Last updated 2026-07-05
17 QA Engineering Jobs in Barcelona, 56, Spain
Browse 17 QA Engineering jobs across Barcelona, 56, Spain. Listings are updated hourly and include salary data where available.
Market data for QA Engineering jobs in Barcelona, 56, Spain
Professionals focused on ensuring product quality, compliance, and process improvement across various engineering and manufacturing sectors.
Companies with current QA Engineering listings
| Company | Active jobs |
|---|---|
| AstraZeneca | 3 |
| Ipsen Pharma SA | 2 |
| Neuroelectrics Barcelona SLU | 2 |
| Aizon | 1 |
| Cencora | 1 |
| ES03 (FCRS = ES003) Sandoz Industrial Products, S.A. | 1 |
| GE Vernova | 1 |
QA Engineering jobs by schedule
| Schedule | Active jobs | Share |
|---|---|---|
| Full time | 17 | 100% |
QA Engineering jobs by seniority
Common QA Engineering job titles
QA Engineering jobs by listed location
| Location | Active jobs | Share |
|---|---|---|
| Barcelona, 56, Spain | 15 | 88% |
| Barberà del Vallès, 56, Spain | 1 | 6% |
| El Masnou, 56, Spain | 1 | 6% |
FAQ
- How many QA Engineering jobs are listed in Barcelona, 56, Spain?
- This page currently shows 17 QA Engineering jobs in Barcelona, 56, Spain.
- Which companies are hiring for QA Engineering roles in Barcelona, 56, Spain?
- Current listings include roles from AstraZeneca (3 jobs, 18%), Ipsen Pharma SA (2 jobs, 12%), Neuroelectrics Barcelona SLU (2 jobs, 12%), Aizon (1 job, 6%), and Cencora (1 job, 6%).
- What seniority levels are common for QA Engineering jobs in Barcelona, 56, Spain?
- The visible seniority mix includes Mid (8 jobs, 47%), Senior (7 jobs, 41%), and Entry (2 jobs, 12%).
- What work schedules are common for QA Engineering jobs in Barcelona, 56, Spain?
- The visible schedule mix includes Full time (17 jobs, 100%).
- What QA Engineering job titles are common in Barcelona, 56, Spain?
- Common titles include Associate Director, Patient Safety Scientist (1 job, 6%), Clinical Research Associate (1 job, 6%), Director Técnico de Distribución (GDP) (1 job, 6%), Director of Engineering (Medical Device) (1 job, 6%), and Global Development Associate Medical Director (1 job, 6%).
- What does this market snapshot include?
- Most visible listings are full-time (17 of 17). Mid-level roles account for 8 of 17 listings.
Related jobs
Snapshot updated 3hr, 4m ago
AstraZeneca
Jun 30- Reporting to senior leaders in Patient Safety and working shoulder-to-shoulder with Safety Physicians and PV Scientists, you will drive the…
- Cross-Functional Representation: Represent Patient Safety on project teams across development and marketed portfolios, shaping program stra…
More roles at AstraZeneca
QA Operations Technician - Temporal
- Data integrity and eCompliance Support exception investigations Review and approval of production, QC, and AS and T records MBR review…
- Your main risponsabilities will include: Oversight of all production and testing activities, ensures compliance with cGxP, incl.
Ipsen Pharma SA
Jun 23- Auditing Host/Coordinate audits/inspections Risk assesment Approximately 2-3 years in similar position Education / Certifications (essentia…
- Auditing Host/Coordinate audits/inspections Risk assesment Approximately 1-2 years in similar position Knowledge & Experience (preferred):…
More roles at Ipsen Pharma SA
Siegfried Barbera S.L.
Jun 15- Assist in finding creative, practical solutions to workplace safety challenges Review and evaluate changes in SHE's toxicological risk mana…
- Deep understanding of international regulatory frameworks and guidelines related to pharmaceutical manufacturing, health-based exposure lim…
Inbrain Neuroelectronics
Jun 12- Strong knowledge of the human factors engineering process for medical/ pharma devices , including planning, execution, analysis, and report…
- Your profile Main Responsibilities: Work closely with Product, Engineering, Clinical, Regulatory, and Quality teams to ensure human factors…
GE Vernova
Jun 11- Job Description The Lead Product Safety Engineer is responsible for evaluating design safety and ensuring potential personnel and environme…
- Essential Responsibilities Facilitate and support product safety risk assessments for new and existing (installed base equipment) units.
Aizon
Jun 10- Working closely with senior quality, validation, and delivery colleagues, you will help build and maintain the quality program that underpi…
- Nice to Have Exposure to Computer System Validation (CSV) / CSA and GAMP 5.
Director of Engineering (Medical Device)
- Medical device experience in regulated environments: design controls, risk management, V&V, and tight collaboration with RA/QA.
- Experience supporting EU MDR and/or FDA submissions — technical files, V&V, audit interactions.
More roles at Neuroelectrics Barcelona SLU
Cencora
Jun 8- Key Responsibilities: Ensure compliance with GDP regulations across all operations Maintain and improve quality assurance systems and SOPs…
- Degree in Pharmacy (mandatory) Experience in GDP / Quality Management / Logistics Strong knowledge of pharmaceutical regulations Advanced i…
PUIG, S.L.
May 21- Experience in supplier audits and quality tools (Root Cause Analysis, 8D, FMEA, Control Plans, Sampling Plans – ISO 2859, ISO22716,…
- We'd love to meet you if you have Experience: 3–5 years of experience in Supplier Quality, Quality Assurance, or Quality…
Head Compliance and Risk Management
- Build, lead, and develop a high-performing global Compliance & Risk Management team, fostering a culture of accountability, transparency, a…
- Lead compliance strategy for digital quality and GxP systems, including eQMS, LIMS, LMS, MES, SAP, TrackWise Digital, and related platforms…
Zimmer Biomet Spain S.L.U
Apr 29- You will be responsible for supporting the Quality Assurance & Regulatory Affairs function of Portugal by: ensuring compliance with the…
- How You'll Create Impact Quality Management System (QMS) Support implementation, development, maintenance, and improvement of the local QMS…
Siegfried El Masnou, S.A.
Apr 28- Experiencia previa: 2-3 años de experiencia en departamento de validaciones ((validación de fabricación, cleaning y procesos de esterilizac…
- Apoyar al responsable de validación en la elaboración de informes de KPI.