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European Medical Director information

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$13K

$232.4K

$357K

How much do european medical director jobs pay per year?

As of Jun 16, 2026, the average yearly pay for european medical director in the United States is $232,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $198,000.00 and $284,500.00 per year, depending on experience, location, and employer.

What does a European Medical Director do?

A European Medical Director oversees the medical and clinical aspects of a pharmaceutical or healthcare organization across Europe. Their responsibilities include ensuring compliance with European medical regulations, providing scientific and medical expertise, leading clinical development strategies, and supporting product launches. They often collaborate with cross-functional teams, engage with regulatory authorities, and provide guidance on medical affairs to ensure patient safety and effective use of medicines.

What is the difference between European Medical Director vs European Medical Advisor?

AspectEuropean Medical DirectorEuropean Medical Advisor
CredentialsMedical degree, often with leadership experienceMedical degree, often with specialized knowledge
Work EnvironmentStrategic leadership, overseeing medical teams and projectsProviding medical expertise, supporting clinical trials and product development
Employer & Industry UsagePharmaceutical companies, biotech firms, healthcare organizationsPharmaceutical companies, medical communications, clinical research

The European Medical Director typically holds a leadership role with strategic responsibilities, overseeing medical teams and ensuring compliance across projects. In contrast, the European Medical Advisor focuses on providing expert medical input to support clinical and product development activities. Both roles require medical credentials, but their scope and focus differ significantly.

How does a European Medical Director typically collaborate with cross-functional teams across different countries?

A European Medical Director frequently works with cross-functional teams, including regulatory affairs, clinical development, commercial, and pharmacovigilance, across multiple European countries. This collaboration often involves coordinating medical strategy, ensuring compliance with diverse local regulations, and providing scientific support for product launches. Effective communication and cultural awareness are key, as the Medical Director must align stakeholders from various backgrounds to achieve common objectives. Regular meetings, both virtual and in-person, are common to facilitate alignment and address region-specific challenges.

What are the key skills and qualifications needed to thrive as a European Medical Director, and why are they important?

To thrive as a European Medical Director, you need an advanced medical degree (MD or equivalent), extensive clinical experience, and a strong understanding of European healthcare regulations. Familiarity with pharmacovigilance systems, regulatory submission tools, and certifications such as board certification in a relevant specialty are typically required. Exceptional leadership, cross-cultural communication, and strategic decision-making skills make candidates excel in this role. These competencies are vital for ensuring regulatory compliance, effective team management, and successful execution of medical strategies across diverse European markets.
Infographic showing various European Medical Director job openings in the United States as of June 2026, with employment types broken down into 100% Part Time. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $232,369 per year, or $111.7 per hour.
Director, Regulatory Affairs Devices and Combination Products

Director, Regulatory Affairs Devices and Combination Products

AbbVie

Irvine, CA • On-site

$161K - $212K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago

AbbVie rating

8.8

Company rating: 8.8 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

11th of 71 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Director Regulatory Affairs, Device is responsible for combining knowledge of scientific, regulatory and business issues to support and drive strategy for regulatory submissions, including new applications and amendments, renewals, annual reports, supplements and variations. Has influence and responsibility and is a key leader and driver of regulatory policy and strategy. Influences the development and changes of regulations and guidance. Interfaces with outside regulatory agencies and trade associations and provides management with regulatory metrics and information. Individual may plan, direct, coordinate and control regulatory affairs activities related to products worldwide. May supervise others.
  • Leads a global RA Device team in developing regulatory strategies for both development-stage and marketed products delivered with injection devices.
  • May manage the content of global regulatory dossiers directly and reviews regulatory submissions to ensure effective data and strategy presentation to regulatory authorities.
  • Advises internal personnel on regulatory strategies including responding to regulatory information requests. Provides strategic regulatory advice to peers in RA, R&D, and Operations. Seeks internal and external expert advice and technical support when necessary.
  • Devises regulatory strategies for complicated scenarios (e.g., complex dosage form or multiple operational changes, aggressive timelines).
  • Develops (or advises their team on) strategies for Device agency meetings, manages preparation for agency meetings, and manages content of pre-meeting submissions. They or their team member serves as the point of contact for the regulatory agency meetings and leads Device discussion with health authorities.
  • Drives strategic change planning with Manufacturing Operations using a risk-based approach centered on assessment of potential impact to quality, safety or efficacy. Manages products and change control with an understanding of regulations and company policies and procedures. Analyzes and approves manufacturing change requests.
  • Represents RA Device on project teams such as the product development, Global Regulatory Product Teams and Operations brand teams, for assigned projects. Negotiates with and influences team members to maximize chances for first pass approval of regulatory submissions.
  • Provides oversight and strategic guidance for creation of white papers and policies to illustrate current regulatory thinking.
  • Designs initiatives to drive business efficiencies across the organization (within or outside of the regulatory groups). Identifies opportunities for process improvements, identifies/solicits solutions and drives for implementation. Ensures enterprise culture initiatives are implemented across RA Device.
  • Trains, develops and mentors individuals; includes formal supervisory responsibilities.
  • Provides leadership to organizational staff by communicating and providing guidance towards achieving department objectives. Identifies engagement needs and partners with stakeholders to implement action plans accordingly.

Qualifications
  • Required Education: Bachelor's degree in pharmacy, biology, chemistry, pharmacology, engineering or related subject
  • Preferred Education: Relevant advanced degree preferred. Certification a plus
  • Required Experience: 10 years device and combination product experience with 2-plus years demonstrated leadership.
  • Preferred Experience: 10-plus years device and combination product experience, including 7-plus years in regulatory affairs or 7-plus years in Discovery, R&D, or Manufacturing
  • Experience developing and implementing successful global regulatory strategies. Experience interfacing with Health Authority and working in complex and matrix environments.
  • Strong oral and written communication skills.
  • Note: Higher education may compensate for years of experience
  • Knowledge of the ISO/CE process and global product registration process. Experience with eCTD tools and EDMS applications.
  • Knowledge of global regulatory intelligence and policy to analyze external regulatory trends and internal compliance trends to drive proactive initiatives to ensure compliance for Device/Combination Products.
  • Understanding of device/combination product regulations [21 CFR Parts 3, 4, GCP, GLP, 210/211, 820 QSR (Design Control), European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP, technical standards, ISO 14155, eCTD Module 3, ISO/IEC 62366, device complaint handling/MDRs, human factors testing, device risk analysis (ISO 14971) and other global regulatory requirements for AbbVie devices and combination products.
  • Ability to travel up to [15] % of time

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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