About Your New Role:
Key Responsibilities
You will support the production of life-saving therapies for global pharma clients. You will work collaboratively with subject matter experts to drive quality improvements and deliver QA objectives.
The role requires collaboration with commercial and technical operations teams to drive business growth and develop innovative solutions. Key performance indicators tracking, metrics reporting, and corrective actions implementation are also part of your responsibilities.
You will be responsible for identifying value-added improvements, reviewing open actions related to Corrective and Preventative Actions (CAPA), Out of Specification (OOS) reports, and Deviations. Hosting Client quality audits, including addressing findings and required actions, is another important task.
Managing the Internal Audit program, coordinating audit schedules, reviewing findings, tracking corrective actions, and driving continuous improvement are part of your key responsibilities.
Requirements
The ideal candidate should have a minimum 3 years of professional experience in the pharmaceutical industry in a Quality Assurance-focused role. Integration with organizational Core Values, culture, and team climate is essential.
You should be detail-oriented, able to focus on details while understanding the overall direction. Self-motivated, identifying what needs to be done and doing it proactively is also important.