Amgen S.A.S. Posted September 29, 2026

Director, Advisory Compliance H/F

Paris, France Full time
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About this opportunity

Career Category

Compliance

Job Description

JOIN AMGEN’S MISSION OF SERVING PATIENTS

At Amgen, if you feel like you are a part of something bigger, it’s because you are. Our shared mission, to serve patients living with serious illnesses, drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas – Oncology, Inflammation, General Medicine, and Rare Disease – we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Director, Advisory Compliance H/F

Based in France

What you will do

Let’s do this. Let’s change the world In this role, you will be at the forefront of shaping and advancing Amgen’s culture of ethics and integrity across France as part of ELMAC region as well as Amgen Global Corporate Functions as part of Worldwide Compliance and Business Ethics (WC&BE). Beyond ensuring adherence to healthcare compliance and privacy requirements, you will serve as a visible leader and trusted advisor, partnering with senior leadership, setting the tone for accountability, and embedding compliance as a core value in business decisions. You will strengthen the regional compliance program by championing a risk-based approach, navigating complex regulatory landscapes, and empowering teams to integrate ethics into daily operations.

In addition, you will hold strategic accountability for Compliance Data Analytics across region, including data usage strategy, governance, analytics capabilities, and predictive risk management, while supporting responsible use of data and technology in compliance.

By anticipating regulatory changes and aligning global standards with local needs, you will reinforce Amgen’s position as a trusted industry leader committed to doing business the right way.

Key Responsibilities

Leads and elevates the compliance strategic business partner role across a designated region, affiliate, business unit, or corporate function ensuring effective support for all business activities including Commercial, R&D, Government Relations, and Value & Access and Pricing and Pricing

Provides direct compliance support to Amgen executive leaders at the General Manager level and above

Directs and empowers the implementation and supports the oversight of comprehensive compliance and privacy programs, covering anti-corruption, anti-bribery, data privacy, and trade compliance across assigned region

Advises and influences business leadership and stakeholders on compliance strategy, interpretation of codes, legislation, and Amgen’s policies, serving as a single point of contact for regional leadership teams and providing region-specific guidance as needed

Uses deep industry and professional expertise and proven risk analysis skills to provide strategic compliance advice on the application of Amgen WC&BE standards and requirements to find innovative compliance solutions that meet the needs of the businesses we support

Partners cross-functionally with Legal, Regulatory, HR, Finance, and other teams to align compliance initiatives and resolve complex compliance issues

Drives proactive risk management by overseeing regional and local risk assessments, anticipating vulnerabilities, and implementing effective mitigation strategies that strengthen business resilience

Leads innovation in compliance by integrating and overseeing AI-driven compliance monitoring and analytics systems, leveraging advanced technologies to proactively identify, assess, and mitigate compliance risks across regions

Guides responsible AI use by advising on the ethical, regulatory, and privacy implications of AI deployment in business operations, ensuring alignment with evolving laws and industry standards

Supports investigations, incident management, and protocol adherence, collaborating with global and regional investigation teams, audit, and monitoring functions, ensuring compliance with local compliance requirements

Strengthens third party governance by leading distributor and third-party compliance oversight, ensuring due diligence and adherence to anti-bribery and anti-corruption and other regulatory requirements

Maintains up-to-date awareness of applicable laws, regulations, and industry codes, specific to designated region, monitoring changes and advising on necessary updates to compliance frameworks and strategies

Leads and participates in internal and external compliance forums, industry associations, working groups, and expert panels to exchange best practices and advance programs related to patient centricity, value-based healthcare, digital health, and ethical leadership

Inspires learning by developing, delivering, and evaluating impactful training programs and materials on compliance, privacy, and local codes, coordinating learning management systems and tracking participation

Drives alignment by reviewing, refining, commenting on, and implementing healthcare compliance procedures, policies, and training, ensuring alignment with SOPs and local codes

Owns the strategic Compliance Data Analytics agenda across region, including the data usage strategy, governance framework, analytics capabilities, and use of data and advanced analytics for predictive risk management; develops guidance and common approaches for Compliance Leads, drives adoption across the organization, and ensures alignment with regional counterparts

Guides responsible AI use in Compliance and the business by advising on the ethical, regulatory, privacy, and risk implications of AI deployment, and by supporting governance approaches that enable responsible adoption of emerging technologies

Leads continuous improvement through audit oversight, validation of corrective actions, and follow up activities for improvement actions to ensure accountability for enhanced program performance, coordinating regionally to address local findings

Data Privacy / CNIL: France represents a particularly complex and highly regulated privacy environment, reflecting the scale and nature of Amgen’s activities in the country and the extensive French data protection framework and CNIL requirements. The CNIL serves as Amgen’s lead supervisory authority in the EU. You will act as the Privacy Lead for France and the primary interface with CNIL for matters involving France, including matters with broader EU implications, providing senior, risk-based privacy guidance to the affiliate; supporting implementation of Amgen’s privacy requirements in the French context; and identifying and addressing privacy risks.

For cross-border privacy matters, including matters affecting countries beyond France, provides French-specific expertise and support to the Privacy Compliance and Digital Ethics team, while the EU Data Protection Officer / International Privacy Lead for ELMAC and JAPAC retains overall ownership of the international privacy framework and cross-border privacy matters. The France Compliance Director owns France-specific privacy accountability and the local CNIL relationship, in coordination with the EU Data Protection Officer and International Privacy Lead.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.

Basic Qualifications :

Doctorate degree and 4 years of experience in compliance, risk management, regulatory affairs, audit, law, or a related field

OR

Master’s degree and 8 years of experience in compliance, risk management, regulatory affairs, audit, law, or a related field

OR

Bachelor’s degree and 10 years of experience in compliance, risk management, regulatory affairs, audit, law, or a related field

AND

4 years of experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources

Preferred Qualifications:

In-depth knowledge of France and international healthcare compliance laws and standards (e.g., Anti-Kickback Statute, False Claims Act, Sunshine Act, GDPR) and other applicable standards

Familiarity with industry codes of conduct (e.g., PhRMA)

Strong understanding of compliance risk areas, including promotional practices, HCP interactions, and third-party oversight

Experience developing, implementing, and maintaining compliance policies, procedures, and training programs

Demonstrated ability to lead, coach, and manage teams across multiple regions and functions

Fluency in English and French

Comprehensive knowledge of privacy laws, healthcare regulatory matters, and anti-corruption laws applicable to the respective region

Demonstrated experience serving as a senior privacy advisor and/or interface with a data protection supervisory authority, with strong knowledge of French data protection requirements

Subject matter expertise in anti-bribery/anti-corruption (ABAC), prevention of off-label promotion, privacy, and transparency reporting

Ability to synthesize, analyze, and communicate complex compliance data and concepts to diverse audiences

Experience conducting and managing investigations, incident management, and remediation plans

Experience defining data usage strategies, governance frameworks, and analytics capabilities across a multi-country organization to strengthen predictive risk management

Skilled in leveraging AI and advanced analytics for compliance monitoring, risk assessment, and data-driven decision making

Knowledge of AI ethics, regulatory implications, and responsible use of emerging technologies in compliance

Self-starter with creative, strategic thinking and the ability to drive issues to closure in a fast-paced environment

Sensitivity to diverse groups, empathy, and ability to build meaningful connections with internal and external stakeholders

Ability to influence, negotiate, and resolve conflict

Ability to communicate with stakeholders at all levels, lead cross-functional teams, and drive results without direct authority

Good understanding of success in a matrix environment

THRIVE

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected gross pay range for this role in the posted location is visible on this page. Actual pay will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

APPLY NOW

Objects in your future are closer than they appear. Join us.

CAREERS.AMGEN.COM

EQUAL OPPORTUNITY STATEMENT

AMGEN is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

. Salary Range

124,901.55 EUR - 168,984.45 EUR

Job details

Seniority
Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Paris, France
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 82 comparable Director Regulatory Affairs roles across 36 biopharma companies.

82Comparable roles tracked
79Currently active
36Companies hiring similar roles
10Countries represented

Salary context

40 of 82 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Director, Regulatory Strategist · Mylan Inc. $112,000/yr – $236,000/yr
Peer group range $174,000 – $322,900 (median $254,075)

Where these roles are based

Top locations among the 82 comparable roles

United States58
Ireland8
United Kingdom7
Spain2
Japan2
Australia1

+ 4 more countries

Seniority mix

82 of 82 peers have a known seniority level

Director63
Senior Director16
Principal3

Therapeutic area mix

17 of 82 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology6
Rare Disease5
Neuroscience2
Cardiovascular / CVRM2
Vaccines & Infectious Disease2

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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45%similar
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

45%
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AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
45%
Director, RA Global Regulatory Strategy
AbbVie · Florham Park, NJ · Director
Function Therapeutic area Seniority Country
45%
Director, Regulatory Strategist
Mylan Inc. · Washington, United States · Director
Function Therapeutic area Seniority Country
45%
Director Regulatory Affairs Global CMC
McDermott Laboratories Limited · Northern Cross, Ireland · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.