13 Quality Engineering jobs in Madrid.

Hiring now: Global Gmp Sr Quality Aud @ Novartis, Quality And Compliance Le @ Iqvia, Regulatory Affairs Mgr Cm @ Parexel, Sr Dir Device Digital Saf @ Astrazenec, Final Reviewer Certificat @ Sgs, Sr Analyst Customs Trade @ Baxter.Explore more at jobswithgpt.com.

🔥 Skills

compliance (6) technical documentation (4) Regulatory Affairs (3) CMC (3) audits (2) training development (2) Submission Strategies (2) Technical Documentation (2) Project Management (2) Collaboration (2)

📍 Locations

Madrid (13)
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Novartis

Global GMP Senior Quality Auditor Madrid
Skills & Focus: GMP, audits, quality system, compliance, corrective action, manufacturing, risk-based assessments, audit strategy, training, regulatory guidance
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Type: Full-time

Iqvia

Quality and Compliance Lead (PharmaReview) Madrid
Skills & Focus: Quality compliance, pharmaceutical review, subject matter expert, training development, internal compliance, external regulations, quality control, audits, CAPA, risk evaluation
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3-5 years relevant experience in pharmaceutical review and/or compliance
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Regulatory Affairs Manager - CMC biologics Madrid
Skills & Focus: Regulatory Affairs, CMC, Life Sciences, Biopharmaceuticals, Quality Assurance, Submission Strategies, Technical Documentation, Project Management, Risk Mitigation, Collaboration
About the Company: Parexel is a global biopharmaceutical services organization that provides expertise and solutions to companies in the life sciences sector, helping them to nav…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, opportunities for career growth, and a supportive work environment.

Astrazeneca

Senior Director, Device & Digital Safety - CMO Madrid
Skills & Focus: digital, device development, patient safety, pharmacovigilance, regulatory compliance, collaboration, continuous improvement, team leadership, process improvement, strategic direction
About the Company: AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescriptio…
Experience: Extensive experience in pharmacovigilance and regulatory compliance within a pharmaceutical, clinical, regulatory or pharmacovigilance environment.
Type: Full time

Sgs

Final Reviewer & Certification Decision Maker Madrid
Skills & Focus: audit packs, compliance, MDR 2017/745, ISO13485, QMS, Certification Decision Maker, technical documentation, audit documentation, non-conformity, certificates
About the Company: SGS is a leading global inspection, verification, testing, and certification company, with a highly successful Global Medical Device team.

Parexel

Regulatory Affairs Manager - CMC biologics Madrid
Skills & Focus: Regulatory Affairs, CMC, Biologics, Pharmaceuticals, Submission Strategies, Quality Control, Risk Management, Project Management, Technical Documentation, Collaboration
About the Company: Parexel is a global biopharmaceutical services company that helps clients navigate the complex and ever-changing regulatory landscape.
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote/Office-based

Baxter

Senior Analyst – Customs & Trade Compliance, EMEA Madrid
Skills & Focus: customs, trade compliance, supply chain, analyst, EMEA, medical devices, healthcare, innovation, global, regulatory
About the Company: Baxter is a global leader in medical devices and solutions, focused on saving and sustaining lives through innovation in healthcare.
Type: Full time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.
Senior Analyst – Customs & Trade Compliance, EMEA Madrid
Skills & Focus: Customs, Trade, Compliance, EMEA, Supply Chain, Healthcare, Manufacturing, Innovation, Patient Care, Regulations
About the Company: Baxter is involved in improving patient care through high-quality products and innovative solutions in healthcare.
Type: Full time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.

Sgs

Senior Product Assessor - Active Devices Madrid
Skills & Focus: Product Assessor, technical documentation, EU regulations, compliance, Active Medical Devices, team management, cross-functional teams, KPI monitoring, recruitment, training development
About the Company: SGS is a global leader in inspection, verification, testing, and certification services.
Software & AI Product Assessor Madrid
Skills & Focus: technical documentation, SaMD, AI, Machine Learning, EU regulations, compliance, cross-functional teams, KPI’s, medical devices certification, service delivery
About the Company: Join our dynamic team at SGS and become a Software & AI Product Assessor. This role will allow you to make a significant impact in the field of certification.
Experience: strong background as a Product Assessor within an EU notified body conducting MDS technical documentation review

Baxter

Quality Associate I, Compliance Madrid
Skills & Focus: Quality, Compliance, Hospital, Products, Medical, Healthcare, Manufacturing, Regulatory, Testing, Engineering
About the Company: Baxter provides a broad portfolio of essential renal and hospital products, as well as a leading presence in the changing markets.
Type: Full time

Sgs

Final Reviewer & Certification Decision Maker Madrid
Skills & Focus: Final Reviewer, Certification, audit packs, compliance, MDD, MDR, ISO13485, technical documentation, QMS, decision-making

Parexel

Regulatory Affairs Manager - CMC biologics Madrid
Skills & Focus: Regulatory Affairs, CMC, biologics, clinical research, compliance, pharmaceuticals, project management, documentation, FDA regulations, biopharmaceuticals
About the Company: Parexel is a global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services.
Type: Full-time