Job Description
The role of the Medicines Quality Organisation is to support the development and implementation of quality systems strategy and activities. This includes integrating quality requirements into business processes, implementing quality plans, and ensuring consistency between global and local requirements.
Key responsibilities include managing quality systems, providing quality oversight for business areas, conducting audits and inspections, partnering with other areas, and performing other responsibilities such as understanding confidential information handling and EU Qualified Person for Pharmacovigilance (EU QPPV) roles.
Required Skills and Qualifications:
A Bachelor's or Master's degree in a science or health care related field, Health care professional, such as Pharmacist, Nurse. Three years experience in quality and/or drug product safety/regulatory. Demonstrated ability to implement, interpret and apply quality systems within a regulated work environment. Cognitive abilities which include problem solving, verbal reasoning, attention to detail, critical thinking and analytical competencies. Demonstrated ability to communicate effectively, both written and verbal, and to influence others. Demonstrated ability to prioritise and handle multiple concurrent tasks. Demonstrated ability to apply risk-based decision making in a regulated environment.
Benefits
Competitive salary and benefits package. Opportunity to work in a global environment with cultural sensitivity. Dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. No discrimination on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Others
Support key projects as assigned. Perform quality self-assessments, as needed.