8 Quality Engineering jobs in Milan.

Hiring now: Regulatory Affairs Mgr Cm @ Parexel, Tender Office Spec @ Baxter, Final Reviewer Certificat @ Sgs, Sr Implementation Consult @ Veeva Syst.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Affairs (3) CMC (3) Technical Documentation (3) Life Sciences (2) Submission Strategies (2) Project Management (2) Collaboration (2) Pharmacovigilance (2) Biopharmaceuticals (1) Quality Assurance (1)

📍 Locations

Milan (8)
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Parexel

Regulatory Affairs Manager - CMC biologics Milan
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.
Regulatory Affairs Manager - CMC biologics Milan
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

Tender Office Specialist Milan
Skills & Focus: Medical Devices, Tender Office Specialist, Quality Engineer, Sales, Customer Support, Clinical Education, Supply Chain, Patient Care, Innovation, Healthcare
About the Company: Baxter is a leading global medical products and services company that develops, manufactures, and markets a range of medical devices and therapies.
Type: Full time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.

Sgs

Final Reviewer & Certification Decision Maker Milan
Skills & Focus: Final Review, Certification Decision, Compliance, Audit Pack, Medical Device Regulations, QMS Audit, Technical Documentation, MDD, MDR, ISO13485
About the Company: SGS is a leading inspection, verification, testing and certification company.

Parexel

Local Qualified Person for Pharmacovigilance (QPPV) Freelancer Milan
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

Veeva Systems

Senior Implementation Consultant – Pharmacovigilance / Safety Systems Milan
Skills & Focus: Implementation, Pharmacovigilance, Safety Systems, SaaS, Consultant, Project Manager, Solution Architect, Life Sciences, Drug Safety, Customer Success
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: At least 5 years of working experience in life sciences industry with the majority spent in Drug Safety, Pharmacovigilance, Healthcare, or adjacent Safety Industry.
Type: Full-time
Benefits: 1% Veeva Giving program annual support for the non-profit(s) of choice, competitive benefits for employees.

Parexel

Regulatory Affairs Manager - CMC biologics Milan
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

Sgs

Product Assessor Milan
Skills & Focus: Product Assessment, Cardiovascular Products, Soft Tissue Products, Technical File Reviews, European Medical Device Regulation, Medical Device Directive, UKCA, CE Marking, Risk Minimization, Training Materials