Teams at BISCO Inc.

Manage and maintain the Quality Management System for ISO 13485 and medical device regulatory compliance. Oversee QA/QC activities, CAPA, complaints, internal audits, receiving inspection, and QC lab operations. Lead and coach direct and indirect reports, support eQMS use, perform quality data and trend analysis, drive corrective actions, support validation and audit readiness, and partner cross-functionally to resolve quality issues and support continuous improvement.

Lead Production Engineer responsible for managing and validating production equipment, troubleshooting, implementing corrective actions, driving automation and robotics solutions, supporting capacity planning, ensuring GMP and ISO 13485 compliance, leading continuous improvement projects, mentoring technicians, and acting as technical lead and backup support for packaging supervision.

Design and create labels, packaging, marketing collateral, and ads; manage proofs and vendor submissions; maintain labeling review/approval records; provide creative support for company programs and events; ensure regulatory compliance and quality assurance; collaborate across teams and manage multiple projects to deadlines.