Pharmacy Intern for Quality Assurance and Quality Control

We are a company of the Adragos Pharma Group and produce high-quality pharmaceuticals, cosmetics, and dietary supplements at our site in Leipzig using modern facilities. High quality standards and the ambition to continuously develop our work shape our daily actions. A corporate culture characterized by appreciation and respect for our employees, as well as long-standing and trusting customer relationships, form the basis for our shared success.

• A varied range of tasks
• Flat hierarchies, short decision-making paths
• 15 days of recreational leave (for 6 months) and attractive statutory remuneration
• Release from work for attending accompanying educational events
• Participation in summer and Christmas parties, company runs, and other events

As part of the internship, you will undertake various tasks in the areas of galenics, manufacturing, quality control, and quality assurance. You will learn about all GMP-relevant processes of a pharmaceutical company through the interface of quality assurance and actively contribute to current, exciting key topics. Furthermore, you will gain practical insights into the manufacturing, packaging, and testing of pharmaceuticals, dietary supplements, cosmetics, and medical devices.
Here you can leverage your university knowledge of analytical chemistry and instrumental analytics, such as HPLC, UV-VIS, and practically expand your skills. You will take responsibility for the development and validation of analytical methods for the area of cleaning validation. In quality control, you will independently perform raw material analytics according to the European Pharmacopoeia, finished product analytics, and stability tests, and document your work in accordance with GMP. All of this will be done independently and with excellent support from our experienced specialists.

Technical Requirements

• Completed pharmacy studies or completed Second State Examination
• Willingness to familiarize yourself with quality-relevant processes, pharmaceutical manufacturing, and regulatory requirements
• Proficient in common MS Office applications
• Very good German language skills and good English language skills, both written and spoken

• High quality awareness and structured way of working
• Diligence, reliability, and adherence to deadlines
• Analytical thinking and enjoyment of documentation and evaluation tasks
• Strong communication skills and teamwork ability
• Independent, responsible work ethic

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