Life Sciences Internship at Miltenyi Biomedicine, Germany | Apply Now For Compliance & Quality Role
The Miltenyi Biomedicine Internship offers aspiring professionals a chance to join the company as an Intern in Compliance & Quality Support. Located in Bergisch Gladbach, North Rhine-Westphalia, Germany, this Life Sciences Internship opportunity offers a chance to contribute to the advancement of personalized cell and gene therapies.
- Position: Intern – Compliance & Quality Support (m|f|d)
- Location: Bergisch Gladbach, North Rhine-Westphalia, Germany
About The Company
Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. The organization is pioneering groundbreaking therapies for serious life-threatening diseases and reshaping their accessibility for clinical professionals and patients worldwide, with the aim to improve and extend patients’ lives. Currently, Miltenyi Biomedicine is focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases.
Miltenyi Biomedicine Internship: Job Description
The Life Sciences Internship involves supporting the CTQC and ClinDevEU teams in administrative and documentation-related compliance activities. Under supervision, the role contributes to maintaining inspection- and audit-ready documentation, supporting training record management, tracking quality actions, and ensuring the accurate organization of quality-related records in accordance with internal procedures and applicable regulatory requirements.
Life Sciences Internship – Key Responsibilities
- Support the maintenance, organization, and archiving of quality and compliance documentation
- Assist with training documentation tracking and filing activities
- Perform administrative reviews and document pre-filing checks to ensure completeness and accuracy
- Support the tracking and follow-up of Corrective and Preventive Actions (CAPAs)
- Assist in maintaining trackers and logs related to quality and compliance activities
- Prepare meeting minutes and document action items from team meetings
- Support the coordination and follow-up of assigned administrative tasks
- Contribute to maintaining inspection- and audit-ready documentation
- Support sponsor oversight documentation activities as applicable
- Assist the team with general quality management and compliance-related administrative tasks
Eligibility Criteria Required For Life Sciences Internship
Required
- Currently enrolled in a Bachelor’s or Master’s degree program in Life Sciences, Biotechnology, Biology, Biomedical Sciences, or a related field
- Strong interest in clinical research, quality management, and regulatory compliance
- Good organizational skills and attention to detail
- Proficient in Microsoft Office applications (Word, Excel, PowerPoint, Outlook)
- Good written and verbal communication skills in English
Preferred
- Initial knowledge of GCP (Good Clinical Practice), clinical research processes, or quality management systems
- Experience with document management systems or electronic filing systems
Competencies
- Structured and detail-oriented working style, essential for a Life Sciences Internship
- Strong organizational and documentation skills
- Ability to handle confidential information professionally
- Reliable and proactive approach to assigned tasks
- Ability to work effectively in a team environment
- Willingness to learn and develop in a regulated healthcare environment
What Miltenyi Biomedicine Offers?
- A modern workplace in Bergisch Gladbach with opportunity for some mobile work. Exciting opportunities in the development of technologies with a secure future.
- Cross-border intercultural cooperation and short communication channels
- A collegial corporate culture and flexible working hours enable time management on your own terms
- Personalized employee development program: specialist and personal training courses provided by Miltenyi University
This Life Sciences Internship at Miltenyi Biomedicine presents a unique chance for candidates to gain valuable experience in compliance and quality support within a leading biopharmaceutical company. Interested individuals are encouraged to apply.
