AbbVie Posted June 17, 2026

Senior Supplier Quality Engineer

Branchburg, NJ Full-time
Quality Senior

AbbVie is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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,   Facebook ,  Instagram ,  X  and  YouTube.

Job Description

We are seeking a Senior Supplier Quality Engineer to help strengthen our supplier quality systems and ensure the highest standards of compliance, reliability, and performance across our global supply base. In this role, you will partner with suppliers and cross-functional teams to proactively identify risks, resolve quality issues, and drive continuous improvement.

Responsibilities:

Monitor the performance of suppliers on a continuous basis and escalates any potential issues to supplier quality management.

Supports the completion of supplier risk assessments and updates supplier quality database accordingly.

Ensures supplier quality database is updated timely with any new information/addition, and ensures its accuracy, i.e. Supplier evaluation criteria are maintained, and supplier files are current.

Compiles metrics for Supplier Quality Systems for internal stakeholders, tier boards and Quality System Management Review.

Communicates supplier quality-related risks to LifeCell’s business to management.

Supports internal/regulatory audits on supplier quality related requests.

Manages supplier nonconformity process, which includes but not limited to:

Ensures all supplier related NCRs are processed/closed timely.

Communicates supplier NCRs/SCARs to suppliers and necessary follow-up action are performed and documented timely per procedure requirements.

Obtains necessary documentation required from supplier to support material release at LifeCell.

Coordinates the review/approval of supplier NCRs/SCARs.

Works with suppliers to ensure supplier investigations and CAPAs are robust and will drive to root cause.

Ensures all supplier change notification records are created timely in Global TrackWise, and notifications for shared suppliers are communicated to Corporate Supplier management group timely.

Assigns assessment actions to SMEs and works with cross functional SMEs and suppliers to complete the assessments timely.

Provides feedback to suppliers in regard to change notifications and ensures necessary follow-up actions are completed as required.

Follows up to ensure required internal changes resulted from supplier change notification are implemented timely.

Coordinates the review/approval of supplier change notifications, ensures its timely closure and communicates the assessment result to suppliers as needed.

Supports the team on completing supplier audits as required per process requirements.

Qualifications

Bachelor's degree, preferably in Biology, Chemistry or Engineering

6+ 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.

Preferred:

Bachelor’s degree in Engineering is Desired

5 years’ experience with Supplier Quality, Supplier Change Notification, Supplier Audits, New Supplier Qualification, and Risk-Based supplier management is Highly Desired

Experience in Pharmaceutical or Medical Device industries is Highly Desired

Additional Note:

Willingness to travel domestically as needed, estimated to be 10% travel

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 roleat  the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors  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 isearned,  vested,  and determinable. The amount and availability of  any bonus, commission, incentive, benefits, or any other form of compensation and benefits that areallocable 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 absolutediscretion,  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

Job details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
Branchburg, NJ
Employment type
Full-time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 136 comparable Senior Quality roles across 36 biopharma companies.

136Comparable roles tracked
125Currently active
36Companies hiring similar roles
21Countries represented

Salary context

33 of 136 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $84,500/yr – $162,000/yr
Peer group range $98,050 – $219,500 (median $151,700)

Where these roles are based

Top locations among the 136 comparable roles

United States72
India15
Ireland13
Singapore10
United Kingdom4
China's Mainland3

+ 15 more countries

Seniority mix

136 of 136 peers have a known seniority level

Senior96
Associate Director26
Principal14

Therapeutic area mix

0 of 136 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
AbbVie Irvine, CA Senior
Same function Same seniority Same country
60%similar
AbbVie San Francisco, CA Senior
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Rensselaer, United States Senior
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Senior R&D Quality Officer, Product Development Quality Assurance
AbbVie · Irvine, CA · Senior
Function Therapeutic area Seniority Country
60%
Sr QA Validation Specialist (Oversight)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Specialist, Quality Assurance Lot Disposition
JuN - Seattle Dexter · Bothell, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist, Drug Product Analytical Science (ASAT), Cell Therapy
JuN - Seattle Dexter · Seattle 400 Dexter, United States · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.