asks for it too. % = share of similar postings that mention it.

It asks for 2+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone on the team first.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at AbbVie

    We found 3 people at this company and state: 3 on the team. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

    Write to Kristin → (free)
  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: AbbVie in Tempe

1 other open role at this site · 3 people we found on the quality team.

Full description from AbbVieAs posted on their careers site.Show

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.
Show full 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.

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