Sr. Quality Specialist, Compliance & Supplier Quality

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day.

We're Par Health, the essential pharmaceutical company, making quality generic medicines people can count on-leading with excellence and committed to those we serve. With 4,000 team members worldwide, our reputation is built on reliability, compliance, and service-because patients depend on it. With approximately 80 product families, our broad product portfolio spans multiple therapeutic areas, dosage forms and delivery technologies, including oral solids, liquids, sprays, patches, and more designed to meet the needs of patients and healthcare providers.

From everyday medicines to specialized care, we're here to advance better health.

At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day.

The Senior Quality Specialist, Compliance & Supplier Quality is responsible for independently owning, planning and conducting activities that ensure the supplier management program for PAR Health meets cGMPs and regulations as well as internal quality procedures/governance. The Supplier Quality Specialist is accountable for ensuring that materials, components, and services provided by suppliers meet company quality standards and regulatory requirements. This role works cross functionally with procurement, quality, engineering, and suppliers to drive continuous improvement, resolve quality issues, and maintain a robust supplier quality management system.

. Owns material non-conformance program and end-to-end supplier initiated changes (SIC) to completion.

Provides SME consultative support for all regulatory audits, internal and external inspections and other audits. Leads cGMP projects for continuous improvement to ensure compliance with regulations and current industry standards. Implements a self-inspection program and evaluates metrics to determine trends and opportunities for continuous improvements and liaises with QS&T and other departments.

Maintains and communicatest monthly metrics to site leadership.

• Independently evaluates supplier quality documentation to determine acceptability and compliance with applicable requirements.
• Independently manages the resolution of supplier quality issues and identifies opportunities for improvement.
• Drives the timely receipt and approval of acceptable quality documentation from suppliers.
• Manages supplier documentation requirements and assesses supplier TUP questionnaires.
• Ensures adherence to applicable SOPs, policies, regulations, and quality standards.
• Ensures procedures accurately reflect current practices, regulatory requirements, and industry guidance.
• Serves as a subject matter expert (SME) and provides consultative support for regulatory inspections, internal and external inspections, and other audits.
• Supports the development, implementation, and maintenance of the facility FDA Readiness Plan.
• Partners with Supply Chain and Site Quality to ensure manufacturing needs are met while maintaining quality and compliance requirements.
• Partners with Technical Operations and Site Quality to execute the TUP program.
• Owns and leads the end-to-end Supplier Performance and Supplier-Initiated Change programs.
• Evaluates, qualifies, and monitors suppliers to ensure compliance with company requirements and applicable industry quality standards.
• Owns and leads the end-to-end Nonconformance Material Review (NCMR), Corrective and Preventive Action (CAPA), and Supplier Corrective Action Request (SCAR) programs.
• Implements and manages a self-inspection program; evaluates metrics to identify trends, risks, and opportunities for continuous improvement and collaborates with QS&T and other departments as appropriate.
• Leads cGMP projects and continuous improvement initiatives to ensure compliance with applicable regulations and current industry standards.
• Actively evaluates quality and supplier performance metrics to identify trends, risks, and opportunities for continuous improvement.
• Drives continuous improvement initiatives with suppliers and across facility quality programs.
• Travels to supplier locations, as necessary, to ex