Senior Quality Assurance / Post-market Surveillance Specialist

Position Summary

Develops and applies intermediate knowledge and understanding of the Quality Assurance frameworks, legislative requirements, processes and procedures in the EMEA distribution organization.

Responsible for developing and maintaining the effectiveness of QMS in accordance with ISO 13485:2016 standard and the applicable regulatory requirements.

Responsible for handling post-market surveillance (PMS) activities, such as Product complaints, Product Field Actions and Commercial holds.

How to apply:

Check the link below for more details about our company and the position, and to submit your application:

https://stryker.wd1.myworkdayjobs.com/StrykerCareers/job/Moscow-Russia/Senior-QA---PMS-Specialist_R527191

What you will do:

• Develop and maintain the effectiveness of local QMS in accordance with the company objectives and applicable requirements
• Maintain, develop and/or revise QMS process documentation aligned with ISO 13485:2016 standard to incorporate appropriate regulatory and EEMEA requirements
• Ensure that EEMEA procedure and document changes are reviewed and implemented where appropriate into the local QMS
• Execute QA activities in line with defined procedures and processes, such as - internal audit process, supplier management, document control, risk management, NC-CAPA and others
• Cooperate with RA specialists for timely organization and execution of manufacturing site inspections in accordance with applicable local regulations based on annual registration plan and business priorities
• Execute PMS activities, such as Product complaints, Product Field Actions and Commercial holds, in line with defined procedures and legal regulations

Requirements:

• Bachelor’ degree ideally in Engineering, Medical Device Technology or Scientific field preferable
• 2+ years’ experience in a related Quality Assurance position
• Prior experience in medical device company is desirable
• Strong IT skills, including Microsoft Office
• Russian - native speaker, English – upper intermediate
• Qualified as QMS Internal Auditor (ISO 13485 medical devices preferred)
• Project management and time management skills, coordination and execution of projects
• High attention to detail and process consciousness, proactive mindset
• Versatility, flexibility and willingness to work with changing priorities
• Strong communication and team working skills, ability to communicate effectively with the team and management
• High ethical standards and integrity