Regulatory Site Officer

Stellenbezeichnung: Regulatory Site Officer (all genders) - 2-year fixed-term contract
Location: Frankfurt

Regulatory Site Officer (all genders) - 2-year fixed-term contract page is loaded## Regulatory Site Officer (all genders) - 2-year fixed-term contract locations:
Frankfurt am Maintime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
February 14, 2026 (13 days left to apply) job requisition :
R2838400#
** About the job
**** Our Team:
**** About Sanofi:
** We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
*
* Main responsibilities:

*** Ensure regulatory compliance by assessing whether manufacturing and control procedures on site are in line with dossiers approved by Health Authorities
* Assessment of and decision on regulatory impact of product-related changes
* Manage regulatory site activities for changes with regulatory impact by organization of site meetings and participation in global meetings
* Support QA functions for implementation of changes by cross-functional communication of regulatory timelines and approval statuses worldwide
* Provides regulatory expertise to site projects like the introduction of new products, process technologies and continuous improvement projects
* Support change management of transfer projects by providing regulatory expertise for available product dossiers
* Write CMC regulatory documents/dossiers ready for submission by transforming scientific content to consistent CMC language and optimized terminology to facilitate the management of future changes
* Support Marketing Authorizations worldwide (territory extensions, renewals, site registrations and transfers, new submissions) by providing CMC documents/dossiers and collecting GMP related documents from the site(s)
* Coordinate and follow up submission-related regulatory requests following dossier variations or new registrations
* Prepare with contribution of site experts answers to questions from Health Authorities
* Act as interface to Global or Affiliate Regulatory Affairs for QA or Manufacturing functions of the site
* Collaborate in creation and maintenance of standard operation procedures with regulatory context
* Contribute to and support continuous improvement of performance and efficiency of regulatory working processes
* Support preparation of inspections and audits and participate as subject matter expert in audits/inspections
* Apply and optimize the use of appropriate company software tools to manage all regulatory activities#
** About you**
* ** Experience**:
Technical pharmaceutical CMC experience (laboratory, manufacturing, analytical control etc.) is desirable. Typically, at least 1-5 years of direct Regulatory CMC experience is preferred. Knowledge of global regulations/guidelines and key Health Authority and Industry trends of advantage.
* ** Soft skills**:
Capability of strategic thinking for resolving technical and regulatory issues. Demonstrate initiative, independent thinking, anticipatory foresight, and ability to communicate effectively to internal and external audiences. Ability to make decisions in a highly moving environment.
* ** Technical skills**:
Knowledge of both Chemical and Biological products is a plus. Skills for handling of internal data management systems and documentation tools.
* ** Education**:
Ph.D or Master in a science/health field (e.g. Chemistry, Pharmacy, Pharmacology, Biology, Biotechnology etc.) or equivalent.
* ** Languages**:
Fluency (oral and written) in German and English language is strongly recommended.
* Bring the miracles of science to life alongside a supportive, future-focused team.
* Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
* Benefit from a well-thought-out benefits package that rewards your contribution and commitment.
* Start your career at an attractive location in the center of Germany and experience our modern working environment and benefit from hybrid, flexible working time models.# Pursue
* progress*, discover
* extraordinary*Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our  and check out our Diversity Equity and Inclusion actions at !
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