Regulatory Affairs Specialist

Actalent

Quivira, Johnson County$103,073 - $103,073 est.Full-timePosted 9h ago
Regulatory Affairs Specialist / QA-RA Lead Job Description This role leads key Quality Assurance and Regulatory Affairs activities to maintain and continually improve the Quality Management System (QMS) for a medical device organization. The position supports preparation for MDSAP certification, drives international regulatory registrations, and ensures ongoing compliance with ISO standards, FDA Quality Management System Regulation (QMSR), and other global regulatory requirements. The Regulator…

The average job posting receives 250 applications.

Stand out by tailoring your resume to this specific role. Our AI resume builder highlights the skills and experience that matter most to this employer.

Frequently asked questions

Who is hiring for Regulatory Affairs Specialist at Actalent?+
Actalent is actively hiring for this Regulatory Affairs Specialist role. Click "Apply Now" to submit your application directly on Actalent's careers page — Careeronaut doesn't charge employers or candidates for referrals.
When was this Regulatory Affairs Specialist role posted?+
This listing was first posted on 2026-07-28. We pull the latest copy from the source feed daily, and any role that's taken down gets removed from Careeronaut within seven days so you don't waste time on stale listings.
How should I apply to this Regulatory Affairs Specialist role?+
Start by tailoring your resume to the posting — most applicants send generic CVs and the first filter recruiters use is keyword relevance. Careeronaut's AI does this automatically: paste the job description, get a matched resume in under a minute, and download as PDF or DOCX.
Where can I find more Regulatory Affairs jobs in Quivira?+
Browse all open regulatory affairs roles in Quivira on the listing pages linked below. You can filter by salary, remote-friendly, and posting date.