Regulatory Affairs Manager

Valencia

Spain

Legal, Compliance, Regulatory Affairs, Corporate Security

As part of our dynamic team, you will take on a global regulatory and scientific affairs responsibility for ADM H&W pharmaceutical products, with a focus on EMEA oversight for microbiome-based food supplements and health-regulated ingredients. You’ll play a critical role in ensuring safety, efficacy, regulatory compliance, and market approval of our products, while driving business growth through proactive risk management and cross-functional collaboration.

Key Responsibilities:

- Pharma Regulatory Leadership: Define and implement regulatory initiatives for pharmaceutical approvals in line with global, regional, and national laws.
- Dossier Development: Manage and coordinate regulatory dossier submissions to secure and maintain product approvals and renewals.
- Pharmacovigilance: Oversee safety monitoring of approved and marketed products.
- Regulatory Strategy: Develop and implement strategies that align with commercial goals, enabling market access and innovation.
- Industry Representation: Represent ADM in industry organizations, regulatory bodies, and advocacy groups to influence evolving regulatory positions.
- Cross-Functional Collaboration: Work closely with internal teams to integrate commercial and brand plans into regulatory strategies.
- Continuous Improvement: Drive optimization of regulatory processes, systems, and delivery to internal and external stakeholders.
- Leadership & Coaching: Provide guidance within the H&W regulatory team to foster consistency, efficiency, and excellence.

What We’re Looking For:
Qualifications:

- Master’s degree in Pharmacy, Nutrition, Biotechnology, or a related field (PhD is a plus).

**Experience**:

- 7+ years in regulatory affairs within pharmaceuticals, food supplements, health ingredients, or related sectors.
- Global Expertise: Multi-market regulatory experience, with strong knowledge of EMEA frameworks (EMA, EFSA, FSA, MHRA, etc.).
- Technical Skills: Proven experience managing complex regulatory submissions (EU DCPs, RUPs, national registrations) and hands-on experience with regulatory systems and documentation platforms.
- Advocacy & Representation: Experience in regulatory advocacy and industry representation is desirable.
- Languages: Fluent in English (Spanish preferred).
- Soft Skills: Strategic thinker with excellent organizational, communication, and cross-functional collaboration skills.

Why Join Us?
At ADM, you’ll be part of a global team dedicated to making a difference in the health and wellness industry. We offer a collaborative environment, opportunities for professional growth, and the chance to contribute to innovative solutions that improve lives worldwide.

How to Apply:
Join ADM Health & Wellness - Where Science Meets Innovation

**#IncludingYou**

Diversity, equity, inclusion and belonging are cornerstones of ADM’s efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments — environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together.

For more information regarding our efforts to advance Diversity, Equity, Inclusion & Belonging, please visit our website here: Diversity, Equity and Inclusion | ADM.

**About ADM**

**Req/Job ID**

99898BR

LI-Hybrid

**Ref ID**

LI-MS1