21 Quality Engineering jobs in Paris.

Hiring now: Sr Mgr Drug Safety @ Biogen, Quality And Safety Dir @ Novo Nordi, Sr Technology Leader Adva @ Johnson Jo, Sr Safety Implementation @ Veeva Syst, Lead Qa Analyst @ Doctolib, Sr Implementation Consult @ Veeva, Local Qualified Person Fo @ Parexel, Quality And Regulatory Af @ Withings, Quality And Regulatory Af @ Impeto Med, Supply Chain Jobs @ Baxter.Explore more at jobswithgpt.com.

🔥 Skills

Pharmacovigilance (9) Quality Assurance (5) Project Management (4) ISO 13485 (4) compliance (3) Regulatory Compliance (3) Medical Devices (3) Safety (2) product development (2) Implementation (2)

đź“Ť Locations

Paris (9) Issy-les-Moulineaux (6) Châtillon (3) Puteaux (2) Guyancourt (1)
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Biogen

Sr. Manager, Drug Safety Puteaux
Skills & Focus: Pharmacovigilance, Biosimilars, Safety monitoring, Medical Information, Governance, Regulatory compliance, Audits and inspections, Data collection, Quality control, Training materials
About the Company: Biogen is a biotechnology company specializing in discovering, developing, and delivering innovative therapies for individuals living with serious neurological…
Experience: Senior level management experience in pharmacovigilance
Type: Full-time

Novo Nordisk

Quality and Safety Director Puteaux
Skills & Focus: Quality Management, Safety, Pharmaceutical Industry, Good Distribution Practices, Cross-functional Collaboration, Quality Assurance, Pharmacovigilance, Team Management, Employee Development, Legislation Surveillance
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. This includes a strong legacy …
Experience: 5-10 years in Quality Assurance and pharmacovigilance activities, 5-8 years in the pharmaceutical industry

Johnson & Johnson

Senior Technology Leader - Advanced Therapies Paris
Skills & Focus: technology leadership, supply chain, product development, cell therapy, gene therapy, program management, cross-functional, ERP, stakeholders, compliance
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 10+ years of experience in technology product management and/or technical program management
Type: Full-time

Veeva Systems

Senior Safety Implementation Consultant - Signal Detection and Analytics Paris
Skills & Focus: Drug Safety, Pharmacovigilance, Signal Detection, Implementation, Vault Safety, Project Management, Business Processes, Customer Success, Cross-functional Team, Regulations
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.
Experience: 5+ years of life sciences industry experience with majority spent in Drug Safety, Pharmacovigilance, Healthcare, or adjacent Safety Industry
Type: Full-time
Benefits: 1% Veeva Giving program to support non-profits of choice, work from home or in-office flexibility

Doctolib

Lead QA Analyst Paris
Skills & Focus: QA, Quality Assurance, Test Strategies, Automation Tools, Performance Testing, Regulatory Compliance, Leadership, Project Management, Mentorship, Cross-team Collaboration
About the Company: Join Doctolib's mission to transform healthcare by leading quality assurance initiatives across multiple teams.
Experience: 6+ years of QA experience
Benefits: Free Health Insurance for you & your family, Up to 14 days of RTT, Parental care program, Wellbeing program, Flexibilit…

Veeva Systems

Implementation Consultant – Pharmacovigilance / Safety Systems Paris
Skills & Focus: Pharmacovigilance, Implementation, Vault Safety, Project management, Gap analysis, Configuration, GxP software, SaaS solutions, Life Sciences, Customer training
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: At least 3+ years of experience in Life Sciences, Healthcare, or an adjacent Safety industry
Type: Full-time
Benefits: 1% of base salary annually for charitable causes, flexible work environment, employee equity program

Veeva

Senior Implementation Consultant – Pharmacovigilance / Safety Systems Paris
Skills & Focus: Pharmacovigilance, Safety, SaaS, implementation, consultant, project manager, solution architect, life sciences, drug safety, technology consulting
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: At least 5 years
Type: Full-time
Benefits: Work Anywhere policy, 1% Veeva Giving program, office workspace when working on-site

Parexel

Local Qualified Person for Pharmacovigilance (QPPV) Paris
Skills & Focus: Pharmacovigilance, Clinical Research, Remote Work, Safety Operations, Qualified Person, Freelancer, Data Management, Biostatistics, Clinical Trials, Regulatory Compliance
Type: Freelancer
Director, Qualified Persons Local Qualified Person for Pharmacovigilance (QPPV) Paris
Skills & Focus: Pharmacovigilance, Director, Remote, Clinical Trials, Biostatistics, Patient Inclusion, Drug Development, Quality Assurance, Global Operations, Collaborative Environment
About the Company: Parexel is a global biopharmaceutical services company. They focus on enhancing drug development and improving patient outcomes through innovation and technolo…
Local Qualified Person for Pharmacovigilance (QPPV) Freelancer Paris
Skills & Focus: Pharmacovigilance, QPPV, freelance, clinical trials, post-market, safety reporting, risk management, GVP, GCP, regulations
About the Company: Parexel is in the business of improving the world’s health. They provide a suite of biopharmaceutical services that help clients across the globe transform sci…
Experience: Minimum of at least 7 years' demonstrated experience in managing or implementing PV systems, including quality assurance experience.
Type: Freelance

Withings

Quality and Regulatory Affairs Specialist Issy-les-Moulineaux
Skills & Focus: regulatory affairs, quality management system, ISO 13485, medical devices, risk management, software development, MDR 2017/745, clinical studies, product lifecycle, compliance
About the Company: Withings is a pioneer and global leader in connected health, creating beautiful and intuitive products to help individuals take control of their health.
Experience: Minimum experience in a regulatory or technical role in the medical devices field, with a focus on medical software development.
Type: Full-time
Benefits: Stock Options, smartphone and computer of your choice, cultural and sports activity discounts, company restaurant, and …

Johnson & Johnson

Manager, Immunology Regulatory Medical Writing Issy-les-Moulineaux
Skills & Focus: Immunology, Regulatory, Medical Writing, Clinical Documents, Project Management, Cross-Functional, Team Leadership, Process Improvement, Pharmaceutical, Communications
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience.
Type: Full-time
Senior Regulatory Affairs Specialist - Shockwave Medical Issy-les-Moulineaux
Skills & Focus: Regulatory Affairs, Medical Devices, Advertising, Promotion, Compliance, Health Innovation, Product Claims, Stakeholder Engagement, Policy Development, Project Management
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Minimum 5 years in a regulated health industry; or 3 years with a Master’s degree; or a Ph.D. with 1 year of experience.
Type: Fully Remote

Impeto Medical

Quality and Regulatory Affairs Specialist Issy-les-Moulineaux
Skills & Focus: quality management system, regulatory requirements, ISO 13485, MDR 2017/745, product lifecycle, document control processes, CAPA, internal audits, medical device file, multidisciplinary interactions
About the Company: Impeto Medical specializes in innovative health solutions focusing on measuring and tracking physiological parameters. They develop advanced technologies to he…
Experience: 1 to 4 years in quality and regulatory functions within medical devices or healthcare.
Type: Full-time
Benefits: Stock Options, smartphone and computer of your choice, cultural and sports activity discounts, company restaurant, part…

Johnson & Johnson

Analyst II, Regulatory Medical Writing Issy-les-Moulineaux
Skills & Focus: Regulatory Medical Writing, clinical documents, protocols, clinical study reports, investigator’s brochures, quality control, literature searches, cross-functional teams, medical guidelines, pharmaceutical industry
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 2 years of relevant pharmaceutical/scientific experience is required.
Type: Full-time
Benefits: We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority,…

Withings

Quality and Regulatory Affairs Manager Issy-les-Moulineaux
Skills & Focus: Quality Management System (QMS), ISO 13485, regulatory compliance, medical device, continuous improvement, process management, document control, audits, medical device file, cross-functional communication
About the Company: Withings is a pioneer and global leader in connected health, known for creating beautiful and intuitive health products such as smart scales, hybrid watches, b…
Experience: 5 years in quality and/or regulatory functions in the health sector or heavily regulated environments; experience with medical devices is a plus.
Type: Full-time
Benefits: Stock Options, smartphone and laptop of choice, reductions for cultural and sporting activities, company restaurant, an…

Baxter

Supply Chain Jobs Guyancourt
Skills & Focus: Supply Chain, Customer Support, Sales, Marketing, Clinical Education, Healthcare, Medical Devices, Quality Assurance, Innovation, Diversity
About the Company: Baxter is dedicated to saving and sustaining lives by advancing healthcare solutions through innovation and quality.
Type: Full-time
Benefits: Comprehensive benefits options reflecting the value placed in employees.

Perrigo

Associate Computer System Validation (h/f) Châtillon
Skills & Focus: Computer system validation, Quality Assurance, GAMP 5, EU GMP Annex 11, FDA CFR Part 11, Data integrity, Quality Management System, ISO 9001, ISO 13485, Auditing
About the Company: Perrigo is a leading global provider of over-the-counter (OTC) health products and wellness solutions that enhance individual overall well-being. It is dedicat…
Experience: At least 2-5 years relevant experience in Computer system validation in Pharmaceutical and/or Medical Devices industry.
Type: Hybrid
Benefits: Competitive compensation and benefits package, opportunity to work in a hybrid working model, and career development op…
CMC Regulatory Affairs Project Manager Châtillon
Skills & Focus: CMC Regulatory Affairs, project management, healthcare products, medical devices, cosmetics, regulatory strategies, product development, quality management, technical documentation, compliance
About the Company: We are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the …
Experience: Minimum of 7 years of relevant work experience, preferably in CMC Regulatory Affairs or R&D.
Benefits: Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career dev…
Regulatory Affairs Associate Châtillon
Skills & Focus: Regulatory Affairs, Medicinal Products, Compliance, Product License Variations, EU Legislation, Quality, Submissions, Documentation Preparation, Regulatory Intelligence, Team Collaboration
About the Company: Perrigo is a top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula.
Experience: Minimum one year experience in a Regulatory environment
Benefits: Competitive compensation and benefits tailored to support employees and their families, along with career development o…