We are currently recruiting on behalf of our client in the
pharmaceutical industry
located in the
Neuchâtel area
. This is a
short-term assignment
for a
QA Expert
with a strong focus on
documentation systems
,
compliance
, and
continuous improvement
within a regulated environment.
Your Impact
* Own and manage documentation systems (e.g. Veeva Vault)
* Support users, resolve issues, and deliver training
* Create, update, and archive quality documents
* Help prepare for audits and inspections
* Drive improvements and collaborate across teams
* Back up other QA systems when needed
What You Bring
* Degree in life sciences, pharma, or related field
* 2+ years in the (bio)pharma industry
* Familiarity with GMP, GDocP, and regulatory standards
* Experience with document workflows and archiving
* Fluent in French and English
* Strong communication, organization, and problem-solving skills
Why Apply?
* Join a globally recognized pharmaceutical company
* Be part of a collaborative and international team
* Gain exposure to global QA processes and systems