Lead GMP Process Specialist
vor 1 Monat
About the Role:
CSL Behring is seeking a highly skilled Lead GMP Process Specialist to join our team. In this role, you will be responsible for overseeing the quality processes and standards across the network in your area of responsibility.
Key Responsibilities:
- Develop and implement Globally Owned Processes Quality Management System
- Maintain Site Bern Ownership (Deviation Management System)
- Analyze quality trends in your area of responsibility
- Support quality relevant projects and initiatives
- Design and execute trainings/awareness related to GMP standards
- Provide training to your area of responsibility
- Liaise with Global Quality Systems and other Quality functions
Qualifications and Requirements:
- University degree or university of applied sciences degree in natural sciences (e.g. Biology, Chemistry or Pharmacy)
- At least 3+ years experience in Quality or manufacturing in a pharmaceutical GMP environment or equivalent
- Thorough knowledge of current Good Manufacturing Practices (cGMP) principles
- Familiarity with Authority Requirements
- Fluent in English
Salary and Benefits:
The estimated salary for this position is around $85,000 per year, depending on qualifications and location. We also offer a range of benefits, including health insurance, retirement plan, and opportunities for professional growth.
About CSL Behring:
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
Career Opportunities at CSL Behring:
We are committed to fostering an inclusive workplace culture that reflects the diversity of our patients and communities. If you are passionate about working in a dynamic and supportive environment, we encourage you to apply for this exciting opportunity.
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