Global Regulatory Strategy Lead

Boehringer Ingelheim Pharma GmbH & Co. KG; Biberach an der Riß; On-site; EUR 120,000 - 150,000; Full time

Job summary

Boehringer Ingelheim is seeking a dynamic regulatory professional to provide global strategic regulatory guidance and leadership across the product lifecycle. The role leads the Regulatory Excellence Team (RET) and represents Global Regulatory Affairs (GRA) on the Evidence Team, coordinating with Brand & Evidence and Global Labelling for submissions and RoW strategies.

Ideal candidates hold an advanced degree in pharmacy, life sciences, or chemistry, with strong regulatory experience across

Qualifications

• Master's or PhD in pharmacy, life sciences, or chemistry.
• Desirable RAC or Master of Drug Regulatory Affairs.
• Experience across US/EU regulatory environments with IND, BLA/NDA, or MAA.

Responsibilities

• Develop global regulatory strategies across projects.
• Lead Regulatory Excellence Team (RET) and represent GRA on Evidence Team.
• Oversee regulatory submissions and RoW rollout planning.
• Mentor team members and manage regulatory risks.

Skills

Leadership

Global regulatory strategy

Cross-functional work

English proficiency

Strategic thinking

Education

Master's or Doctoral Degree in pharmacy, life sciences, or chemistry

Job description

OUR COMPANY

At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe that, if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve; after all, we started with just 28 people. Now, we are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture.

The Position

We are seeking a dynamic individual to provide global strategic regulatory guidance and leadership throughout the product lifecycle on assigned projects. In this pivotal role, you will develop and be accountable for the Global Regulatory Strategy of your projects lead the Regulatory Excellence Team (RET) and represent Global Regulatory Affairs (GRA) on the Evidence Team (aka the cross-functional project Team).

Tasks & responsibilities

• As a regulatory professional, you will contribute to a holistic global strategy for assigned Inflammation projects. Your leadership and in-depth expertise will enable you to interact seamlessly at all levels of the organization, drive project goals, and maintain the highest standards of professionalism, ethics, and regulatory compliance.
• You will lead the development and implementation of cutting-edge global strategic regulatory strategies. Your role will involve assessing regulatory risks, proposing innovative solutions, and collaborating closely with stakeholders to align regulatory strategies with business objectives.
• As the main GRA representative on the Evidence Team, you will ensure that regulatory considerations are incorporated timely and comprehensively in the decision-making process.
• You will lead the Regulatory Excellence Team (RET) for assigned projects, fostering a culture of excellence and continuous learning. Your role will involve mentoring team members, identifying training needs, and promoting a proactive and solution‑oriented approach.
• In collaboration with Brand & Evidence teams and Global Labelling, you will shape early target label profiles and oversee the planning, preparation, and execution of regulatory submissions. Your role will also involve supporting submission rollout for Rest of World (RoW) countries from a global strategic perspective.

Requirements

• High level of education in pharmacy, life sciences, or chemistry, ideally holding a Master's or Doctoral Degree. Additional certifications such as Specialized Pharmacist, Master of Drug Regulatory Affairs, or RAC are highly desirable
• In-depth knowledge of Regulatory Affairs across multiple regions, including the US and/or EU. You have a proven track record of developing and implementing successful regulatory strategies, ideally with preparation of IND, (s)BLA/(s)NDA and/or MAA, Health Authority meeting briefing documents and negotiating with Health Authority(ies) in a major market (e.g. US, EU)
• Regulatory experience in one or several of Boehringer Ingelheim's Therapeutic Areas is preferred, and experience outside of Regulatory Affairs, e.g. in Clinical Development and R&D will be considered a valuable asset
• Proven ability to interpret and translate complex scientific data and regulatory guidelines into project-specific proposals. You should have commercial awareness and a thorough understanding of the business environment
• Strong critical thinking and strategic mindset, with the ability to anticipate both opportunities and challenges in execution. You should excel at problem‑solving, decision‑making, and developing realistic action plans to achieve specific goals
• Excellent leadership, team management and communication skills, with the ability to influence, lead, and inspire cross‑functional teams. You should have strong interpersonal skills, relationship building, and conflict management skills, combined with excellent English skills

As part of our commitment to transparency and fairness, salary information will be shared during the recruitment process. We also offer a comprehensive benefits and wellbeing package.

Applications from persons with severe disabilities are warmly welcomed. In cases of equal qualifications, such applicants will be given preferential consideration in the selection process.

With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.

Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.

Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.

Want to learn more? Visit https://www.boehringer-ingelheim.com

Ready to contact us?

Do you have any questions about the job posting or the next steps? You can find everything you need to know about the application, hiring, and internal transfer process here. If you have any further questions, please contact our HR Direct Team, Tel: [phone] or via mail: [e-mail]