Staff Scientist, SEM-EDS (Hybrid - Acton, MA)

This Staff Scientist position will be integral in determining the design of disposable, class II/III medical devices and will be required to ensure our products are in compliance with ISO and USP standards.  The Staff Scientist will need to actively develop/execute internal testing protocols using SEM-EDS, FTIR, GCMS and LCMS etc.  This position will work closely with multiple R&D teams, Operations and QA/RA team to ensure products are adequately tested, results are documented and communicated in accordance to company procedures and 21 CFR Part 820. 

The Position will report to the Senior Principal Scientist of Chemistry/biocompatibility group in the Medical Devices Hardware Engineering team at Insulet’s Headquarters in Acton, MA.

Responsibilities:

• Conducts work using a safety-focused approach as well as a foundation grounded in ethics and data to inform outcomes and next steps

• Conduct internal testing using SEM-EDS and FTIR or other analytical instrumentation including GCMS and LCMS.

• Develop and validate test methods for internal test capabilities

• Coordinate contract lab activities regarding material characterization if needed.

• Collaborate with cross-functional teams to integrate research findings into product design and development

• Author product, material, and process qualification test protocols and reports

• Directly interface with supplier and operations engineering to ensure product remains compliant across multiple suppliers/materials/manufacturing sites

Education and Experience:

• Ph.D. degree (preferred field of study: Chemistry, Material Scientist or Biology) with at least 3 years of experience in Product Research & Development or Quality in Pharmaceutical and/or Medical Device industry; or Master's degree with at least 5 years of related experience; or Bachelor's degree with at least 8 years of related experience

• Extensive experience using/maintaining SEM-EDS and FTIR instruments

• Extensive knowledge of various material characterization methodologies

• Experience using LCMS or GCMS is a plus.

Preferred Skills and Competencies:

• Strong written, verbal, analytical, and interpersonal skills

• Highly ethical, responsible, and independent; demonstrates acceptance of responsibility and shows pride in work performed

• Experience and capability working independently and collaboratively under a Quality Management System (QMS), as part of a cross-functional team that includes development/verification/validation/procurement/manufacturing/regulatory and quality experts

• PC skills, word processing, spreadsheet, database, PowerPoint

• Ability to organize and judge priorities

• Ability to generate and maintain accurate records

Physical / Travel Requirements:

• Ability to pick up / move lab equipment or tools under 20 pounds

Additional Information:

• NOTE: This position is eligible for hybrid working arrangements (requires on-site work from an Insulet office). #LI-Hybrid

• Travel is estimated at 5% but will flex depending on business need

Additional Information:

Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $121,725.00 - $182,587.50 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including: • Medical, dental, and vision insurance • 401(k) with company match • Paid time off (PTO) • And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education.