Quality Engineer (USC/GC)

Quality Engineer (USC/GC) Data Base Solutions Private Limited Memphis, TN Job Details Full-time | Contract $35 - $39 an hour 14 hours ago Benefits 401(k) Qualifications Statistical software Statistics ISO certification process Compliance audits & assessments GMP Project management in manufacturing Analysis skills Medical device manufacturing facility experience HACCP Attention to detail Regulatory/legal compliance standards in production Biomedical regulatory compliance Managing projects Quality audits Cross-functional collaboration Production process auditing Cross-functional communication FDA regulations Statistical analysis tools Full Job Description Overview We are seeking a highly motivated and detail-oriented Quality Engineer (USC/GC) to join our dynamic team. In this pivotal role, you will champion quality assurance and control processes across manufacturing operations, ensuring products meet rigorous industry standards and regulatory requirements. Your expertise will drive continuous improvement, uphold compliance with essential standards, and foster a culture of excellence. This is an exciting opportunity for a proactive professional eager to make a tangible impact on product quality and safety. Duties Develop, implement, and maintain quality management systems aligned with

ISO 13485, ISO 9001, FDA

regulations, and other relevant standards. Conduct comprehensive quality audits to assess compliance with internal policies and external regulatory requirements. Oversee quality control procedures during manufacturing, including inspection and testing of raw materials, in-process components, and finished products. Lead root cause analysis for quality issues, implementing corrective and preventive actions (CAPA) to resolve non-conformances effectively. Collaborate with cross-functional teams to enhance quality systems, streamline processes, and ensure adherence to HACCP, CGMP, and other industry-specific protocols. Facilitate training sessions on quality standards, inspection techniques, and regulatory updates for staff at all levels. Prepare detailed reports on quality metrics, audit findings, and process improvements to support management decision-making. Requirements Proven experience working within manufacturing environments adhering to

ISO 13485, FDA

regulations, HACCP, CGMP, ISO 9001, and related standards. Strong knowledge of quality assurance (QA), quality control (QC), and quality management systems (QMS). Demonstrated ability to conduct thorough quality audits and inspections across various stages of production. Excellent analysis skills with the capacity to identify issues quickly and develop effective solutions. Project management skills with the ability to prioritize tasks in a fast-paced setting. Familiarity with QA/QC tools such as statistical analysis software and inspection equipment. Effective communication skills to collaborate with diverse teams and present findings clearly. Join us as we uphold the highest standards of quality while fostering innovation and continuous improvement! This role offers an engaging environment where your expertise directly influences product safety, compliance, and customer satisfaction. We are committed to supporting your professional growth through ongoing training opportunities in industry standards and regulatory updates.

Pay:

$35.00 - $39.00 per hour

Benefits:

401(k)

Work Location:

In person