Cellipont Bioservices: Contract development and manufacturing organization for cell therapies.
Support GMP validation projects (IQ/OQ/PQ), execute protocols, generate and review validation documentation, apply cGMP and 21 CFR Part 11 principles, and work in controlled/lab environments.
Microsoft Word, Microsoft Excel, Microsoft Outlook
Cellipont Bioservices: Contract development and manufacturing organization for cell therapies.
5+ YOE3+ MgmtBachelor's in life sciences or chemical engineering, minimum 5 years GMP manufacturing experience, 3 years leadership in GMP, aseptic technique expertise, SOP/MBR/CAPA experience, Word and Excel proficiency.
Cellipont Bioservices: Contract development and manufacturing organization for cell therapies.
5+ YOE3+ MgmtBachelor's in Life Sciences or Chemical Engineering,5+ years GMP manufacturing experience,3+ years people management,aseptic processing,GMP/SOP/MBR experience,proficient in Microsoft Word and Excel,mechanical aptitude.
Cellipont Bioservices: Contract development and manufacturing organization for cell therapies.
5+ YOE2+ MgmtBachelor's in life science, 5+ years in CDMO/GMP environment, 2+ years project management, strong leadership, cross-functional team experience, excellent communication, analytical and problem-solving skills.
Business Development Manager - Small Molecule, Southern US
Houston or North Carolina or South Carolina or Florida or Texas or Georgia or Alabama or Tennessee or Mississippi or Arkansas or Louisiana or Oklahoma or New Mexico or Arizona
FieldFull Time
Eurofins ScientificEuronext Paris: ERF: Global provider of analytical testing and laboratory services.
2+ YOETerritory-based sales role requiring a bachelor’s degree in life sciences or business, ≥2 years biopharma sales/project experience in CDMO/CRO/CTO, ability to travel ≥40%, and U.S. work authorization.