Senior Specialist - Camp Springs, MD, United States - Titan Industries
Description
CureVac Manufacturing GmbH, a 100% subsidiary of CureVac SE, is a biopharmaceutical production company that manufactures novel medicines based on the messenger RNA (mRNA) molecule.
Our focus is on prophylactic vaccines, innovative cancer immunotherapies, and protein-based therapies.Currently, all of our RNA people are dedicated to achieving our big goal:
to bring several best-in-class mRNA medicines to the market.
To support our team at our Camp Springs, MD location, we are currently seeking a:
Senior Specialist (m/f/d) Production Support
Your responsibilities:
- Coordination of GMPrelevant support activities for the documentation of clinical trial materials in various stages of development, in close collaboration with Quality Assurance
- Coordination, tracking, and execution of crossfunctional activities throughout the document flow, from batch production registration to document review
- Creation of SOPs and other documents
- Implementation of temporary QA requirements within the team
- Development and implementation of continuous improvement projects and process optimizations in the documentation area
- Establishment of KPIs and processes for performance management/review within the team
- Support in team scheduling and acting as a subject matter expert for team leadership
- Organization of onboarding for new team members
Your qualifications:
- Completed degree in natural or engineering sciences, or a comparable qualification
- Professional experience in a GMPregulated environment, preferably in (bio)pharmaceutical manufacturing
- Indepth knowledge of
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