Working in a CRO means ensuring that every pharmaceutical product meets the highest quality standards before reaching patients or clinical studies.

At Kymos Group, we are looking for a QA Scientist to join our QA Batch Release team. As a Scientist, you will play a key role in the batch certification and release process, ensuring that pharmaceutical products comply with GMP requirements, regulatory expectations, and quality standards. You will work closely with manufacturers, clients, and internal teams while contributing to a robust quality culture within a highly regulated environment.

You will become part of a CRO specialized in analytical services for the pharmaceutical and biotechnology industries, where you will gain exposure to a wide range of pharmaceutical products, quality systems,



and regulatory requirements while supporting activities critical to product release and patient safety.

The challenges you will take on:

- Review batch records, packaging records, and related documentation prior to product release.
- Support batch certification and release activities for commercial and clinical products.
- Participate in investigations of deviations, OOS, OOT results, complaints, CAPAs, and Change Controls, ensuring GMP compliance.
- Review and approve quality documentation, including CoAs, SOPs, Site Master Files, and product specifications.
- Review Quality and Technical Agreements and support audits and regulatory inspections.
- Contribute to the continuous improvement of the Quality Management System (QMS).

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📌 Qa scientist for batch release (Cataluña)
🏢 Kymos Group
📍 Cataluña