Amgen Europe B.V. Posted August 6, 2026

Manager Incoming Quality

Breda, Netherlands Full time
Quality Manager

Amgen Europe B.V. 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

Career Category

Quality

Job Description

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission, to serve patients, drives all that we do. It is key to becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together, researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us as:

QA Manager – Incoming Quality Assurance (IQA)

At Amgen Breda medicines are labelled, assembled, stored and eventually shipped to various countries worldwide. Every day more than 1000 people with 42 different nationalities are working on supply chain processes, manufacturing, marketing and sales of our medicines and clinical research into new medicines.

Live

What you will do

In this vital role, you will lead the Incoming Quality Assurance (IQA) team in Breda, ensuring high standards of quality and compliance across incoming materials and processes. You will play a key role in shaping a strong quality culture while developing and empowering your team to perform at their best.

You will oversee the end-to-end Incoming Quality processes, ensuring they are executed efficiently, consistently, and in full compliance with GMP and regulatory requirements. At the same time, you will act as a key decision-maker within QA, bringing a risk-based mindset to quality-related topics.

Your main responsibilities will include:

Leading, coaching, and developing the IQA team, including hiring and performance management

Ensuring effective sampling, inspection, and disposition of incoming materials

Reviewing and approving deviations, CAPAs, and change controls in line with quality standards

Acting as Subject Matter Expert (SME) for Incoming Quality and driving continuous improvement initiatives

U se of digital tools and technologies to analyse team performance and identifying most valuable improvements’

In addition, you will work closely with cross-functional stakeholders and contribute to broader quality and business objectives by:

Supporting audits (internal and external) and ensuring inspection readiness

Driving process improvements and participating in key projects and programs

Collaborating with Supply Chain, Manufacturing, and Warehouse teams to ensure alignment and operational excellence

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The QA Manager we seek is a strong leader with the following qualifications:

Minimum Qualifications:

Master’s degree in Pharmaceutical Sciences, Life Sciences, or equivalent

+3 years of experience in a GMP-regulated environment

Experience in people management

Proven experience in investigations, CAPAs, and process improvement

Preferred Qualifications:

Experience in the pharmaceutical industry

Experience in supplier management

Familiarity with deviations, CAPAs, and change control processes

Knowledge of risk management tools (e.g., FMEA)

Key Competencies:

Strong leadership and team development skills

Effective communication across multiple stakeholders

Analytical mindset with a risk-based approach

Decision-making skills and ability to manage complexity

Continuous improvement of mindset and interest in new technologies

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we work to care for our teammates’ professional and personal growth and well-being. Therefore, Amgen is regularly recognized as a Best Place To Work ©.

Vast opportunities to learn and move up and across our global organization.

Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.

Generous Total Rewards Plan comprising competitive salary, bonus structure, fixed 13th month, holiday allowance and a collective health insurance.

Focus on vitality with an on-site gym, vitality program and a restaurant with healthy food.

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Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Breda, Netherlands
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 164 comparable Manager Quality roles across 50 biopharma companies.

164Comparable roles tracked
151Currently active
50Companies hiring similar roles
25Countries represented

Salary context

44 of 164 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 Not listed on this posting
Lowest disclosed · Associate Specialist, Quality Control, Lab Support · Merck $65,100/yr – $102,500/yr
Peer group range $83,800 – $219,500 (median $163,000)

Where these roles are based

Top locations among the 164 comparable roles

United States73
China16
Ireland15
India14
Japan9
Singapore6

+ 19 more countries

Seniority mix

164 of 164 peers have a known seniority level

Manager115
Associate Director26
Associate23

Therapeutic area mix

0 of 164 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.

50%similar
BMS Netherlands Operations B.V. Leiden – NL, Netherlands Associate
Same function Adjacent seniority Same country
45%similar
AbbVie North Chicago, IL Manager
Same function Same seniority
45%similar
Novartis Carlsbad, United States Manager
Same function Same seniority
45%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority
45%similar
Gilead Sciences, Inc. La Verne, United States Manager
Same function Same seniority
45%similar
Gilead Sciences K.K. Tokyo, Japan Manager
Same function Same seniority

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.

50%
Associate, QC Systems and Support
BMS Netherlands Operations B.V. · Leiden – NL, Netherlands · Associate
Function Therapeutic area Adjacent seniority Country
45%
Manager, Quality Assurance Compliance
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Quality Assurance (GMP Operations)
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
45%
Microbiology Manager
Mylan Teoranta · Inverin, Ireland · Manager
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.