Giulia Paggiola
Regulatory Consultant (subcontractor) at MD Compliance Ltd | Zurich, Zurich, Switzerland
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Giulia Paggiola is a highly skilled Regulatory Consultant at MD Compliance Ltd, where she plays a pivotal role in guiding clients through the complex landscape of life science regulations. Leveraging over 13 years of industry experience, Giulia specializes in product lifecycle compliance, quality assurance, safety, security, and sustainability, ensuring that innovative medical devices, pharmaceuticals, and digital health solutions meet stringent regulatory standards. Her current role involves providing comprehensive QARACA (Quality, Regulatory, and Compliance Advisory) services to a diverse portfolio of international clients, including startups and established companies navigating the evolving regulatory environment.
At MD Compliance Ltd, Giulia leads strategic initiatives related to regulatory liaison, compliance system implementation, and risk management, with particular expertise in medical software development, drug-device combination products, and borderline cosmetics. Her deep understanding of the Software Development Life Cycle (SDLC), PMCF (Post-Market Clinical Follow-up), and cyber security risks enables her to advise clients on maintaining compliance throughout product development and post-market phases. Giulia’s proficiency in industrial policy, chemical industry regulations, and organic synthesis further enhances her ability to address complex regulatory challenges across multiple sectors.
A confident communicator and passionate problem solver, Giulia excels at translating intricate regulatory requirements into practical solutions, fostering collaborative relationships with stakeholders. Her leadership in change management and her ability to navigate regulatory pathways for innovative products make her an invaluable asset to her clients. With her comprehensive expertise and proactive approach, Giulia continues to drive compliance excellence and support the successful market entry and lifecycle management of life science products worldwide.
Regulatory Consultant (subcontractor) at MD Compliance Ltd in October 2018 to Present
Director Quality Regulatory Clinical Affairs at Medyria in May 2024 to Present
Head of Quality & Regulatory Affairs at Clue by Biowink in September 2021 to February 2024
Senior Regulatory and Compliance Manager at Clue by Biowink in August 2020 to September 2021
Regulatory Consultant at Hanway Associates in July 2018 to June 2020
Regulatory and Clinical Affairs Manager at Cognetivity Neurosciences Ltd in October 2017 to September 2018
Program Coordinator at GSK in January 2017 to September 2017
Senior Scientist at GSK in January 2016 to December 2016
Doctoral Researcher at University of York in October 2012 to September 2015
Founder & President at GreenSTEMS - Cross-disciplinary science community in July 2014 to July 2015
Intern - Analytical Quality Control at CatSci Ltd in September 2013 to December 2013
Intern - Corporate Social Responsibility at Procter & Gamble in June 2012 to September 2012
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University of York, Doctor of Philosophy - PhD, August 2026
University of York, Master's Degree, August 2026
Università degli Studi di Modena e Reggio Emilia, Bachelor of Science (BSc), August 2026
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Attention to Detail
Interpersonal Skills
Environmental, Social, and Governance (ESG)
Enzyme Kinetics
Reaction Kinetics
Statistical Data Analysis
Statistics
Healthcare Information Technology (HIT)
Collaborative Leadership
Stakeholder Engagement
Project Coordination
Drug Development
Drug Discovery
Product Lifecycle Management
Scientific Communications
Scientific Analysis
Scientific Reports
Technical Data Analysis
MHRA
Corrective and Preventive Action (CAPA)
Training
Consulting
Strategic Consulting
Quality System
Collaborative Problem Solving
Cross-team Collaboration
Software Quality Assurance
Training Delivery
Digital Health
Mobile Applications
Software Development Life Cycle (SDLC)
ISO 13485
ISO 27001
IEC 62304
ISO 14155
PMCF
Clinical Evaluation
Change Management
Start-up Consulting
Good Clinical Practice (GCP)
Good Manufacturing Practice (GMP)
Cosmetics Regulations
Narcotics Regulations
Good Laboratory Practice (GLP)
Marketing Strategy
Market Research
PRRC
Team Leadership
Clinical Trials
Regulatory Strategy Development
Supply Chain Management
Regulatory Compliance
Cyber Security Risk
Risk Management
Class III Medical Devices
U.S. Food and Drug Administration (FDA)
CE marking
Agile Project Management
Problem Solving
Teamwork
Artificial Intelligence (AI)
Medical Software
Medical Technology
Regulatory Affairs
Quality Management
Team Management
Culture Change
Organizational Culture
Public Speaking
Sustainability
Chemistry
Green Chemistry
Pharmaceutical Industry
Leadership
Public Relations
Project Management
Presentations
Sustainable Development
Science Communication
Chemicals Regulation
Solvent
Industrial Policy
Group Work
Blogging
Networking
Chemical Industry
Team Building
Biocatalysis
Renewable Resources
Organic Synthesis
Organic Chemistry
Research and Development (R&D)
Science
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What is Giulia Paggiola email address?
Email Giulia Paggiola at [email protected], [email protected] and [email protected]. This email is the most updated Giulia Paggiola's email found in 2026.
What is Giulia Paggiola phone number?
Giulia Paggiola phone number is +443344668899.
How to contact Giulia Paggiola?
To contact Giulia Paggiola send an email to [email protected], [email protected] or [email protected]. If you want to call Giulia Paggiola try calling on +443344668899. (updated on April 10, 2025)
What company does Giulia Paggiola work for?
Giulia Paggiola works for MD Compliance Ltd
What is Giulia Paggiola's role at MD Compliance Ltd?
Giulia Paggiola is Regulatory Consultant (subcontractor)
What industry does Giulia Paggiola work in?
Giulia Paggiola works in the Medical Devices industry.
Giulia Paggiola Email Addresses
Giulia Paggiola Phone Numbers
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