Director, Quality Assurance

Avet Pharmaceutical; East Brunswick Township (NJ); Sur place; USD 170 000 - 200 000; Plein temps

Avantages offerts par ce poste

401(k) matching

Medical, Dental, Vision

Employee Assistance Program

Employee discount

FSAs

Résumé du poste

Avet Pharmaceutical seeks a Director of Quality Assurance to lead and optimize the cGMP program, audits, and regulatory readiness at the East Brunswick site.

The role directs QA systems, CAPA, batch disposition, deviations, investigations, and supplier qualification while partnering with Manufacturing, R&D, Engineering, Regulatory Affairs and other functions to ensure compliant products and processes.

Qualifications

• Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmacy, or related field.
• 10+ years in QA leadership within a cGMP environment, incl. OSd oversight.
• Deep knowledge of cGMP, cGLP, FDA/DEA regs and international requirements.

Responsabilités

• Provide strategic leadership of QA to ensure cGMP compliance and regulatory readiness.
• Coordinate audits, inspections, and responses with FDA/DEA and customers.
• Oversee supplier qualification, validation oversight, CAPA, investigations, and change control.
• Approve batch disposition based on quality standards; manage deviations.
• Lead internal self-inspection program and MRB governance; develop QA policies.

Connaissances

cGMP knowledge

Regulatory inspections

QMS leadership

CAPA management

Audit management

Cross-functional leadership

Risk assessment

Analytical skills

eQMS proficiency

Regulatory compliance

Formation

Bachelor's degree in science/related field

Outils

eQMS

Microsoft Office

Description du poste

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Director, Quality Assurance

Full Time Management E Brunswick, NJ, US

Salary Range: $170,000.00 To $200,000.00 Annually

Job Summary:

This position is responsible for providing strategic and operational leadership for the Quality Assurance function to ensure compliance with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements, including FDA, DEA, and other global regulatory agencies. The Director leads quality systems, regulatory inspection readiness, internal and external audit programs, supplier qualification, validation oversight, batch disposition, investigations, and continuous quality improvement initiatives. This role partners cross-functionally with Manufacturing, Research & Development, Engineering, Technical Services, Regulatory Affairs, and other business functions to develop and maintain compliant quality systems, drive corrective and preventive actions (CAPA), and ensure products, processes, facilities, and vendors consistently meet regulatory and company quality standards.

Reporting Relationships

• This is a supervisory leadership role responsible for overseeing 3 direct reports and 18 indirect reports.

Essential Functions:

• Provide strategic leadership and oversight of the Quality Assurance department to ensure compliance with cGMP regulations, FDA, DEA, and other applicable regulatory requirements.
• Direct and maintain the organization's quality systems to ensure continuous inspection readiness and regulatory compliance across manufacturing operations.
• Serve as the primary site coordinator for regulatory inspections, including FDA, DEA, customer, and third-party audits, ensuring successful inspection outcomes and timely resolution of observations.
• Lead quality oversight of manufacturing operations, contract manufacturers, contract packagers, contract testing laboratories, and suppliers to ensure compliance with established quality standards.
• Develop, implement, and maintain quality compliance strategies, policies, procedures, and systems aligned with business objectives and evolving regulatory requirements.
• Lead and oversee Corrective and Preventive Action (CAPA) activities, ensuring investigations are completed effectively and corrective actions are implemented and sustained.
• Review and approve validation protocols, validation reports, quality system documentation, investigations, deviations, change controls, and other Quality Management System (QMS) records.
• Exercise independent authority for batch disposition decisions, including approval or rejection of manufactured products based on compliance with established quality standards.
• Ensure deviations, nonconformances, and manufacturing investigations are thoroughly evaluated, documented, and resolved in accordance with regulatory expectations.
• Develop, implement, and manage the internal self-inspection program to assess compliance, identify risks, and drive continuous improvement initiatives.
• Oversee vendor qualification and auditing programs, including audits of raw material suppliers, packaging vendors, contract manufacturers, and contract laboratories.
• Partner with cross-functional departments including Research & Development, Manufacturing, Engineering, Technical Services, and Regulatory Affairs to establish compliant processes supporting product development and commercial manufacturing.
• Interface with regulatory agencies and external stakeholders regarding quality-related matters and represent the organization during inspections and compliance activities.
• Facilitate implementation of new quality systems, technologies, and process improvements that enhance compliance and operational efficiency.
• Chair or actively participate in Site Management Review Board (MRB) meetings and provide quality leadership for organizational decision-making.
• Provide leadership, coaching, performance management, and professional development for Quality Assurance personnel while fostering a culture of quality and regulatory compliance.
• Evaluate training needs and ensure personnel maintain required competencies related to cGMP regulations and quality systems.

Specialized Skills and Knowledge:

• Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• Minimum of ten (10) years of progressive Quality Assurance leadership experience within a cGMP-regulated generic pharmaceutical manufacturing environment, including oversight of Oral Solid Dosage (OSD) manufacturing, quality systems, validation, regulatory inspections, and management of Quality Assurance personnel.
• Extensive knowledge of current Good Manufacturing Practices (cGMP), current Good Laboratory Practices (cGLP), FDA regulations, DEA regulations, and applicable domestic and international pharmaceutical regulatory requirements.
• Comprehensive understanding of pharmaceutical manufacturing, quality assurance, quality control, validation, investigations, CAPA, change control, supplier qualification, and audit management.
• Demonstrated experience leading regulatory inspections and managing responses to regulatory observations.
• Strong knowledge of Quality Management Systems (QMS) and risk-based quality management principles.
• Experience interpreting and implementing regulatory guidance, industry standards, and quality compliance requirements.
• Excellent analytical, problem-solving, leadership, organizational, and communication skills.
• Proficiency with electronic Quality Management Systems (eQMS), Microsoft Office Suite, and applicable quality documentation systems.
• Regulatory Compliance & Quality Systems Leadership
• Strategic Leadership & Cross-Functional Collaboration
• Critical Decision-Making, Risk Assessment & Problem Solving

Physical Demands/Factors:

Work is performed in both office and pharmaceutical manufacturing environments. While performing the duties of this position, the employee is regularly required to sit, stand, walk, communicate, and use hands to operate office equipment.

The employee may occasionally be required to reach, bend, stoop, or lift up to 25 pounds. Periodic travel within manufacturing areas and to vendor or contract manufacturing sites may be required. Specific vision abilities include close vision, distance vision, color vision, and the ability to review detailed documentation.

Based on the highly regulated workplace at Avet, employees will be required to meet minimum English proficiency requirements.

All applicants must be legally authorized to work in the U.S. for any employer. We are unable to sponsor any applicants for a work visa or take over sponsorship of a work visa for any applicants, at this time.

Avet is proud to be an Equal Opportunity Employer.

This job description is not all-inclusive. It acts as a guideline and is subject to change over time. Additional duties may be assigned based on business needs.

Compensation and Benefits:

Compensation:

This is an exempt salaried position; the pay range is $170,000 to $200,000 per year.

In addition, this position is eligible for an annual bonus which aligns to both individual and company performance.

• 401 (k) matching - vested immediately
• Medical, Dental and Vision
• Employee Assistance Program
• Employee discount through Life Mart
• Flexible Spending Account and Dependent Care Account