BISCO Dental Products
Regulatory Affairs Associate
BISCO, INC. Schaumburg, IL
Enjoy the flexibility of a hybrid schedule after your first three months, with two days from home and the remainder on site in Schaumburg, IL. This position is primarily onsite.
Ready to launch your career in Regulatory Affairs? Join our collaborative team dedicated to quality and innovation in dental medical devices. You’ll gain hands‑on experience in product registration and compliance while working in a supportive environment that values learning, growth, and making an impact in a global industry.
Salary range: $55K to $64K, commensurate with experience.
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.
Responsibilities of the Regulatory Affairs Associate
Prepare and organize documentation for domestic and international regulatory submissions to support product approvals.
Maintain regulatory files and databases, 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.
QUALIFICATIONS Required
Bachelor’s degree in a science field (e.g., Chemistry, Microbiology, Biology, Biochemistry or Engineering)
1+ years of regulatory affairs experience preferred
Comfortable using Microsoft 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
WHY BISCO, INC.?
Respectful – Professional. Humble. Considerate.
Positive – Friendly. Inclusive. Curious.
Team Player – Helpful. Cooperative. Flexible.
Agility of a small company, but the stability of a big company
Industry‑leading dental restorative products
Broad exposure to activities across the company
Family‑oriented environment with positive team players
Approachable, respectful, and down‑to‑earth people
Long‑tenured employees to whom the leadership is committed
Employees feel valued and are proud to be a part of the company
Monthly whole‑company fun events!
Since 1981, BISCO has provided innovative dental restorative products to dental customers around the world. Our primary focus is on adhesive and composite technology. Located northwest of Chicago in Schaumburg, our ISO 13485 certified facility includes on‑site manufacturing and research. Our privately‑owned organization provides the opportunity for a close‑knit environment that encourages inter‑departmental collaboration. For more information about us, please visit our website at www.bisco.com.
This is an excellent opportunity to make an impact and to grow professionally, while contributing to the company’s success!
How to Apply Please submit your resume for consideration. While a cover letter is optional, we’d love to hear why you’re excited about starting your career in Regulatory Affairs and what makes you a great fit for this role.
Hours: 8 a.m. to 4:30 p.m., Mon‑Fri
EOE
No agencies please
#J-18808-Ljbffr
Enjoy the flexibility of a hybrid schedule after your first three months, with two days from home and the remainder on site in Schaumburg, IL. This position is primarily onsite.
Ready to launch your career in Regulatory Affairs? Join our collaborative team dedicated to quality and innovation in dental medical devices. You’ll gain hands‑on experience in product registration and compliance while working in a supportive environment that values learning, growth, and making an impact in a global industry.
Salary range: $55K to $64K, commensurate with experience.
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.
Responsibilities of the Regulatory Affairs Associate
Prepare and organize documentation for domestic and international regulatory submissions to support product approvals.
Maintain regulatory files and databases, 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.
QUALIFICATIONS Required
Bachelor’s degree in a science field (e.g., Chemistry, Microbiology, Biology, Biochemistry or Engineering)
1+ years of regulatory affairs experience preferred
Comfortable using Microsoft 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
WHY BISCO, INC.?
Respectful – Professional. Humble. Considerate.
Positive – Friendly. Inclusive. Curious.
Team Player – Helpful. Cooperative. Flexible.
Agility of a small company, but the stability of a big company
Industry‑leading dental restorative products
Broad exposure to activities across the company
Family‑oriented environment with positive team players
Approachable, respectful, and down‑to‑earth people
Long‑tenured employees to whom the leadership is committed
Employees feel valued and are proud to be a part of the company
Monthly whole‑company fun events!
Since 1981, BISCO has provided innovative dental restorative products to dental customers around the world. Our primary focus is on adhesive and composite technology. Located northwest of Chicago in Schaumburg, our ISO 13485 certified facility includes on‑site manufacturing and research. Our privately‑owned organization provides the opportunity for a close‑knit environment that encourages inter‑departmental collaboration. For more information about us, please visit our website at www.bisco.com.
This is an excellent opportunity to make an impact and to grow professionally, while contributing to the company’s success!
How to Apply Please submit your resume for consideration. While a cover letter is optional, we’d love to hear why you’re excited about starting your career in Regulatory Affairs and what makes you a great fit for this role.
Hours: 8 a.m. to 4:30 p.m., Mon‑Fri
EOE
No agencies please
#J-18808-Ljbffr