Headquartered in Brooklyn, New York, Cresilon, Inc. is a privately-held medical device company focused on hemostatic technologies that improve wound care and advance the standard of medical treatments. For more information, visit Cresilon.com. We are always looking for dynamic people to join our team as we dive into a range of challenges at the forefront of science and technology—to learn more about our openings please visit https://cresilon.workable.com/.
Open Positions
Senior Process Engineer/Process Engineer II - Manufacturing
5+ years of experience in a regulated manufacturing environment with at least 3+ years of process development, design, and process implementation required
Production Supervisor, 2nd Shift
Bachelor's degree, 3+ years of cGMP manufacturing experience, strong leadership skills, and experience in GMP cleanroom operations are required
Production Technician I, 2nd Shift Full-Time Monday-Friday
2+ years of manufacturing experience, high school diploma or equivalent, ability to read and execute written work instructions
Quality Assurance Technician
High school diploma, 1 year of experience in regulated industry, and ability to be Gowning Qualified
Research and Development Engineer I/II
4+ years of experience in an industrial environment, BS in Chemical Engineering or related field, mathematically inclined with strong analytical skills
Preclinical Principal Scientist, Research & Development
DVM, PhD, or MD; 6+ years of preclinical medical device research experience; 4+ years of people management experience
Manager/Principal Scientist Research & Development - Polymer Formulation
10+ years of research experience, Master’s degree, and 2+ years of management experience required
Research and Development Senior Medical Device Engineer
BS in Chemical Engineering, Polymer Engineering, Material Science, Biomedical Engineering, Mechanical Engineering, or related scientific discipline; A minimum of 5+ years of product development experience; A minimum of 4 years of hands-on experience in new product research and development in a cGMP-regulated industry
Temporary Executive Assistant
3-5 years of administrative experience, strong organizational skills, excellent communication