Job Summary
Key Responsibilities include managing quality aspects, providing guidance on design control best practices and driving a culture of compliance and continuous improvement.
* Ensure projects are executed in accordance with relevant regulations, international standards and enterprise procedures.
* Identify and support the use of improved quality practices by R&D teams during design control activities.
* Report on project progress, identify successes and drive compliance.
* Elevate quality-related issues to the Director as required.
Qualifications:
* Bachelor's Degree in Chemistry, Engineering or Quality discipline.
* 5 years working in high-volume manufacturing environment preferably in Medical Device/Pharmaceutical sectors.
Expectations:
* Review and approve relevant documents.
* Support design transfer activities for commercial readiness and sustainment.