Are you looking for an opportunity to develop your professional career in a CDMO Quality Control department?
The successful candidate will join 3PBiovian, in Navarra, Spain, as part of our Quality Control department.
The candidate will be responsible for:
* Planning, coordinating, and supervising the work team involved in the follow-up of stability studies.
* Generating necessary documentation related to stability studies (protocols, reports, etc.).
* Reviewing stability study data records.
* Generating documentation related to reference materials (protocols, reports, certificates, etc.).
* Monitoring compliance of reference material analyses and reviewing stability study data records.
* Creating and reviewing raw material specifications.
* Approving the status of materials for manufacturing.
* Reviewing pharmacopoeia updates.
* Managing technical contracts with subcontracted companies and overseeing analytical subcontracting with external laboratories.
* Coordinating and planning daily activities of Physico-Chemistry and Biology laboratories.
Assessment criteria:
* University degree or equivalent in Biotechnology, Biochemistry, Biology, Chemistry, or related fields.
* Master's degree in Chemistry, Biotechnology, Biochemistry, Biology, or related fields.
* Proficiency in English (Level C1 / Advanced Certificate).
Minimum experience:
* At least 4 years in molecular biology and physico-chemical techniques specific to protein characterization.
* Experience with recombinant proteins, mAbs, biosimilars, ADCs.
* Knowledge of pharmaceutical regulatory guidelines.
We offer a flexible compensation plan, allowing employees to allocate up to 30% of their gross annual salary to tax-exempt services such as childcare, health insurance, and academic training.
Our benefits club provides exclusive discounts on various products and services, including Booking, FNAC, Rituals, and El Corte Inglés.
Relocation assistance is provided for new hires residing outside Navarra.
..And much more!
We recognize that passionate people with a shared purpose are essential to manufacturing advanced medicines.
We specialize in process development and cGMP manufacturing of biologics and cell therapy products, supporting clients through every stage from development to commercial production, with a focus on biotechnology applications in human and animal health sectors.
From development to product delivery, we are committed to supporting your biologics journey. As a leading global CDMO and preferred partner for pharmaceutical and biotech companies, we have the expertise to help improve lives.
It´s within us.
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