Responsible for building and leading cross-functional quality assurance systems across Loyal teams with an emphasis on FDA-CVM regulatory compliance for drug submissions and products. The work will ensure that all aspects of drug development, manufacturing and clinical operations are high quality, and that any deviations from this are investigated and understood. The Quality Compliance Officer is responsible for maintaining and continuously improving the companyβs Quality Management System (QMS) to ensure compliance with applicable regulations, standards, and internal policies.
This role oversees the development, implementation, and management of Standard Operating Procedures (SOPs), company-wide training programs, and quality compliance activities that support operational excellence and regulatory readiness. This role ensures that in house and external programs are executed to an appropriate quality standard and also to ensure that appropriate quality systems are implemented.
Design a Quality Assurance Unit program and system that is fit for purpose in the current company and can scale to a foreseeable future, while being a kind and considerate team member, especially where quality reviews make life harder for collaborating teams in house.