AbbVie Posted September 22, 2026

Quality Assurance Officer

Zwolle, OV Full-time
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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

The QA Officer has an important supportive role in the quality assurance of distribution and logistics operations and to ensure that activities continue to meet the requirements of GDP and GMP regulations.

Contributes to the development and maintenance of the Company quality policies and systems to ensure that business objectives are met for the distribution programs for AbbVie Logistics.

Providing operational support to the planning and customer service department to ensure that shipments are prepared and facilitated in a compliant manner meeting all requirements.

Contribute to the continuous improvement of the local quality system by participating and advising in new documentation change requests of procedures and SOP’s, contributing to internal audits and dealing with the investigation of distribution complaints and exceptions.

Highlighted Responsibilities:

Continuously executes the operational processes related to the assigned quality system(s)

Advises staff in relation to these systems, on how to execute the applicable activities in compliance with the GxP guidelines, AbbVie policies and other applicable regulations to ensure product quality and patient safety.

Continuously evaluates the performance of the assigned quality system through performance management (metrics) and initiates and implements improvement programs accordingly.

Maintains the documentation related to the assigned quality system, according to GDP/GMP guidelines and AbbVie policies.

Supports and executes training on good distribution and manufacturing practices and based on AbbVie’s principles of quality assurance.

Participates actively in QA projects and supports Continuous Improvement activities in the organization by participating in project working teams.

Executes the appropriate change management impacting documentation, training, and quality systems.

Contributes to the continuous improvement and compliance of the local quality system by participating and advising in new documentation change requests of procedures and SOP’s, contributing to internal audits and dealing with the investigation of exceptions.

Qualifications

Bachelor with relevant specialization, preferably in pharmaceutics, biology or another life science.

2+ years’ experience with implementing and maintaining quality systems in a pharmaceutical (GDP) environment is preferred.

Knowledge of Good Distribution Practices (GDP) and/or Good Manufacturing Practice (GMP) is considered an advantage.

Accurate, persuasive, honest, decisive, analytical, result-oriented;

Excellent writing and communication skills in English.

Preferably experience with working in SAP, or similar ERP system and TrackWise;

Able to step up and take leadership to own challenges.

Persistent and resilient when confronted with obstacles – finds the way.

Additional Information

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
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Zwolle, OV
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 1008 comparable Quality roles across 131 biopharma companies.

1008Comparable roles tracked
957Currently active
131Companies hiring similar roles
48Countries represented

Salary context

193 of 1008 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Control Stability Technician · Regeneron Pharmaceuticals, Inc (USA) $19/hr – $30/hr (≈ $39,395–$61,610/yr)
Highest disclosed · Quality Assurance Specialist · Merck KGaA $65,100/yr – $976,000/yr
Peer group range $50,502 – $520,550 (median $136,700)

Where these roles are based

Top locations among the 1008 comparable roles

United States350
Germany54
Ireland53
China53
Switzerland39
France38

+ 42 more countries

Seniority mix

498 of 1008 peers have a known seniority level

Manager160
Senior116
Intern/Fellow/Postdoc60
Associate Director40
Associate39
Director32
Principal23
Senior Director20
Executive/VP8

Therapeutic area mix

2 of 1008 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1
Respiratory1

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.

40%similar
Novartis Baarle Nassau, Netherlands
Same function Same country
40%similar
Novartis Baarle Nassau, Netherlands
Same function Same country
40%similar
Lilly Katwijk, South Holland, Netherlands Senior Director
Same function Same country
40%similar
Amgen Europe B.V. Breda, Netherlands
Same function Same country
40%similar
Johnson & Johnson Leiden, Netherlands Director
Same function Same country
40%similar
Perrigo Rotterdam, Netherlands Manager
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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.

40%
Qualified Person (QP)
Novartis · Baarle Nassau, Netherlands · Seniority not listed
Function Therapeutic area Seniority Country
40%
Specialist QA/QP (Plant QA)
Amgen Europe B.V. · Breda, Netherlands · Seniority not listed
Function Therapeutic area Seniority Country
40%
Senior Quality Affairs Officer
Mylan B.V. · Amstelveen, Netherlands · Senior
Function Therapeutic area Seniority Country
40%
Senior Specialist, QC Microbiology
BMS Netherlands Operations B.V. · Leiden – NL, Netherlands · 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.