Senior Regulatory Affairs CMC (ADC/Biologics)

Excelya Group; Saclay; On-site; EUR 90,000 - 130,000; Full time

Job summary

Excelya Group is seeking a senior regulatory consultant to provide strategic and operational Regulatory CMC leadership for a global Antibody-Drug Conjugate (ADC) biologics program. You will drive regulatory strategy, lead Module 3 CMC content, and coordinate with global health authorities to support MAAs, BLAs, and lifecycle management.

The role requires expertise in ICH, FDA, EMA regulations, and a proven ability to operate in a global matrix with cross-functional teams across development and

Qualifications

• Master’s degree or equivalent in a scientific discipline as listed.
• Solid experience leading regulatory CMC activities for biologics.
• Proven track record in MAA/BLA regulatory submissions and lifecycle management.
• Deep understanding of ICH, FDA and EMA requirements for Module 3.

Responsibilities

• Lead global Regulatory CMC strategy for biologics and ADC programs.
• Provide strategic leadership for BLA/MAA preparation, submission, and lifecycle management.
• Ensure alignment of CMC regs with development and commercial objectives.
• Anticipate regulatory risks and develop mitigation plans.
• Oversee Module 3 CMC content for global submissions.
• Coordinate interactions with health authorities (FDA, EMA).
• Drive cross-functional collaboration in a global matrix environment.
• Maintain expertise in international regulatory requirements for successful registrations.

Skills

Regulatory CMC leadership

Module 3 submissions

Global regulatory strategy

FDA/EMA knowledge

Cross-functional leadership

Regulatory submissions

Education

Master’s degree in Pharmacy, Chemistry, Life Sciences, Biotechnology, Pharmaceutical Sciences or related

Job description

Join Excelya, a dynamic and innovative company committed to excellence and collaboration in the field of translational research. Our global team of experts are the powerful force behind our success. When you work at Excelya, you become part of an international network that nurtures your talent, builds your skills and recognizes your value.

Our client is looking for a senior regulatory consultant to provide strategic and operational Regulatory CMC leadership support for a global Antibody-Drug Conjugate (ADC) biologics program. The selected consultant will play a critical role in leading global Regulatory CMC activities associated with Marketing Authorisation Applications (MAA) and/or Biologics License Applications (BLA), with a focus on global regulatory CMC strategy and matrix-management leadership.

Missions

• Lead and drive the global Regulatory CMC strategy for biologics and Antibody Drug Conjugate (ADC) programs.
• Provide strategic leadership for global BLA and MAA preparation, submission, and lifecycle management activities.
• Ensure alignment of CMC regulatory strategies with overall product development and commercialization objectives.
• Anticipate regulatory risks and develop proactive mitigation plans.
• Oversee the preparation, review, and finalization of Module 3 CMC content for global submissions.
• Ensure scientific consistency, regulatory compliance, and quality of submission documentation.
• Lead interactions with global health authorities, including FDA, EMA, and other international agencies, on CMC-related topics.
• Coordinate responses to regulatory questions, deficiency letters, and agency requests.
• Drive cross-functional collaboration within a global matrix environment, aligning regulatory, technical, and program teams.
• Maintain expertise in ICH, FDA, EMA, and international regulatory requirements to support successful registration and lifecycle management of biologic and ADC products.

About you !

Education : Master’s degree or equivalent in Pharmacy, Chemistry, Life Sciences, Biotechnology, Pharmaceutical Sciences or a related scientific discipline.

Experience : Solid experience in Regulatory CMC within the pharmaceutical industry, strong expertise in Biologics product

Skills : Proven hands-on experience leading Module 3 of biologic MAA and/or BLA submissions. Understanding of ICH, FDA, and EMA regulatory requirements applicable to Module 3.

Demonstrated experience defining and implementing global regulatory strategies.

Langages : Fluent English required

About Excelya

At Excelya, we combine a passion for science with a strong team spirit to redefine excellence in healthcare.

We are an ambitious healthcare company bringing together more than 900 employees across Europe, with the ambition of becoming the leading mid-sized CRO in Europe, while providing the best possible employee experience.

Our integrated service model, combining Consulting, Functional Service Provider (FSP), and Full-Service solutions, gives you the opportunity to work on a wide variety of high-value projects. You will collaborate with recognized experts and make a meaningful contribution to improving the patient journey.

At Excelya, caring is at the heart of everything we do. We promote equal opportunities and are committed to building a diverse, equitable, and inclusive working environment where everyone can thrive, be recognized, and fully contribute to a shared mission. Your challenges become our collective mission. Together, we turn ambitious ideas into tangible achievements, the Excelya way.