Johnson & Johnson Posted August 17, 2026

Analyst eLIMS CoE QC Operations

Schaffhausen, Switzerland Full time
Quality

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:

Quality Systems

Job Category:

Professional

All Job Posting Locations:

Horsham, Pennsylvania, United States of America, Leiden, South Holland, Netherlands, Malvern, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Ringaskiddy, Cork, Ireland, Schaffhausen, Switzerland

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent to join us as Analyst eLIMS CoE (QC Operations) at one of the following locations:

Schaffhausen, Switzerland

Leiden, South Holland, Netherlands

Ringaskiddy, Cork, Ireland

Horsham, Pennsylvania, United States of America

Malvern, Pennsylvania, United States of America

Raritan, New Jersey, United States of America

Why This Role Matters

This role offers you the opportunity to contribute to the future of digital QC laboratories by enabling compliant, reliable, and efficient eLIMS configurations across Johnson & Johnson’s global network. You will help strengthen standardization, support paperless laboratory workflows, and contribute to continuous improvement within a global Center of Excellence.

Purpose:

In this role, you will support the configuration, governance, and lifecycle management of complex master data within the eLIMS (LabVantage) system. You will ensure compliant, accurate, and standardized system configurations in a GxP environment that support QC Operations across a global network. As part of the eLIMS Center of Excellence, you will collaborate with laboratories, quality organizations, system owners, and cross-functional partners to enable efficient paperless laboratory processes, drive continuous improvement, and maintain regulatory compliance.

You will:

Create, review, approve, and maintain complex master data in eLIMS (LabVantage).

Ensure accuracy, completeness, compliance, and traceability of master data and related documentation.

Configure master data supporting Release, Stability, Raw Materials, Packaging Materials, and COA-related processes.

Support harmonized and standardized eLIMS configurations across multiple sites and processes.

Translate laboratory and business requirements into effective system configurations.

Execute and support change control activities, including impact assessments and implementation planning.

Support User Acceptance Testing (UAT), system upgrades, enhancements, and new implementations.

Drive continuous improvement initiatives and identify opportunities to optimize QC business processes.

Qualifications / Requirements:

Bachelor’s degree or equivalent combination of education and experience.

2 to 4 years of experience in a regulated environment.

Hands-on experience with eLIMS / LabVantage.

Solid knowledge of cGMP / GxP requirements, quality systems, compliance processes, and risk management principles.

Demonstrated ability to manage complex topics independently, prioritize effectively, and escalate appropriately.

Strong communication skills in English, minimum B2 level; C1 preferred.

Strong stakeholder management and cross-functional collaboration skills.

Ability to work independently and lead domain-specific initiatives.

Preferred Qualifications:

Advanced experience in eLIMS master data configuration across multiple data types.

Strong understanding of iLABs / paperless laboratory processes and New Product Introduction workflows.

Experience with Stability Master Data Management and COA configuration.

Experience with Enterprise Quality Systems such as COMET.

Experience in change control assessment and execution ownership.

Experience with EDMS solutions, for example TruVault.

Previous Johnson & Johnson experience is preferred.

Experience in the pharmaceutical industry is preferred.

Understanding of multi-site configurations across Biotherapeutics, Synthetics, and Advanced Therapies.

Core Competencies

Advanced analytical thinking.

High attention to detail.

Structured problem-solving.

Strong ownership and accountability.

Stakeholder influence and collaboration.

Ability to manage complexity in regulated environments.

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.

Here’s what you can expect:

Application review: We’ll carefully review your CV to see how your skills and experience align with the role.

Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.

Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.

Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.

Finally, at the end of the process, we’ll invite you to share feedback in a short survey. Your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process!

Netherlands – The anticipated base pay range for this position is 44.700 - 70.840 EUR

Ireland – The anticipated base pay range for this position is 42.400 - 67.965 EUR

#RPOEMEA

#LI-Hybrid

Required Skills:

Preferred Skills:

Analytical Reasoning, Business Alignment, Business Behavior, Collaboration, Communication, Compliance Management, Data Compilation, Data Quality, Data Savvy, Document Management, Execution Focus, Quality Auditing, Quality Control (QC), Quality Management Systems (QMS), Quality Services, Quality Standards, Systems Analysis, Training People

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Schaffhausen, Switzerland
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 909 comparable Quality roles across 103 biopharma companies.

909Comparable roles tracked
838Currently active
103Companies hiring similar roles
48Countries represented

Salary context

183 of 909 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 · Technician - QC Laboratory · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · AVP, External Quality · Merck $282,200/yr – $444,200/yr
Peer group range $43,753 – $363,200 (median $142,155)

Where these roles are based

Top locations among the 909 comparable roles

United States317
Ireland55
India51
Japan44
China44
Belgium39

+ 42 more countries

Seniority mix

428 of 909 peers have a known seniority level

Manager155
Senior132
Associate Director40
Director38
Associate27
Principal19
Senior Director11
Intern/Fellow/Postdoc4
Executive/VP2

Therapeutic area mix

1 of 909 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

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
Celgene International SaRL Boudry, Switzerland Associate
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40%similar
Novartis Basel (City), Switzerland
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Novartis Basel (Land), Switzerland
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40%similar
Novartis Schaftenau, Switzerland
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UCB Bulle, Gruyere, Switzerland
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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%
Associate Stability Scientist
Celgene International SaRL · Boudry, Switzerland · Associate
Function Therapeutic area Seniority Country
40%
TRD QA Global Sterility Assurance
Novartis · Schaftenau, Switzerland · Seniority not listed
Function Therapeutic area Seniority Country
40%
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UCB · Bulle, Gruyere, Switzerland · Seniority not listed
Function Therapeutic area Seniority Country
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RiSM Internship in GMP relevant functions for students in Pharmacy, Pharmaceutical Science or Pharmaceutical Technology (Basel, 6 months)
Roche · Basel, Basel-City, Switzerland · Seniority not listed
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.