Bryan Dillon Email & Phone Number

Brussels, BE

Marlborough, MA, US

• Led team of engineers for Endoscopy and Urology franchises in developing/maintaining a robust external (CM & OEM) supplier base, including M&A integration.
• Drove strategic business initiatives to increase performance/capabilities of external suppliers, through process improvement or risk reduction projects.
• Managed workload prioritization, performance evaluations, hiring, & employee coaching/development to build strength across operations and encourage learning, development, and leadership.
• Developed and reported monthly KPI/Metric Dashboard to leadership.

Marlborough, MA, US

• Managed cross functional projects with Contract Manufacturers or key suppliers to support the day to day operations success within the Sourced Finished Medical Device group.
• Projects included process improvements, cost reduction initiatives, and new equipment installation/validation as well as working with suppliers on manufacturing issues.

Lawrence, Massachusetts, US

• Led development of dialysis fluids at external contract manufacturers.
• Project Management responsibilities included developing and maintaining timelines, deliverables, and projects costs.
• Engineering responsibilities included developing system specifications, validation plans, protocols, and reports. Performed required device and pharmaceutical tests to support regulatory filings, such as.

Acton, Massachusetts, US

• Managed a team of engineers and designers supporting new and sustaining engineering projects.
• Responsible for scheduling, workload balancing, task prioritization, hiring, and performance reviews.
• R&D resource for documentation approval (ECOs, deviations, NCRs) for overseas Contract Manufacturer.
• Reported status updates and proposed new projects to Project Review Committee.
• R&D support for new sterilization validations, product aging studies, and biocompatibility.

Acton, Massachusetts, US

• Launched next generation disposable device with overseas Contract Manufacturer by taking concepts from CAD design (Pro-Engineer and Solidworks) through manufacturing including component sourcing, qualification (IQ, OQ.
• Managed biocompatibility, extractables, leachables testing to ISO 10993.
• R&D resource to support Risk Management update from 2007 to 14971:2012.
• Developed and implemented design verification plans.

Aliso Viejo, CA, US

• Responsible for the introduction of two innovative electromechanical medical devices, including one as a Class III Device (Drug / Device Combination).
• Developed assembly processes (Travelers/WIs) to document assembly/testing of a finished device.
• Designed and qualified fixtures to aid in inspecting components or assembling devices.

Acton, Massachusetts, US

• Developed and scaled up medical device components to bring Class II drug delivery device to a mass market.
• Delivered project plans based on internal requirements.
• Performed DFM, associated testing or tolerance stack-ups, and processed ECO’s for changes.

Acton, MA, US

• Responsible for development and commercialization of multi-million dollar interior automotive trim programs.
• Completed internal and customer required testing and documentation for PPAP submissions.
• Supported external customers by attending on-site trials of new materials or critical aspects of a program launch.
• Developed new constructions/coatings for innovative welding/low-pressure molding of door panels.
• Evaluated sample material for new development programs and cost reductions on lab and pilot lines.

Mentor, Ohio, US

Accountable for major and minor projects in an ISO 14000 / Six Sigma environment while also receiving hand on training in injection molding and extrusion processing, execution of design of experiments (DOE), Quality Assurance testing, and mold maintenance / repair.

Master Of Science (Ms), Plastics Engineering

Master Of Business Administration (Mba), Entrepreneurship/Entrepreneurial Studies

Bachelor Of Science (Bs), Plastics Engineering