Regulatory QA Specialist - FDA Submissions & Audits
CAIRE
CAIRE is seeking a QA/RA Specialist in Ball Ground, GA. In this full-time role, you will collaborate with the FDA and regulatory bodies on submissions and audits. You'll ensure compliance and maintain the quality management system. The ideal candidate holds a Bachelor's degree and possesses strong communication skills, able to manage multiple projects effectively. This position requires minimal travel and operates in a professional office and manufacturing environment. #J-18808-Ljbffr CAIRE
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Regulatory QA Specialist - FDA Submissions & Audits in Ball Ground, GA vacancy
- ...based in Ball Ground, Georgia, is seeking a Quality Assurance & Regulatory Affairs Specialist. In this role, you will work with the FDA and international regulatory bodies on product submissions and audits. Your responsibilities include ensuring product compliance with...Suggested
- ...alternative application process. QA/RA Specialist Full Time Individual Contr. Ball... ...GA, US As a Quality Assurance & Regulatory Affairs Specialist, you will work with the FDA and international regulatory bodies on product submissions, audits, and event reporting. You will...SuggestedFull timeWork experience placementInternshipWork at officeLocal area
- ...include, but are not limited to: delivery of technical training to instrument techs, performance and documentation of quality assurance audits, TJC and AAMI compliance, orientation of newly hired instrument techs, promoting certification activities throughout the department...SuggestedShift workWeekend work
- ...include, but are not limited to: delivery of technical training to instrument techs, performance and documentation of quality assurance audits, TJC and AAMI compliance, orientation of newly hired instrument techs, promoting certification activities throughout the department...SuggestedShift work
- ...sterile processing. The role involves implementing the department's improvement initiatives, technical training, and conducting quality audits. Ideal candidates will have at least two years in sterile processing, hold a CRCST or CSPDT certification, and possess skills in...SuggestedAfternoon shift
- ...program within the department. Key duties include delivering technical training to instrument technicians, performing quality assurance audits, ensuring TJC and AAMI compliance, and supporting new hires' orientation. Preferred qualifications include an Associate's degree...
- ...involves inspecting products, analyzing data, and ensuring compliance with quality standards. You will handle complex issues, conduct audits, and use various tools like calipers and micrometers in your daily work. A background in ISO procedures and ASQ certification is...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory QA Specialist - FDA Submissions & Audits. Be the first to apply!

