Within the framework of high-visibility R&D projects, we are looking for a profile specialized in
analytical R&D documentation management
to support complex and demanding scientific programs.
The environment is
fast-paced
, with a
high volume of data
and strategically critical deliverables.
Mission
You will be responsible for the
management and follow-up of strategic analytical R&D documentation
.
The documentation is
highly dynamic
:
* frequent updates
* continuous back-and-forth
* daily modifications
You will work on:
* data related to
complex biological products
* multiple comparative datasets
* structured tables integrating the
control strategy
Your role will include:
* identifying
critical points
within documentation
* ensuring follow-up of:
* testing protocols
* acceptance criteria
* comprehensive lists of performed tests
* ensuring
consistency, traceability, and reliability
of documentation
Tools
- Excel (data structuring and tracking)
- Regulated document management system (e.g. Veeva – experience is a plus)
What are we looking for?
Profile Sought
* Master's degree in a scientific field
* Background in:
* life sciences
* biochemistry
* chemistry
* Previous experience in the pharmaceutical or biotechnology industry
* large pharmaceutical groups or smaller innovative structures
* Experience in
R&D Quality Control applied to strategic documentation
* Pure Quality Assurance profiles are
not
targeted
Key Skills
* Highly
structured and detail-oriented
profile
* Strong
rigor and attention to detail
* Ability to analyze, question, and
challenge document consistency
* Comfortable working under pressure and handling large volumes of data
Languages
* French: mandatory
* English: mandatory (primary working language)