14 May 2026

Team Lead, Receiving & Inspection

Insulet Corporation

Waalwijk

14 May 2026

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Insulet is seeking a hands-on Team Lead for Receiving & Inspection in its Quality Department in Waalwijk, Netherlands. The role manages return sample intake, ensures compliance with FDA/ISO standards, and leads a team in medical device handling.

On-siteFull-timeEntry LevelDevice History Records (DHRs)Nonconforming Material Reports (NCMRs)

Team Lead, Receiving & Inspection

Apply

On-siteFull-timeEntry LevelDevice History Records (DHRs)

Salary

Not specified

Work Location

Waalwijk, North Brabant, Netherlands, NL

Work Model

On-site

Employment Type

Full-time

Experience Level

Not Applicable

Core Qualifications

Technical (Must-have)

Device History Records (DHRs)Nonconforming Material Reports (NCMRs)Corrective and Preventive Actions (CAPAs)ISO 9001ISO 1348521 CFR Part 820

Soft Skills

leadershipmentoringtrainingcommunicationorganizationalattention to detailproblem solving

Key Responsibilities

•Lead the Post Market Receiving & Inspection team in managing return sample intake, handling, and documentation.
•Track and report daily team metrics to ensure performance targets are met.
•Maintain relationships with device return distributors and external partners.
•Coordinate and monitor global device returns through reverse logistics pathways.
•Provide mentorship and work leadership to team members, including training on processes and procedures.
•Ensure compliance with quality and safety standards across all receiving and inspection activities.
•Implement and maintain effective processes to support operational excellence.
•Develop and update protocols and standards to meet quality specifications; recommend procedural improvements.
•Review Device History Records (DHRs), Nonconforming Material Reports (NCMRs), Corrective and Preventive Actions (CAPAs), and deviations related to individual complaints.
•Manage, facilitate, and participate in continuous improvement projects.

Team LeadReceiving & InspectionQuality DepartmentMedical DevicesFDAISO 13485NetherlandsWaalwijkFull-timeOn-site

Key Responsibilities

•Lead the Post Market Receiving & Inspection team in managing return sample intake, handling, and documentation.

•Track and report daily team metrics to ensure performance targets are met.

•Maintain relationships with device return distributors and external partners.

•Coordinate and monitor global device returns through reverse logistics pathways.

•Provide mentorship and work leadership to team members, including training on processes and procedures.

•Ensure compliance with quality and safety standards across all receiving and inspection activities.

•Implement and maintain effective processes to support operational excellence.

•Develop and update protocols and standards to meet quality specifications; recommend procedural improvements.

•Review Device History Records (DHRs), Nonconforming Material Reports (NCMRs), Corrective and Preventive Actions (CAPAs), and deviations related to individual complaints.

•Manage, facilitate, and participate in continuous improvement projects.