We are looking for a motivated and detail-oriented Quality Assurance Intern to join our Batch Release team, with a specific focus on the preparation and coordination of Product Quality Reviews (PQRs) in compliance with EU GMP Annex 21 and internal quality procedures.
This internship offers hands-on experience in pharmaceutical quality systems, documentation management, and batch release processes within a highly regulated environment.
Key Responsibilities
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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 Good Manufacturing Practices (GMP) and company quality standards in all assigned activities.
What We Offer
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Internship in a dynamic QA environment.
- Exposure to real-life GMP processes and regulatory compliance activities.
- Mentorship and training from experienced QA professionals.
- Opportunity to gain insight into pharmaceutical batch release and product lifecycle management.
Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic
