What are the responsibilities and job description for the Manufacturing Quality Manager position at NAZTEC Int. Group?
Job Summary:
We are seeking a dedicated Quality Director to uphold high standards and lead our Quality Management System. This role is responsible for overseeing the entire quality assurance and control processes in the manufacturing of dietary supplements, ensuring compliance with industry standards and regulatory requirements to maintain product safety, efficacy, and quality.
Key Responsibilities:
- Quality Management System (QMS):
- Develop and implement comprehensive QMS strategies ensuring compliance with cGMP, FDA, and other regulatory standards
- Monitor performance and enhance the QMS as needed
- Regulatory Compliance:
- Ensure strict compliance with all regulatory requirements for dietary supplements
- Facilitate audits and serve as the main contact point for regulatory bodies
- Leadership and Management:
- Lead and mentor the quality assurance and quality control teams, fostering a culture of continuous improvement
- Collaborate with cross-functional teams to drive quality-related initiatives
- Process Development and Improvement:
- Oversee the implementation and documentation of Standard Operating Procedures (SOPs)
- Identify areas for quality improvement and develop corrective action plans
- Supplier and Vendor Management:
- Evaluate and qualify suppliers and vendors to ensure quality standards are met
- Develop and execute supplier quality agreements
- Product Testing and Release:
- Oversee product testing from raw materials to finished products, ensuring they meet quality specifications
- Authorize the release of product batches after thorough quality review
- Risk Management:
- Develop and execute risk management strategies to mitigate potential quality-related issues
- Lead risk assessment initiatives and implement preventive measures
- Training and Development:
- Organize training programs on quality standards and compliance for staff
- Ensure teams are updated with the latest industry regulations and best practices
- Continuous Improvement:
- Lead quality-related projects and initiatives to enhance product quality and operational efficiencies
- Analyze quality metrics and KPIs to support strategic decision-making
Qualifications:
- Bachelor’s degree in Chemistry, Microbiology, or a related field. Master’s preferred.
- Minimum of 7 years of experience in quality assurance within supplement or pharmaceutical manufacturing
- Proven leadership experience with strong communication and problem-solving skills
- In-depth knowledge of cGMP, FDA, and industry regulations
Work Environment:
- Office & manufacturing setting within a manufacturing facility
- Full-time, in-office position
Equal Opportunity Employer Statement:
We are an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Job Types: Full-time, Part-time, Contract
Pay: $82,422.00 - $85,000.00 per year
Schedule:
- 8 hour shift
- Monday to Friday
Work Location: In person
Salary : $82,422 - $85,000