Johnson & Johnson Posted October 6, 2026

Commercial Quality Senior Specialist

Warsaw, Poland Full time
Quality Senior
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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:

Professional

All Job Posting Locations:

Warsaw, Masovian, Poland

Job Description:

We are searching for the best talent for a Commercial Quality Senior Specialist.

Purpose

We are looking for a Commercial Quality Senior Specialist to join our team at the Johnson & Johnson Distribution Center in Warsaw, Poland.

In this role, you will partner with Quality and cross-functional teams to help ensure processes operating under the Quality Management System remain compliant with Johnson & Johnson standards and applicable local regulatory requirements. You will contribute to maintaining and improving quality processes across distribution, storage, repackaging, relabeling, documentation, training, and supplier-related activities.

Working closely with local and global stakeholders, you will help drive compliance, support quality system activities, and contribute to the continuous improvement of quality processes across the Distribution Center.

You will be responsible for

In this role, you will provide Quality support for Distribution Center activities and contribute to the effective operation of the Quality Management System. You will work across multiple quality processes to help ensure products, documentation, and operational activities are managed in accordance with regulatory requirements and company standards.

Key responsibilities include:

Providing Quality support for activities related to the storage and distribution of medical devices

Providing Quality support for medical device repackaging and relabeling activities, including release of repacked and relabeled products

Supporting Environmental Controls, Validation, Calibration, and Maintenance activities

Managing quality documentation, including document updates, distribution, archiving, periodic reviews, and controlled copies

Supporting training management activities and quality agreements associated with processes governed by the Quality Management System

Participating in the implementation of corporate quality standards and procedures, including compliance assessments

Supporting CAPA, non-conformance, quality investigation, change control, project, supplier qualification, risk management, and quality metric activities in accordance with Quality Management System requirements

Participating in audit preparation activities and supporting internal and external audits

Contributing to quality projects, implementation of new digital tools, and continuous improvement initiatives

Collaborating with local and global Johnson & Johnson departments to support quality and compliance objectives

The role contributes to identifying quality issues, supporting root cause analysis activities, and helping implement corrective and preventive actions that strengthen the effectiveness of the Quality Management System.

Qualifications / Requirements

We are looking for someone who combines quality and compliance knowledge with strong collaboration, organizational, and analytical skills.

Education & Experience

Master’s degree in a relevant discipline

Experience in a similar quality, compliance, pharmaceutical, medical device, or regulated environment

Experience working within a Quality Management System is preferred

Knowledge & Skills

Knowledge of applicable quality and regulatory requirements

Understanding of Quality Management Systems and quality processes

Experience using quality tools and electronic quality systems

Strong communication skills and ability to work effectively across teams

Advanced English language skills

Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint

Strong organizational skills, reliability, and attention to detail

Analytical and interpersonal skills

Ability to manage priorities effectively and work in a structured manner

Ability to work collaboratively within a team environment

Willingness to learn, take initiative, and contribute solutions

Demonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices, and uses effective prompting techniques to support efficiency and productivity

What we offer

We offer a collaborative environment where learning, innovation, and professional development are encouraged.

In this role, you will have the opportunity to work with both local and global teams, contribute to quality and compliance initiatives, and support products that make a meaningful difference for patients.

Our commitment to inclusion

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation is powered by bringing together people with different backgrounds, experiences, and perspectives.

We are proud to be an equal opportunity employer and welcome applications from qualified candidates of all backgrounds.

If you require a reasonable accommodation during the application, interview, or onboarding process, support is available. Please let us know how we can help.

#LI-Hybrid

Required Skills:

Preferred Skills:

Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment

The anticipated base pay range for this position is:

zł121 000,00 - zł194 350,00

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
Senior
Function
Quality
Therapeutic area
Not listed
Location
Warsaw, Poland
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 230 comparable Senior Quality roles across 59 biopharma companies.

230Comparable roles tracked
216Currently active
59Companies hiring similar roles
29Countries represented

Salary context

58 of 230 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 Quality Control Chemist, Senior (Data Review) Mid Shift · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Peer group range $66,560 – $208,845 (median $131,050)

Where these roles are based

Top locations among the 230 comparable roles

United States122
Ireland15
China10
India9
Singapore9
Spain8

+ 23 more countries

Seniority mix

230 of 230 peers have a known seniority level

Senior165
Associate Director35
Principal30

Therapeutic area mix

0 of 230 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
Sandoz Strykow, Poland Senior
Same function Same seniority Same country
60%similar
IQVIA Warsaw, Poland Senior
Same function Same seniority Same country
45%similar
AbbVie Annecy, Auvergne-Rhône-Alpes Senior
Same function Same seniority
45%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same seniority
45%similar
Mylan Teoranta Inverin, Ireland Senior
Same function Same seniority
45%similar
Regeneron Ireland Limerick, Ireland Senior
Same function Same seniority

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.

60%
Senior Specialist GQS
Sandoz · Strykow, Poland · Senior
Function Therapeutic area Seniority Country
45%
Sr. Quality Assurance Specialist
Gilead Sciences, Inc. · La Verne, United States · Senior
Function Therapeutic area Seniority Country
45%
Senior Quality Assurance Validation Specialist
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Senior
Function Therapeutic area Seniority Country
45%
Senior Validation Engineer
Amgen Singapore Manufacturing Pte. Ltd · Singapore Manufacturing, Singapore · 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.