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Drive quality with purpose. At Uriach, we ensure compliance with the highest regulatory standards while supporting business, innovation, and sustainability across our entire product portfolio — from pharmaceuticals and medical devices to cosmetics, personal care, and food supplements. Our goal? To protect consumer trust with a pragmatic, forward-thinking, and sustainable approach to quality.
Your Key Responsibilities :
As part of our Quality Assurance team, you’ll be the guardian of product integrity and regulatory compliance. Your mission is to ensure every batch that reaches the market meets our quality promise — and the expectations of health authorities and consumers alike. Responsibilities include :
- Ensuring compliance with GMP, GDP, ISO 13485, ISO 22716, ISO 22000, and applicable EU directives and regulations.
- Reviewing and approving batch documentation, Certificates of Analysis, and releasing batches per Marketing Authorization requirements. Updating SOPs, managing the Quality Manual, and coordinating Management Reviews.
- Overseeing market release and ensuring proper product distribution.
- Investigating non-conformities, leading CAPA implementation, and driving continuous improvement. Managing product complaints, assessing recovered units, and making final decisions on returns, recalls, or suspected counterfeits.
- Leading audits — both internal and with third-party manufacturers and service providers.
- Overseeing supplier qualification, contract manufacturing oversight, and ensuring compliance from APIs to finished goods.
- Implementing and maintaining the Food Safety Management System and evaluating its performance.
- Ensuring data integrity in SAP, from product masters to client records. Monitoring and reporting quality KPIs, and supporting company-wide training and upskilling on quality topics.
What We’re Looking For :
Experience in Quality Assurance within a related industry is valuable.University Degree is a plus.Proficient in English. Other European languages are a plus.Experience working with SAP and TRACKWISE (or other e-QMS platforms).That’s your opportunity if you are a :
Critical thinker with a sharp eye for detail — you catch what others might miss.Proactive problem solver — you don’t wait for things to break; you improve them before they do.Clear communicator, able to translate complex regulations into practical actions across teams.Collaboration champion — you thrive in cross-functional environments, building trust across departments and with external partners.Calm under pressure, with the ability to prioritize and deliver in high-stakes situations.Adaptable and open to change, ready to work in a dynamic, fast-paced, and evolving regulatory landscape.Ethically driven, with an unwavering commitment to product quality and patient safety.Don't tick every box? No worries — we believe potential, curiosity, and a growth mindset matter just as much as experience. Everything can be learned.
Apply now!
Seniority level : Entry level
Employment type : Full-time
Job function : Quality Assurance, Pharmaceutical Manufacturing
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