Quality Supervisor​/Onsite​/Hyde Park, NY

Our client, a leader in global healthcare logistics, is looking to hire a Quality Supervisor
. This is a fully onsite position in New Hyde Park, NY!

* This role is a 6-month contract-to-hire W2 contract opportunity with benefits!*

As a Quality Supervisor, you will play a critical role in maintaining and enhancing the organization's Quality Management System (QMS),
ensuring regulatory compliance, and supporting quality initiatives across transportation and logistics operations
. You will serve as a key quality representative, partnering with operational teams, suppliers, auditors, regulators, and leadership to drive compliance, continuous improvement, risk management, and customer satisfaction.

• Manage and maintain the Quality Management System (QMS), ensuring quality objectives, policies, procedures, and performance metrics are effectively implemented
• Coordinate and support management review meetings in accordance with established SOPs and quality standards
• Administer supplier qualification and evaluation programs, including supplier approvals, audits, performance reviews, and corrective action initiatives
• Act as the primary point of contact for internal audits, external audits, inspections, and certification assessments
• Review and manage incidents, non-conformances, deviations, and customer complaints, supporting investigations, root cause analysis, CAPA development, and follow-up actions
• Support risk management and change control processes, ensuring regulatory and customer communication requirements are met

• 2-5 years of quality assurance, quality compliance, or quality management experience within a regulated industry
• Experience supporting or administering a Quality Management System (QMS)
• Knowledge of GDP, GxP, ISO standards, regulatory compliance requirements, and quality assurance principles
• Experience managing audits, inspections, deviations, CAPAs, investigations, and supplier quality activities
• Strong understanding of quality documentation, SOP management, and regulatory reporting requirements

• Associate's Degree or Bachelor's Degree or Diploma Pharmacy, Chemistry, Biochemistry, Pharmaceutical Sciences, Logistics, Engineering, Quality Management, or a related discipline
• Prior experience in healthcare, pharmaceutical, clinical, biotechnology, transportation, logistics, or highly regulated manufacturing environments
• Familiarity with Master Control, SharePoint, or other electronic quality management (QMS) systems
• Knowledge of Lean Six Sigma, Continuous Improvement, or Operational Excellence methodologies