Johnson & Johnson Posted September 22, 2026

EMEA Staff Quality Specialist Service & Repair, Orthopedics

Amersfoort, Netherlands Full time
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Johnson & Johnson 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

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Customer/Commercial Quality

Job Category:

People Leader

All Job Posting Locations:

Amersfoort, Utrecht, Netherlands

Job Description:

We are looking for EMEA Staff Quality Specialist Service & Repair, Orthopedics to make a meaningful impact on the quality and reliability of medical device service and repair. As the Staff Quality Engineer – Service Quality, you will serve as a trusted quality and compliance partner for assigned DPS Service Centers, helping teams consistently execute Quality System requirements and deliver dependable outcomes for customers and patients.

In this highly collaborative role, you will work across Service Operations, Customer Quality, and other key functions to strengthen and harmonize service processes, deploy quality agreements and training, and promote consistent practices across assigned sites. You will use data, risk-based thinking, and structured problem-solving to monitor performance, address nonconformances, CAPAs, and audit observations, and identify opportunities for continuous improvement. This is an opportunity to influence quality beyond a single site, lead cross-functional initiatives, and help shape a compliant, efficient, and continuously improving global Service & Repair network.

DUTIES & RESPONSIBILITIES

Be the main point of contact for quality and compliance aspects for assigned WW Service Center(s) in the assigned Region

Ensure general compliance support for consistent and correct execution of QS procedures at all Service Centers e.g. change management strategies

Coordinate the Regional Quality Plan and provide regional oversight of QMS execution and identify systemic compliance gaps across sites.

Be the subject matter expert for the validation of equipment and computer system validation of equipment

Ensure qualification and management of Suppliers related to Installation & Servicing

Collaborate with Service Operations and Field Service to ensure global harmonization of service processes.

Collaborate with Customer Quality representatives to ensure compliance with reporting requirements of all Service centers and accuracy of service evaluations linked to customer complaints

Support tracking of monthly performance and quality metrics for each Service Center and attend the monthly/annual review meetings

Coordinate and support resolution for all nonconformances, CAPAs and audit observations related to Installation and Servicing for the Netherlands Service Center and regional QMS

Collaborate on shared/global procedures update and harmonization

Support Service Sites internal and external audits based on sites requirements

Conduct training related to procedural changes and coordinate with relevant stakeholders to investigate and document deviations identified at the sites.

Manage the initiation and review of Service Level Agreements

Responsible for communicating business related issues or opportunities to the next management level

Conduct data driven analysis based on requirements

Lead continuous improvement initiatives to ensure efficiency, effectiveness, and compliance

Maintain awareness of ISO standards while developing solutions to satisfy business needs

Performs other duties assigned as needed.

Required Qualification and Core Competencies for the role:

Bachelor degree in engineering, scientific or quality and compliance disciplines. Will accept the equivalent relevant industry experience in the absence of a degree

At least 5 years experience in Quality (medical devices and validation of equipment preferred)

Recommended Lean six sigma Green/Black belt, Project Management Certification will be an asset for this position

Experience in regulated ISO 13485 industries

Excellent communications skills

Organizational skills, ability to resolve conflicts

Strong analytical thinking skills and the ability to work in a flexible way under time pressure in local and global teams

Ability to make risk based decisions under time pressure

Understands the business implications regarding quality positions and decisions

High sense of responsibility and reliability

Work independently within established timelines

Experience with ETQ, Windchill and Saleforce S&R system will be beneficial

Fluent in English

Ability to travel if and when required (5%-10%)

Demonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices, and has experience generating effective prompts to boost efficiency and productivity

EXPERIENCE AND EDUCATION

Bachelors degree in engineering or other technical field preferred.

Experience in Medical Device environment (2-5 years).

Recommended Lean six sigma Green/Black Belt, Project Management Certification or ASQ certification (CIA, CQE) are an asset for this position.

Experience in regulated ISO 13485 industries.

REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS

Excellent communications and analytical skills are required.

Ability to work in a team is required.

Organizational skills, ability to resolve conflicts.

Analytical/Problem solving skills.

High sense of responsibility and reliability.

Work independently within established timelines.

Experience with EtQ, Trackwise, and Salesforce are beneficial for this role.

Additional language skills are beneficial for this role.

"Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company,

operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months,

subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be

required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that,

following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by

DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be

provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes."

Required Skills:

Preferred Skills:

Business Savvy, Compliance Management, Continuous Improvement, Corrective and Preventive Action (CAPA), Developing Others, Fact-Based Decision Making, Give Feedback, Inclusive Leadership, ISO 9001, Leadership, Quality Control (QC), Quality Management Systems (QMS), Quality Processes, Quality Standards, Standard Operating Procedure (SOP), Team Management

The anticipated base pay range for this position is:

€64 000,00 - €103 040,00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Amersfoort, 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 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.