NEW OPPORTUNITY – Corporate QA Specialist (Pharma)
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On-site | Sant Cugat (Barcelona)
Oxford Global Resources – Life Sciences Unit is supporting one of the fastest-growing pharmaceutical companies headquartered in Spain, recognized for its strong commitment to innovation and R&D excellence.
We are currently looking for an experienced QA Specialist to join as a consultant their Quality Assurance team on a long term project basis.
Role : QA Specialist – (GMP, GxP Quality Systems)
Location : Sant Cugat (on-site)
Start : ASAP | Full-time, long-term project
Experience : Minimum 3–4 years in a similar QA GMP role
Main Responsibilities
Reporting to the QA Manager, the role is responsible for ensuring compliance with our client's internal policies and applicable regulatory standards, including Pharmaceutical Quality System requirements, Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GVP), ISO 13485, MDR, and 21 CFR Part 210 & 211 GxP, within the assigned scope of responsibility.
* Execute the Corporate Quality Assurance Program across all applicable sites, ensuring alignment with the Corporate Pharmaceutical Quality System standards and supporting continuous improvement initiatives.
* Manage the documentation system within the assigned area, including verification of personnel training status and ensuring full traceability of training records.
* Support internal and external audits, as well as inspections conducted by health authorities, ensuring readiness and compliance.
* Lead and manage deviation investigations within the assigned area, including defining, implementing, and verifying the effectiveness of CAPAs (Corrective and Preventive Actions), and coordinating change control processes.
* Actively participate in training activities and initiatives aimed at strengthening and continuously improving the Pharmaceutical Quality System.
* Provide objective quality data on a regular basis and contribute to the preparation of reports related to quality performance indicators (KPIs) within the assigned scope. xkdbapo
Your Profile
* Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or similar
* 3–5 years of experience in QA
* Solid knowledge of ICH, GxP, EU GMP Annex 13
* Experience working closely with manufacturing, analytical, and regulatory teams
* Spanish required; English professional level
* Team player with attention to detail and problem-solving mindset
What's in it for you?
Join a highly dynamic team in a company with a strong pipeline and innovative product portfolio
Work on-site in Sant Cugat hibrid
Be part of a mission-driven, growth-oriented pharma company
Interested?
Apply now or reach out to our Life Sciences team at Oxford Global Resources to learn more:
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