Senior Quality Incoming/Process Supervisor

About the role

We are looking for a Senior Quality Incoming/Process Supervisor to lead our Quality Control teams across incoming, in‑process, and finished‑product inspections. You will ensure product compliance, support manufacturing goals, and maintain regulatory standards in a fast‑paced medical device environment.

Key responsibilities

• Lead and supervise QC teams performing inspections, document review, and validation testing.
• Manage daily quality operations across shifts to meet release timelines and regulatory compliance.
• Review and approve quality records, inspection results, and batch documentation.
• Coordinate product holds, disposition activities, non‑conformance investigations, and corrective‑action implementation.
• Monitor quality metrics and trends to drive process improvements and data‑based decisions.
• Develop, train, and evaluate QC personnel to ensure consistent execution of quality procedures.
• Partner with Engineering, Manufacturing, and other functions to communicate quality requirements and support product/process improvements.
• Support internal and external audits and maintain compliance with applicable quality system and regulatory requirements.

Required profile

• Bachelor’s degree in Engineering or a related technical field.
• Minimum 5 years of experience in Quality Engineering, Quality Control, or Quality Assurance within a regulated manufacturing environment.
• At least 2 years of experience leading or supervising quality personnel.
• Advanced proficiency in English (written and verbal).
• Advanced proficiency in Spanish (written and verbal).

Required skills

• Strong knowledge of Quality Management System regulations, ISO 13485, and MDSAP.
• Experience with corrective and preventive actions, non‑conformance investigations, and root‑cause analysis.
• Experience supporting internal and external quality audits.