Seeking a dynamic professional to join our team as a Value Stream Interface Expert.
About the Role
* This is an exciting opportunity for someone with a strong background in regulatory affairs and quality assurance to take on a challenging role within the IC Value Stream (VS) Interface department.
The ideal candidate will have excellent project management skills, a deep understanding of quality management and risk management standards, and experience working with medical devices and medicinal products.
Key Responsibilities
The successful candidate will be responsible for managing the VS interface activities, developing and deploying performance metrics, and ensuring compliance with regulatory requirements.
In this role, you will also be responsible for establishing standardized global VS expectations, supporting the implementation and maintenance of a regulatory information management system, and collaborating with stakeholders to create a harmonized document management structure.
Requirements
* Advanced knowledge of quality management and risk management standards (e.g., ISO13485, ISO14971).
* Experience in project management and a strong understanding of regulatory affairs.
* Excellent communication and collaboration skills.
A minimum of 5+ years' experience in the field of Regulatory or Quality Assurance Medical Devices / Medicinal Products is required. If you are a motivated and results-driven individual with a passion for regulatory affairs and quality assurance, we encourage you to apply for this exciting opportunity.
Benefits
We offer a competitive compensation package, opportunities for career growth and development, and a dynamic work environment that fosters collaboration and innovation.
Others
Please submit your application, including your resume and a cover letter outlining your relevant experience and qualifications.