QA/RA Manager
San Diego, San Diego County, California, 92189, USA
Listed on 2026-01-10
-
Quality Assurance - QA/QC
Data Analyst
This range is provided by CSG Talent. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range$/yr - $/yr
Direct message the job poster from CSG Talent
Global Headhunter - Critical Care equipment/devices & Hospital Integration/Connectivity at CSGQuality and Regulatory Affairs Lead
Salary/bonus:
Up to $170,000 fixed plus bonus
Based:
South California
Are you a proven quality and regulatory specialist where a fast track career move could interest you?
Would a role leading an entire N American quality and regulatory function, one that boasts a lot of opportunities for fast professional and personal growth?
CSG are proudly and exclusively partnering a global innovation leader in the acute/critical care equipment and devices space (predominantly Class II), operating in a life saving, high value and highly technical area of integrated hospital solutions.
The business is at an exciting point, growth mode and as a result are looking for an experienced Snr Quality and Regulatory Manager to join their USA Team. The business are again a global manufacturer and innovation leader, with direct manufacturing operations in the USA.
Key Responsibilities:
- Establish the strategy for all USA Regulatory and Quality Assurance activities Current account retention and growth, leading the implementation of entire USA QA/RA strategy
- The position will be involved in all phases of the complete line of products to ensure timely initial 510(k) clearance and compliance until end of the products commercial life cycle
- Will develop and maintain external relationships with key individuals and agencies that play critical roles in the FDA clearance process for all products, leading and direct high-quality, well-organized FDA submissions for new and existing products.
- Oversees all aspects of US based Quality Management System, specifically CAPA, Complaint and QMS compliance
Key Requirements:
- A proven track record in Quality Assurance and Regulatory Affairs across the USA in Med Tech
- FDA management and 501(k) submissions experience with Class II devices
- Class II devices experience is essential, we cannot consider anyone without extensive experience in this area
- Quality Management Systems, CAPA and Post Market Surveillance experience
- The ability and experience to own and drive the entire QA/RA USA function independently
- USA citizen with the legal right to work in the USA without sponsorship
- Flexibility to regularly present in the office and manufacturing site in S California
If the above is fits your experience and approach to sales/business development please apply and I will be in touch to discuss. Just as an immediate disclaimer I can only consider people who fit the exact description above, if you apply and don't fit the specification unfortunately I will not be able to consider you.
CSG Talent are an equal opportunities employer working on behalf of the client.
Seniority level- Seniority level
Entry level
- Employment type
Full-time
- Job function
Quality Assurance - Industries Medical Equipment Manufacturing
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