Associate Director, Regulatory Affairs, Europe Regulatory Policy & Intelligence

ABBVIE

Hoofddorp

On-site

EUR 110,000 - 165,000

Full time

35 hours ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

AbbVie in Europe seeks an Associate Director, Regulatory Policy & Intelligence to shape regulatory strategy across EU member states and align with AbbVie portfolio priorities. You will lead regional topics, assess policy developments, and influence internal policy positions in concert with RPI and R&D teams.

This role requires deep knowledge of European healthcare regulations, experience with trade associations, and the ability to translate complex policy insights into actionable guidance for

Qualifications

  • Policy experience in life science environment is required.
  • Experience with regulatory policy and intelligence in the pharmaceutical industry or at a health authority.
  • Ability to assimilate regulatory trends and communicate impact to internal stakeholders.
  • Strong communication skills to translate complex data into insights.

Responsibilities

  • Independently manages and leads regional topics in the regulatory policy and intelligence function.
  • Analyzes proposed policies with emphasis on communicating impact of trends.
  • Leads formation of corporate positions to share with trade associations.
  • Prepares and presents complex written and oral reports to Senior Management and external audiences.

Education

Degrees in Pharmacy, Chemistry, Biology, Relevant Master’s degree or PhD in a scientific, health, legal, or business discipline preferred.

Job description

Associate Director, Regulatory Affairs, Europe Regulatory Policy & Intelligence
  • Full-time
  • Workday Global Grade: 19

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.

Reporting the Head of Europe, Regulatory Policy & Intelligence.

Position Overview:

The Associate Director, Europe Regulatory Policy & Intelligence (RPI), will be a strong subject matter expert in regulatory policy and procedure, laws and regulations with a comprehensive understanding of how regulatory policy is shaped and developed within Europe, and the business context for R&D. Ability to assimilate policy trends in the European Union, and engage with impact, in the external environment is a key capability for this role. Policy experience in life science environment is required.

The role will address policy and intelligence assimilation, analysis of changes in the regulatory environment, development of policy positions and advocacy strategies to advance policy goals through internal and external collaboration. The individual will work closely with RA and cross functional colleagues to coordinate policies to ensure alignment with AbbVie portfolio priorities.

The Europe RPI Associate Director develops, and maintains relations with HAs, peer company, and industry trade associations regarding scientific and regulatory policies, guided by company priorities. The role involves leadership of the development of cross-functional, multidisciplinary team responses to HA consultations, with a focus on aligning with company positions and scientific rigor. Through the provision of intelligence insights, the Associate Director assists company to comply with scientific, ethical, statutory, quality, and business requirements.

  • Independently manages and leads regional topics in the regulatory policy and intelligence function. Defines scientific and regulatory policy initiatives within assigned areas. A high level of proactivity and business acumen is required.
  • Serves as policy subject expert based on in depth knowledge of key regulatory issue and scientific basis. Analyses proposed policies with clear emphasis on communicating impact of trends. Leads formation of corporate position to share with trade associations, ensuring cross functional alignment.
  • Prepares and presents complex written and oral reports to Senior Management and external audiences on scientific and regulatory topics. Exceptional communication skills are needed to translate complex data into high-value insights.
  • Effectively uses negotiation skills to resolve policy issues when unable to agree internally. Anticipates and communicates consequences of path chosen.
  • Serves as liaison to trade associations for management on scientific and regulatory issues.
  • Supports supervisor and Senior Management in discussions of complex policy topics at trade associations.
  • Contributes to regulatory product development strategy by responding to information requests and providing an analysis of the regulatory environment.
  • Conducts external outreach with regulators, peers, and trades. Creates and responds to opportunities to enhance AbbVie’s relationship by participating in policy-related meetings. Utilizes local network of pharma companies to obtain policy-related information.
  • Degrees in Pharmacy, Chemistry, Biology, Relevant Master’s degree or PhD in a scientific, health, legal, or business discipline preferred.
  • Proven experience with the pharmaceutical industry or with a health authority
  • Regulatory policy and intelligence experience, including experience with trade associations, either from work in the pharmaceutical industry or at a health authority.
  • Robust knowledge of healthcare regulations in support of drug development, including experience in interpretation.
  • Experience working in a complex and matrix environment with demonstrated ability to assimilate policy trends, propose policy solutions with capability to influence internally and externally.
  • Exceptional communication skills are needed to translate complex data into high-value insights.
  • Well-established regulatory network across European countries
  • Experience with both medicines and medical devices would be an advantag

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 applicants seeking a reasonable accommodation, click here to learn more:

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Associate Director, Regulatory Affairs, Europe Regulatory Policy & Intelligence
Associate Director, Regulatory Affairs, Europe Regulatory Policy & Intelligence

AbbVie Inc. • Hoofddorp

Hybrid
EUR 150,000 - 190,000
Europe Regulatory Policy & Intelligence Lead
Europe Regulatory Policy & Intelligence Lead

ABBVIE • Hoofddorp

On-site
EUR 110,000 - 165,000
Europe Regulatory Policy & Intelligence Lead
Europe Regulatory Policy & Intelligence Lead

AbbVie Inc. • Hoofddorp

Hybrid
EUR 150,000 - 190,000
Toxin Brand Manager
Toxin Brand Manager

AbbVie • Nederland

On-site
EUR 90,000 - 150,000
Paid time off
Medical insurance
Dental insurance
+2
Study Start-Up Specialist
Study Start-Up Specialist

AbbVie • Hoofddorp

Hybrid
EUR 50,000 - 75,000
Hybrid work model
Brand Manager (Supply Chain Planning)
Brand Manager (Supply Chain Planning)

AbbVie Inc. • Zwolle

Hybrid
EUR 90,000 - 130,000
Regulatory Affairs Associate Specialist
Regulatory Affairs Associate Specialist

Abacus Medicine Group • Alkmaar

Hybrid
EUR 55,000 - 75,000
Toxin Brand Manager
Toxin Brand Manager

AbbVie Inc. • Zwolle

On-site
EUR 90,000 - 130,000
AA Clinical Specialist
AA Clinical Specialist

Allergan Aesthetics, an AbbVie Company • Hoofddorp

On-site
EUR 55,000 - 75,000
Finance Development Program 2027
Finance Development Program 2027

Abbvie • Hoofddorp

On-site
EUR 36,000 - 48,000