This position will have the option to work a hybrid schedule, with two days from home after three months of employment, with the remainder working in our office out of Schaumburg, IL.

BISCO is seeking a Senior Post-Market Surveillance Specialist who will own and evolve our Post-Market Surveillance (PMS) processes across the organization. This role goes beyond document preparation. It requires working with cross-functional teams and driving clarity across varying inputs and perspectives.
The ideal candidate is comfortable making decisions in evolving situations, can influence without direct authority, and brings clear recommendations rather than open-ended analysis. This role requires both independent ownership and the ability to engage leadership as a thought partner, bringing forward direction while incorporating feedback.
This position will plan, execute, and continuously improve Post-Market Surveillance processes and support Clinical Evaluation Reports throughout the product life cycle.

Salary range: $81K-$95K, commensurate with experience
Benefits: Medical, dental, and vision insurance, HRA and FSA, short and long-term disability, life insurance, pet insurance, PTO, 401(k) profit-sharing with match, potential year-end bonuses.

RESPONSIBILITIES of the Senior Post-Market Surveillance Specialist:
The job responsibilities of this position may include, but are not limited to:
- Own, plan, author, and maintain Post-Market Surveillance documentation, including Post-Market Surveillance (PMSP/PMSR), Periodic Safety Update (PSUR), Post-Market Clinical Follow-Up (PMCFP/PMCF)
- Drive clarity and consistency in PMS inputs across cross-functional teams
- Identify opportunities to improve inputs and partner with leadership to enhance data quality and reporting
- Provide clear recommendations and decision direction on PMS-related topics rather than open-ended analysis
- Review and provide guidance on Clinical Evaluation Reports (CERs)
- Author the Summary of Safety and Clinical Performance (SSCPs)
- Assist in the review of General Safety and Performance Requirements and Essential Principles in design and development
- Interpret clinical, scientific, and risk data to support regulatory submissions and product decisions
- Interprets results in preparation for product applications by evaluating clinical, scientific, risk data, and literature while staying abreast of current clinical practice
- Monitor post-market surveillance and clinical regulatory requirements and trends as part of the Regulatory Intelligence process
- Participate in the development of regulatory responses for Notified Body submission questions
- Contribute to the risk management process, ensuring integration of clinical and PMS data
- Support development and implementation of global clinical regulatory strategies for new and legacy devices

Role Expectations:
- Bring forward clear recommendations rather than open-ended analysis
- Lead discussions on complex topics and help drive toward decisions
- Engage leadership as a thought partner while maintaining ownership of outcomes
- Take initiative to improve how information is gathered and used across teams
- Influence cross-functional stakeholders to drive alignment and consistency
- Use sound judgment to determine when to act independently and when to align
- Simplify complex situations into clear, actionable direction

Requirements:

- Bachelor’s degree required. Advanced degree preferred. Degree in science, medicine, dentistry, or similar discipline highly preferred.
- Minimum of 5 years professional experience including medical/technical writing experience.
- Experience authoring, EU MDR compliant, medical device Post-Market Surveillance reports preferred.
- Detailed knowledge of relevant MDCG guidance preferred.
- Familiarity with relevant international regulatory requirements and guidance documents for medical devices, including MEDDEV 2.7/1 revision 4
- Familiarity applying research methodology and information management.
- Experience in the medical device industry, within a Quality Management System preferred
- Proficient in MS Office applications (Word and Excel) and email systems.
- Strong organizational and follow-up skills, as well as attention to detail.
- Strong English writing and communication skills

How to Apply:

Please submit your resume for consideration.
A cover letter is optional, but we welcome one to provide additional context on your experience or approach to your work.

Why BISCO, INC.?

Bisco, Inc. stands out because of our culture and core values:
o Respectful – Professional. Humble. Considerate.
​​​​​​​o Positive – Friendly. Inclusive. Curious.
​​​​​​​ ​​​​​​​o 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 medical and dental products to dental customers around the world. Our primary focus is adhesive and composite technology. Located northwest of Chicago in Schaumburg, our advanced research facility includes on-site ISO 13485 certified manufacturing. Our privately-owned organization provides the opportunity for a close-knit environment that encourages inter-departmental collaboration. For more about us, please visit our website at www.bisco.com.

Hours: 8:00 a.m. to 4:30 p.m., Monday-Friday
EOE
No agencies please.