Posted:16 hours ago|
Platform:
Work from Office
Full Time
1. Knowledge in quality principles driving drug development, such as GMP; understanding of general regulatory and quality expectations.
2. Good scientific background, communication skills including presentation and scientific/technical writing.
3. Minimum 5-7 years in a relevant position in a GMP environment.
4. Sound technical and regulatory knowledge. Working knowledge of pharmaceutical research and technical development.
5. Experienced in GMP environment, with familiarity with IT systems (e.g., eLN, GLIMS, SAP), and interfaces between different data tools.
Krystal Integrated Services
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