What are the responsibilities and job description for the Validation and Quality Systems Manager position at CSBio?
Career Advancement:
As the Associate Director, Quality Assurance, you will have the opportunity to lead cross-functional teams and make significant contributions to the company's success.
About the Role:
This is an exciting opportunity to join CSBio's leadership team and drive quality and compliance initiatives across the organization.
Responsibilities:
- Develop and implement quality management systems to ensure compliance with regulatory requirements
- Lead audits and inspections to ensure readiness and effectiveness
- Develop and maintain training programs to support employee development and compliance
Qualifications:
- Bachelor's degree in a relevant field (e.g., engineering, life sciences)
- Minimum 8 years of experience in quality assurance with at least 4 years of experience in managing validation and quality systems
- Strong understanding of GMP and regulatory requirements (ICH and FDA)
