We are seeking an experienced RAQA Manager to lead regulatory affairs and quality assurance for a medical device organization. The role involves ensuring product safety, compliance, and functionality, managing QA/RA systems, optimizing processes, and leading a high-performing team. The ideal candidate has extensive experience in medical device QA/RA, strong leadership skills, and a strategic, business-minded approach.
Key Responsibilities:
Lead and manage QA and RA teams, including training and succession planning.
Ensure compliance with global and local medical device regulations.
Implement and maintain QMS, GVP, and product introduction/change processes.
Collaborate with suppliers, manufacturing partners, and stakeholders to maintain product quality.
Drive process improvement, risk management, and strategic initiatives.
Frequently asked questions
Who is hiring for the RAQA Product Development Associate Director role?
Tardis Group is hiring for the RAQA Product Development Associate Director position, a Shazamme client. Apply directly on the employer's career site.
Where is the RAQA Product Development Associate Director job located?
The RAQA Product Development Associate Director role with Tardis Group is based in Tokyo, JP.
Is the RAQA Product Development Associate Director role full-time or contract?
This is a full time position at Tardis Group.
What experience level is the RAQA Product Development Associate Director role?
The RAQA Product Development Associate Director position is aimed at director-level candidates.
How do I apply for the RAQA Product Development Associate Director role at Tardis Group?
Apply directly on Tardis Group's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.