Advisor – Global Regulatory Affairs CMC Biologicals
Job in
7849, De Kiel, Drenthe, Netherlands
Listed on 2026-07-29
Listing for:
Elanco
Full Time
position Listed on 2026-07-29
Job specializations:
-
Pharmaceutical
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Healthcare
Job Description & How to Apply Below
Advisor – Global Regulatory Affairs CMC Biologicals
The purpose of the Advisor – Global Regulatory Affairs CMC Biologicals role is to work cross functionally with Elanco R&D, Manufacturing, Quality, and other Elanco departments in support of the authorization and maintenance of registrations with global regulatory agencies for the biological products.
The role also executes CMC regulatory functions necessary to support geo-expansion activities for currently registered veterinary biological products as well as new innovations in the biological space.
Responsibilities
Design/develop regulatory CMC strategy for post-approval changes and geo-expansion of marketed biological products with a focus on creativity and innovation, maximizing the business benefit balanced with regulatory compliance.
Maintain a positive collaboration and partnership with internal groups in R&D, Manufacturing, Quality, and global regulatory business partners of Elanco.
Lead CMC regulatory pre-submission preparation and proactively communicate CMC regulatory strategy, key issues and other critical topics throughout the product life cycle to interdisciplinary project teams, while applying the global strategy into submissions.
Ensure that the required documentation and any content and/or timelines for global submissions are communicated to the appropriate teams and tracked according to the functional procedures.
Author high-quality CMC regulatory documentation for submission, applying global regulatory CMC strategies while assuring regulatory compliance.
Stay abreast of changing regulatory guidelines and requirements or industry technical trends and proactively share the information within the organization.
Minimum Qualifications
Bachelor of Science
Excellent understanding of EU regulatory legislation for veterinary vaccines
Fluent in English and German
8+ years in Global Regulatory Affairs, preferably within vaccines, biotechnology, CMC, etc.
Experience in developing regulatory CMC strategy for Europe (EMA) and most of the world countries is preferred.
Excellent communication skills including scientific writing.
Strong planning and organizational skills.
Flexibility and adaptability to leverage new technologies.
Ability to work cross-functionally and influence decisions in a matrix environment.
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
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