Quality Assurance Specialist

Quality & Regulatory Affairs SpecialistThe Quality & Regulatory Affairs Specialist will support the Q&RA Management team in ensuring compliance to regulations and standards and meeting customer requirements.Responsibilities:Assist Q&RA Management with:Development and revision of quality process documentation (SOPs, work instructions, forms & templates)Documenting and following up on events (Nonconforming material, CAPA, audit findings, etc.)Internal Auditing of the QMSQuarterly Trending of DataTraining activitiesOther Duties as assignedRequired Qualifications:2-5 years' experience in a Quality and Regulatory role (preferred Medical Device manufacturing)Experience with ISO 9001 or 13485Experience generating and revising QMS documentationMicrosoft Office Suite ProficientManage multiple assignments simultaneouslyExcellent written and verbal communication skillsAdditional Information:As a full-time team employee, you are eligible for all RbM Services benefits, including medical, dental, vision, long-term, short-term disability, 401k, PTO, 10 paid holidays, etc.All your information will be kept confidential according to the EEO guidelines