Minnesota Jobs
Quality Assurance Specialist
Are you passionate about quality and ready to make an impact in the medical device industry? Staffmark is partnering with a respected manufacturer in Chanhassen, MN to hire a Quality Assurance Specialist. This is a great opportunity to bring your expertise to a collaborative, high-performing team where your skills directly contribute to product safety and compliance. Pay: $35 - $40 per hour Schedule: Monday - Friday | 8:00 AM - 4:30 PM What You'll Do: Ensure quality compliance with FDA, ISO 13485, MDSAP, and MDD/MDR standards Collaborate with Engineering and Quality teams during product development Support risk management, post-market surveillance, and regulatory submissions Perform data entry, analysis, and audit support (internal and third-party) Investigate complaints and participate in CAPA processes Track and report quality data for management review What We're Looking For: Bachelor's degree in Engineering, Medical Device, or related field 2+ years of Quality experience in the medical device industry Familiarity with FDA, ISO, MDSAP, and MDR/MDD regulations Strong analytical, organizational, and communication skills Proficiency in Microsoft Office and Adobe Why You'll Love This Job: Our partner company can provide you with the vital benefits that you deserve. A list of benefits will be provided to you upon hire.
Are you passionate about quality and ready to make an impact in the medical device industry? Staffmark is partnering with a respected manufacturer in Chanhassen, MN to hire a Quality Assurance Specialist. This is a great opportunity to bring your expertise to a collaborative, high-performing team where your skills directly contribute to product safety and compliance. Pay: $35 - $40 per hour Schedule: Monday - Friday | 8:00 AM - 4:30 PM What You'll Do: Ensure quality compliance with FDA, ISO 13485, MDSAP, and MDD/MDR standards Collaborate with Engineering and Quality teams during product development Support risk management, post-market surveillance, and regulatory submissions Perform data entry, analysis, and audit support (internal and third-party) Investigate complaints and participate in CAPA processes Track and report quality data for management review What We're Looking For: Bachelor's degree in Engineering, Medical Device, or related field 2+ years of Quality experience in the medical device industry Familiarity with FDA, ISO, MDSAP, and MDR/MDD regulations Strong analytical, organizational, and communication skills Proficiency in Microsoft Office and Adobe Why You'll Love This Job: Our partner company can provide you with the vital benefits that you deserve. A list of benefits will be provided to you upon hire.