THE PROJECT:
Join the Quality area of the Advanced Therapies Platform (PTA), participating in quality control activities for advanced therapy products, in classified facilities and in compliance with GMP regulations.
RESPONSIBILITIES:
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Coordinate and carry out laboratory analytical activities.
- Perform quality control techniques for advanced therapy products in the classified facilities of the PTA, in compliance with GMP regulations.
- Coordinate, plan and participate in analytical method validations.
- Provide technical support to laboratory staff in the execution of analytical techniques and the resolution of operational incidents.
- Carry out environmental microbiological control activities in the PTA facilities.
Attend general laboratory meetings and participate actively.
- Attend scheduled training sessions.
- Participate in the training processes of newly hired technical staff.
- Contribute to the continuous improvement of the activities carried out in the PTA.
- Respect the confidentiality of all information received and generated at Hospital Sant Joan de Déu.
- Participate in the development and maintenance of the PTA quality management system.
- Supervise the correct completion of GMP documentation associated with Quality Control activities.
- Actively participate in the investigation and follow-up of deviations, OOS, incidents and CAPA related to the Quality Control area.
- Collaborate in the organization and prioritization of the laboratory’s daily activities according to the operational needs of the PTA.
SCHEDULE AND CONTRACT:
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The position will be full-time.
- Working hours from 8:00 a.m. to 3:26 p.m., with the possibility of occasional adjustments according to service needs.
- Permanent contract.
THE PROFILE WE ARE LOOKING FOR:
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Hold a qualification as a Specialist Technician in Clinical Diagnostic Laboratory, FPII or Higher Vocational Training Cycle, Degree in Biology or similar.
- Training in biosafety, laboratory quality control and cell culture techniques.
- Proficiency in auxiliary laboratory instruments and basic IT skills.
- Systematic, methodical, organized and precise profile.
- Responsibility, discipline and rigor in the execution of tasks.
- Ability to work in a team and collaborate with different professionals.
- Autonomy and ability to make decisions within the scope of the role.
WE VALUE:
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Previous experience in a clinical laboratory or cell culture laboratory.
- Experience in GMP environments.
- Experience in quality control within a laboratory setting.
- Collaborative approach and orientation towards continuous improvement.
DOCUMENTATION TO SUBMIT:
To apply for this job offer and attach your Curriculum Vitae, click on the “Apply” button displayed on this same screen. The application submission period will be 20 calendar days from the publication date of this call.
We encourage you to focus your application on your experience and skills. It is not necessary to include a photograph, gender or age.
Esplugues de Llobregat, 27/05/2026
