Our client, a leading pharmaceutical company, is seeking a specialist to oversee the qualification and operational readiness of a new production facility. The role involves partnering with project stakeholders to establish robust quality oversight throughout the transition from design to routine manufacturing operations.
Apply below after reading through all the details and supporting information regarding this job opportunity.
You possess a Master’s degree in a scientific field.
You bring 8+ years of experience in
QA
oversight within a
GMP
manufacturing environment.
You have a proven track record in health authority inspections and the certification process for new manufacturing facilities.
You possess strong knowledge of
biopharmaceuticals
or
gene therapy
manufacturing processes.
You bring expertise in
GMP ,
CFR, and
Eudralex
regulations for biopharmaceutical manufacturing.
You're able to provide mature quality judgment and communicate effectively with senior stakeholders.
You are fluent in
English
and
French .
Nice to Have
Broad transversal QA experience across multiple domains. xphnsxz
Ability to adapt to evolving priorities in an inspection-driven environment.
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