QA Batch Release Trainee — PQRs & GMP Compliance

Kymos Group; Cerdanyola del Vallés; Presencial; EUR 8928 - 13.392; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Mentorship and training

GMP exposure

Regulatory compliance training

Descripción de la vacante

KYMOS GROUP in Spain is seeking a motivated Quality Assurance Intern to join our Batch Release team, with a focus on preparing Product Quality Reviews (PQRs) in compliance with EU GMP Annex 21. This internship offers hands-on experience in pharmaceutical quality systems, documentation management, and collaboration with QA professionals in a highly regulated environment.

You will benefit from mentorship and training, exposure to GMP processes, and opportunities to contribute to data integrity

Formación

• Degree or Masters in Pharmacy, Biotechnology, Chemistry, or related field.
• Good command of English (written and spoken).
• Basic understanding of EU GMP Annex 21 and PQR requirements is a plus.
• Strong attention to detail and analytical mindset.
• Familiarity with Excel and Word; experience with quality data systems is a plus.

Responsabilidades

• Support the preparation, review, and compilation of PQRs for commercial products according to EU GMP Annex 21 requirements.
• Assist in data collection, trending, and evaluation of product quality metrics, deviations, and CAPAs.
• Support QA Batch Release Scientists and QPs in the batch release documentation review process.
• Participate in continuous improvement initiatives related to PQR templates, procedures, and data integrity.
• Ensure compliance with GMP and company quality standards in all assigned activities.

Conocimientos

Attention to detail

Analytical mindset

Team player

English proficiency

Educación

Degree or Masters in Pharmacy/Biotech/Chemistry

Herramientas

Microsoft Excel

Microsoft Word

Quality data systems

Minitab

Descripción del empleo

KYMOS GROUP in Spain is seeking a motivated Quality Assurance Intern to join our Batch Release team, with a focus on preparing Product Quality Reviews (PQRs) in compliance with EU GMP Annex 21. This internship offers hands-on experience in pharmaceutical quality systems, documentation management, and collaboration with QA professionals in a highly regulated environment.

You will benefit from mentorship and training, exposure to GMP processes, and opportunities to contribute to data integrity