Public summary
An internship opportunity supporting compliance and quality management tasks within a biopharmaceutical company focused on personalized cell and gene therapies. The role involves assisting with quality documentation maintenance, training record management, compliance tracking, and administrative support to ensure audit-ready records and adherence to regulatory requirements. The position is based in Bergisch Gladbach with options for some remote work and offers experience in a regulated healthcare environment.
Location and work setup
- Location
- Bergisch Gladbach
- Remote status
- Hybrid
- German requirement signal
- No German Required Detected
- Detected job language
- English
Responsibilities
Support maintenance, organization, and archiving of quality and compliance documentation; assist with training documentation tracking and filing; perform administrative document reviews for completeness and accuracy; support tracking and follow-up of Corrective and Preventive Actions (CAPAs); maintain quality and compliance activity logs; prepare meeting minutes and document action items; coordinate and follow up on administrative tasks; contribute to inspection- and audit-ready documentation; support sponsor oversight documentation; assist with general quality management administrative tasks.
Qualifications
Currently enrolled in a Bachelor's or Master's program in Life Sciences, Pharmacy, Biotechnology, Biology, Biomedical Sciences, Healthcare Management, or related field; strong interest in clinical research, quality management, and regulatory compliance; good organizational skills and attention to detail; proficient in Microsoft Office; good English communication skills. Preferred: initial knowledge of Good Clinical Practice (GCP), clinical research or quality management systems; experience with document management or electronic filing systems; structured and detail-oriented, reliable, proactive, team player with willingness to learn in a regulated healthcare environment.