Helen of TroyNASDAQ: HELE: Designs and markets branded consumer housewares and personal care products.
2+ YOEHigh school degree; 5+ years consumer-relations complaint handling or 2+ years regulatory adverse event reporting; familiarity with FDA/CPSC/MDR reporting, complaint management, SOPs, and audits; authorized to work in the U.S.
Commonwealth of Massachusetts: Providing public services and governance to the people of Massachusetts.
4+ YOEBachelor's degree and 4+ years professional educational experience; ability to analyze complaints, conduct investigations, provide technical assistance, strong writing and interpersonal skills, cultural competence, travel across the Commonwealth.
HologicNASDAQ: HOLX: Develops medical technology for women's healthcare and diagnostics.
0+ YOEBachelor's degree required, 0-1 years related device or healthcare experience, knowledge of 21 CFR requirements, complaint processing, MDR reporting, and proficiency with MS Access and Excel.
Director, Policy, and Compliance (Supervisory Equal Employment Specialist)
Washington or Salt Lake City or Seattle or Phoenix or Los Angeles or San Francisco or Denver or Miami or Atlanta or Chicago or Indianapolis or New Orleans or Boston or Minneapolis or Kansas City or Albuquerque or New York or Oklahoma City or Portland or Austin
$148k-$197k/yrHybridFull Time
Department of Veterans Affairs: Federal agency providing healthcare and benefits to military veterans.
1+ YOERequires U.S. citizenship and one year of specialized experience equivalent to GS-14 in EEO policy, compliance, complaint processing, reporting, legal analysis, and program leadership.
WHOOP: Wearable technology for personalized health and performance tracking.
2+ YOEBachelor's in engineering or life sciences,2+ years QMS/QA experience in medical device or digital health,working knowledge of ISO 13485 and 21 CFR Part 820,QMS processes (CAPA,complaints,audits),and eQMS experience.
Post Market Surveillence Senior Complaints Specialist-Medical Device #7815
Marlborough, Massachusetts, United States
OnsiteContract, Full Time
ECI: Provides regulatory and engineering consulting for life sciences companies.
5+ YOEBachelor's in engineering or scientific field,5+ years medical device complaint/quality/regulatory experience,knowledge of FDA 21 CFR 820/803 and ISO 13485,experience with QMS/databases,and strong investigation and documentation skills.