BioTalent is working with a leading pharmaceutical organisation to support the search for a Qualified Person (QP) with strong experience in GMP, batch certification, and pharmaceutical quality systems.
This role will offer you
- A pivotal QP position within a global organisation where you will work closely with the Site Quality Director.
- The chance to collaborate across departments including QA, production, and regulatory affairs
- The opportunity to shape and enhance quality and compliance processes
You will be responsible for
- Certifying or rejecting product batches in accordance with AMG and GMP guidelines
- Ensuring documentation and processes meet regulatory standards
- Leading investigations into quality issues and implementing effective CAPAs
- Supporting audits, inspections, and continuous improvement projects
- Reviewing complaints, PQRs, and SOPs, and contributing to training and change control initiatives
Key Requirements :
- Degree in Pharmacy or a relevant scientific field
- In-depth understanding of GMP and pharmaceutical regulations
- Experience in manufacturing, quality documentation, and compliance
Please apply / email your resume with your availability to (emailprotected) to have a confidential discussion about this opportunity.
BioTalent Ltd are acting as an employment agency in relation to this opportunity.
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Qualified Person Arbeitgeber: BioTalent
BioTalent ist ein hervorragender Arbeitgeber, der Ihnen die Möglichkeit bietet, in einer Schlüsselposition als Qualified Person innerhalb eines globalen Unternehmens zu arbeiten. Hier profitieren Sie von einer offenen und kollaborativen Unternehmenskultur, die den Austausch zwischen Abteilungen fördert und Ihnen zahlreiche Möglichkeiten zur beruflichen Weiterentwicklung bietet. Zudem erwartet Sie ein dynamisches Umfeld, in dem Sie aktiv zur Verbesserung von Qualitäts- und Compliance-Prozessen beitragen können.

Kontaktperson:
BioTalent HR Team