Job Description
BISCO, INC. is a company dedicated to quality and innovation in dental medical devices. They are seeking a Regulatory Affairs Associate to gain hands-on experience in product registration and compliance while supporting a collaborative Regulatory Affairs team. Responsibilities Prepare and organize documentation for domestic and international regulatory submissions to support product approvals Maintain regulatory files and databases, and update information in internal systems to ensure accuracy and compliance Review documentation for regulatory compliance, including labeling and standard operating procedures Research regulatory requirements and assist with planning discussions to support submission strategies Collaborate with internal teams and external partners to facilitate smooth registration processes Skills Bachelor's degree in a science field (e.g., Chemistry, Microbiology, Biology, Biochemistry or Engineering) 1+ years of regulatory affairs experience preferred Comfortable using bolthires Office applications (Word and Excel) and common digital tools such as email and internet-based platforms Strong English writing and communication skills Exceptional attention to detail and accuracy in all tasks Organized and able to manage multiple priorities with confidence Curious and eager to learn, with a proactive approach to problem-solving Collaborative team player who adapts easily to changing priorities Benefits Medical Dental And vision insurance HRA and FSA Short and long-term disability Life insurance PTO 401(k) profit-sharing with match And potential year-end bonuses Company Overview For over 30 years BISCO has been a global leader in aesthetic dentistry and we continue to develop innovative products for contemporary dentistry.
It was founded in 1981, and is headquartered in Schaumburg, Illinois, USA, with a workforce of 51-200 employees. Its website is