In this role, you will be responsible for ensuring that our products meet standards set by both the company and regulatory authorities. Coordinates and investigates corrective/preventive actions of the Food Safety and Quality Programs. Develops and reviews quality and safety policies and manages audits by third-party inspectors. Trains
This position will serve as a leader for Pharmacovigilance quality of all post marketing and clinical PV activities and sources in accordance with international GPvP requirements, company procedures and industry best practices.
In this role, the selected candidate will ensure that we can maintain 24/7 operations with no downtime to due quality issues, making sure the systems are operating properly and consistently, covering all testing needs.
The QC Microbiology, Associate Director oversees a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting and overseeing testing, trending, continuous improvement, and reporting of results.
The Director of Quality will wear multiple hats and oversee all of the Quality and Regulatory responsibilities. This position will start off as an independent contributor position but with the opportunity to build out a Quality team and bring the department up to where the organization needs it to be.
In this role, the individual will be responsible for providing overall direction for all quality assurance related activities associated with the China expansion project, including the following Quality workstreams; Quality Assurance, Qualification/Validation, Documentation, and
In this role, you will be responsible for developing, documenting, and administering quality and accreditation strategies, activities and programs aligned with and compliant with ArchCare Advantage Medicare Special Needs Plan.
This position is responsible for setting up the sites Quality Strategy and Quality Management System as well as oversee the Quality Assurance, Compliance, Regulatory, Quality Engineering and Continuous Improvement groups.