Quality Assurance Manager
3 weeks ago
About Our Company
">RbM Services, a trusted partner in the medical device industry, offers a unique opportunity for a Quality & Regulatory Affairs Specialist to join our team.
">Job Summary
">As a Quality & Regulatory Affairs Specialist, you will be responsible for supporting the Q&RA Management team in ensuring compliance to regulations and standards and meeting customer requirements.
">Key Responsibilities
">- ">
- Develop and maintain quality process documentation (SOPs, work instructions, forms & templates).">
- Investigate and document events (Nonconforming material, CAPA, audit findings, etc.).">
- Conduct internal audits of the QMS.">
- Collect and analyze data quarterly.">
- Train and educate colleagues on quality processes.">
- Perform other duties as assigned.">
Requirements
">- ">
- At least 2-5 years experience in a Quality and Regulatory role (preferably in Medical Device manufacturing).">
- Familiarity with ISO 9001 or 13485.">
- Experience in generating and revising QMS documentation.">
- Strong computer skills with proficiency in Microsoft Office Suite.">
- Able to multitask and prioritize assignments.">
- Superior written and verbal communication skills.">
Compensation Package
">$70,000 - $90,000 per year, depending on qualifications and experience, plus comprehensive benefits package.
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