We’re seeking a Quality Specialist to support a manufacturing company’s quality team. This temporary position offers an opportunity to contribute to ongoing process improvements and compliance initiatives while working on-site in a dynamic environment. Candidates should be prepared to engage in quality assurance activities, uphold regulatory standards, and assist in various improvement projects.Quality Specialist Responsibilities:Ensure adherence to industry standards, including ISO 13485 and FDA regulations, through regular audits and process oversight.Analyze quality data to identify trends, root causes, and opportunities for improvement.Support and prepare for internal and external audits, ensuring compliance with regulatory requirements.Help manage nonconforming materials and oversee corrective and preventive actions.Train manufacturing and quality personnel on proper procedures and quality tools.Quality Specialist Qualifications:Bachelor's degree in a technical or engineering discipline.A minimum of three years' experience in a manufacturing setting, ideally within medical device or regulated industries.Strong knowledge of ISO 13485 and FDA/QSR regulations.Familiarity with quality tools such as Six Sigma, Lean, Excel, Word, and Minitab.Excellent communication skills and the ability to work independently in a fast-paced environment.Perks and Benefits:Medical, Dental, and Vision Insurance.Life Insurance.401(k) Program.Commuter Benefit.eLearning and Ongoing Training.Education Reimbursement.Eligibility requires working over 30 hours per week on an assignment lasting at least 10 weeks.If you meet the qualifications and are excited about this opportunity, apply today! Our team will connect with you to discuss next steps, support you through the interview process, and advocate for your success.