Lilly Posted November 3, 2026

Ingeniero de Garantía de Calidad

Alcobendas, Madrid, Spain FULL_TIME
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Lilly 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 Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work, but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

DESCRIPCIÓN DEL PUESTO

Asegurar que los sistemas de calidad directamente relacionados con instalaciones, servicios, mantenimiento y equipos se gestionan de acuerdo con los estándares de calidad establecidos.

Asegurar que las instalaciones, servicios, equipos de fábrica y del Laboratorio de Control de Calidad con y sin automatización y sistemas de control distribuido se mantienen validados durante todo su ciclo de vida participando en los procesos de monitorización, revisiones periódicas y cambios en los mismos.

Colaborar en el mantenimiento del estado de validación/cualificación de equipos y de los procesos de empaquetado, bien a través de los controles de cambio que se produzcan o mediante las actividades de seguimiento establecidas en la estrategia de revisiones periódicas.

Participar en los equipos de gestión de proyectos y en las validaciones/cualificaciones de los mismos para asegurar que se realicen de acuerdo con los requerimientos establecidos por la Corporación para instalaciones, equipos y servicios.

Aprobar las revisiones periódicas o informes de monitorización del estado de cualificación de los equipos, instalaciones y servicios para garantizar su mejora continua.

Proporcionar consejo técnico y de calidad a las áreas de Mantenimiento e Ingeniería para conseguir mejora continua y asegurar excelencia funcional.

Asegurar que se realizan y documentan adecuadamente los mantenimientos preventivos y correctivos para garantizar la estabilidad del programa de mantenimiento.

Realizar la monitorización de los servicios para asegurar el cumplimiento de las especificaciones y realizar las evaluaciones periódicas de los mismos, así como la investigación de las desviaciones que se generen en dichos servicios.

Aprobar los documentos GMP de la planta para asegurar que cumplen con los estándares predeterminados, por ejemplo: procedimientos, especificaciones, validaciones, protocolos de cualificaciones, informes, etc.

Participar en las auditorías realizadas por las Autoridades Sanitarias, la Corporación o Terceros cuando sea aplicable.

REQUERIMIENTOS DE FORMACIÓN

Ingeniería preferiblemente Química o Industrial

REQUERIMIENTOS DE EXPERIENCIA

Experiencia mínima de 4 años en áreas de manufacturing y calidad en industria altamente regulada.

Se valorará positivamente experiencia en industria farmaceutica así como experiencia en procesos de cualificación y validación

REQUERIMIENTOS DE IDIOMA

Inglés fluído - hablado y escrito

HABILIDADES PERSONALES

Habilidades interpersonales: trabajo en equipo, orientación al cliente (interno/externo), toma de decisiones, buena comunicación oral y escrita.

Habilidades organizativas: cualidades para priorizar objetivos, personas muy organizadas y detallistas.

Habilidades técnicas: conocimiento en las normas de correcta fabricación, en conceptos de calidad y en su aplicación en la industria farmacéutica, así como mantenerse informado de las nuevas tendencias en instalaciones y servicios y su aplicación en la Industria Farmacéutica.

Manejo de herramientas informáticas: conocimientos de software ofimático de uso común a nivel usuario, así como conocimiento de los sistemas informáticos que controlan los procesos de negocio.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( https://careers.lilly.com/us/en/workplace-accommodation ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

€60,340 - €88,510

Full-time equivalent employees may also be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a pension plan; vacation benefits; eligibility for healthcare benefits; flexible benefits (if applicable) life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Alcobendas, Madrid, 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 1502 comparable Quality roles across 147 biopharma companies.

1502Comparable roles tracked
1357Currently active
147Companies hiring similar roles
54Countries represented

Salary context

261 of 1502 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 · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $123,250)

Where these roles are based

Top locations among the 1502 comparable roles

United States589
Ireland88
Germany72
China72
France67
India57

+ 48 more countries

Seniority mix

731 of 1502 peers have a known seniority level

Manager223
Senior189
Intern/Fellow/Postdoc98
Associate65
Director46
Associate Director45
Principal33
Senior Director25
Executive/VP7

Therapeutic area mix

3 of 1502 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2
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
Sandoz Madrid Delegación, Spain Senior
Same function Same country
40%similar
Moderna Biotech Spain S.L.U. Madrid, Spain Senior
Same function Same country
40%similar
Moderna Biotech Spain S.L.U. Madrid, Spain Associate
Same function Same country
40%similar
Moderna Biotech Spain S.L.U. Madrid, Spain
Same function Same country
40%similar
Moderna Biotech Spain S.L.U. Madrid, Spain Senior
Same function Same country
40%similar
Teva Pharmaceuticals Zaragoza, Spain
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.

Or follow a whole field: get every new Quality job in Spain, and choose locations and companies.

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%
Global Senior GMP Auditor
Sandoz · Madrid Delegación, Spain · Senior
Function Therapeutic area Seniority Country
40%
Sr. Specialist, Quality Control, Bioassay
Moderna Biotech Spain S.L.U. · Madrid, Spain · Senior
Function Therapeutic area Seniority Country
40%
Sr. Specialist, Quality Control, Chemistry
Moderna Biotech Spain S.L.U. · Madrid, Spain · Senior
Function Therapeutic area Seniority Country
40%
Specialist, Quality Control
Moderna Biotech Spain S.L.U. · Madrid, Spain · 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.