What are the responsibilities and job description for the Director of Quality and Compliance position at CoValence Laboratories?
CoValence Laboratories is seeking an experienced and dynamic QC Director to oversee the regulatory compliance and quality control functions within the company. This key leadership role will ensure compliance with company standards, FDA, cGMP, GDP, and other regulatory requirements. The QC Director will be responsible for identifying potential areas of compliance vulnerability and risk, developing remediation guidance, and ensuring that the quality of manufactured goods meets the highest standards. This position requires collaboration with multiple departments to ensure full compliance across all aspects of the company and will involve direct oversight and management of the quality control and compliance teams.
Key Responsibilities:
- Oversee regulatory compliance and quality control functions in accordance with company policies, FDA, cGMP, GDP, and other relevant requirements.
- Identify potential areas of compliance vulnerability and risk, and develop and implement appropriate remediation strategies.
- Collaborate with cross-functional teams (e.g., manufacturing, R&D, operations) to ensure compliance across all aspects of the organization.
- Ensure the quality of manufactured goods through the establishment and management of robust supplier quality, quality control, and process monitoring programs.
- Propose and manage corrective actions to maintain compliance with Quality, cGMPs, GDPs, and other company-directed areas of compliance.
- Provide leadership and guidance to the QC team, including managing personnel, developing training programs, and ensuring high performance across the department.
- Stay up to date with industry trends, regulatory changes, and best practices to ensure the company maintains a competitive edge in quality management.
Job Type: Full-time
Schedule:
- 8 hour shift
- Monday to Friday
Ability to Commute:
- Chandler, AZ 85224 (Required)
Work Location: In person