Johnson & Johnson Posted September 28, 2026

Associate Director, Evaluation and Quality Standards

Cornellà de Llobregat, Spain Full time
Quality Associate Director
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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:

Data Analytics & Computational Sciences

Job Sub Function:

Data Science

Job Category:

People Leader

All Job Posting Locations:

Cornellà de Llobregat, Barcelona, Spain, Madrid, Spain

Job Description:

Evaluation & Quality Standards to join our Data Science and Digital Health team (DSDH). This is a newly created leadership role within the Generative AI organization, reporting directly to the Head of Generative AI.

The GenAI team is deploying AI across discovery, development, regulatory, and operations to create AI assistants and agentic systems across the therapeutic areas and functions. As we scale from proof-of-concept to enterprise deployment, we need a dedicated evaluation function that defines what quality means for generative AI in a regulated pharmaceutical R&D environment, communicates the metrics effectively, and enforces that standard across every platform, vendor, and capability we build or adopt. This role owns evaluation and governance for all generative AI work across R&D.

Key Responsibilities

Evaluation Framework Design

•       Design and maintain evaluation frameworks for GenAI solutions spanning LLM quality, RAG performance, agent reliability, safety, and scientific accuracy.

•       Develop therapeutic-area-specific evaluation criteria with business teams, reflecting domain-specific quality requirements per therapeutic area and application type.

•       Define benchmarks for scientific validity, regulatory compliance, data quality, and operational reliability.

•       Establish gold-standard validation datasets and automated evaluation pipelines.

Vendor and Solution Assessment

•       Lead structured vendor assessments producing written Evaluation Reports

•       Challenge vendor claims with independent benchmarking; distinguish genuine capability from demonstration performance.

•       Assess integration complexity, total cost of ownership, regulatory posture, and vendor lock-in risk.

Governance and Standards

•       Serve as technical lead for the Evaluation & Standards Board, a cross-functional governance body for GenAI quality.

•       Present evaluation findings and recommendations to the GenAI Portfolio Steering Committee.

•       Define what “production-ready” means for GenAI in a regulated R&D environment and enforce that standard.

•       Set evaluation gates for product development stages: PoC, Limited Release, Scaled Product, and Product Ops.

Cross-Functional Collaboration

•       Partner with QMS/MLOps on the handoff from pre-adoption evaluation to production quality monitoring.

•       Work with therapeutic area teams on domain-specific evaluation standards.

•       Collaborate with Data Strategy & Products on data quality as an input to the evaluation rubric.

•       Engage JJIT architecture teams on platform-layer evaluation and security assessments.

Opinion Leadership and Capability Building

•       Contribute to the weekly GenAI Outlook newsletter, specifically the evaluation implications of frontier AI developments.

•       Build internal evaluation capability through training, documentation, and tooling for teams conducting assessments.

•       Publish evaluation standards and rubrics as reference material for the broader organization.

Team Leadership

•       Build and lead the GenAI Evaluation & Standards team

•       Attract, develop, and retain top talent in AI evaluation, quality science, and governance.

•       Establish a culture of scientific rigor and independent judgment within the team.

What This Role Is Not

•       Not MLOps or production monitoring: the QMS function handles post-deployment operations.

•       Not platform engineering.

•       Not regulatory affairs or medical writing.

•       Not vendor management or procurement: evaluation is independent of purchasing.

Key Qualifications

•       Advanced degree (PhD strongly preferred) in computational biology, bioinformatics, data science, computer science, AI/ML, biomedical engineering, applied mathematics, or related discipline.

•       Minimum 8 years of post-academic industry experience, with significant time in pharmaceutical or biotechnology R&D.

•       Hands-on expertise with generative AI systems: large language models, retrieval-augmented generation, agentic frameworks, and prompt engineering.

•       Demonstrated track record designing evaluation frameworks, scientific benchmarks, or quality standards for AI/ML systems.

•       Strong people leadership experience, including building and managing technical teams in a matrixed organization.

•       Excellent communication skills: ability to present complex technical findings clearly to non-technical senior stakeholders and defend unpopular conclusions.

•       Strategic thinking capability: ability to connect technical evaluation to business impact and organizational decision-making.

Required Skills:

Preferred Skills:

Advanced Analytics, Budget Management, Compliance Management, Critical Thinking, Data Analysis, Data Privacy Standards, Data Quality, Data Reporting, Data Savvy, Data Science, Data Visualization, Developing Others, Digital Fluency, Inclusive Leadership, Leadership, Program Management, Strategic Thinking, Succession Planning

The anticipated base pay range for this position is:

€75,000.00 - €129,260.00

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
Associate Director
Function
Quality
Therapeutic area
Not listed
Location
Cornellà de Llobregat, Spain
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 315 comparable Associate Director Quality roles across 83 biopharma companies.

315Comparable roles tracked
299Currently active
83Companies hiring similar roles
33Countries represented

Salary context

74 of 315 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 · Senior Quality Assurance Associate - 2nd Shift · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Peer group range $66,560 – $208,845 (median $159,000)

Where these roles are based

Top locations among the 315 comparable roles

United States133
China26
India21
Ireland19
Japan12
Singapore10

+ 27 more countries

Seniority mix

315 of 315 peers have a known seniority level

Manager160
Senior116
Associate Director39

Therapeutic area mix

0 of 315 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
Sandoz Madrid Delegación, Spain Senior
Same function Adjacent seniority Same country
50%similar
Moderna Biotech Spain S.L.U. Madrid, Spain Senior
Same function Adjacent seniority Same country
50%similar
Novartis Barcelona Provincial, Spain Senior
Same function Adjacent seniority Same country
50%similar
Johnson & Johnson Madrid, Spain Manager
Same function Adjacent seniority Same country
45%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority
45%similar
Novartis Indianapolis, United States Associate Director
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.

50%
Global Senior GMP Auditor
Sandoz · Madrid Delegación, Spain · Senior
Function Therapeutic area Adjacent seniority Country
50%
Senior Global GMP Quality Auditor
Novartis · Barcelona Provincial, Spain · Senior
Function Therapeutic area Adjacent seniority Country
45%
Site QC Head (Associate Director)
Novartis · Indianapolis, United States · Associate Director
Function Therapeutic area Seniority Country
45%
Associate Director - Quality Assurance - Device Assembly
Lilly · Pleasant Prairie, Wisconsin, United States of America · Associate Director
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.