Are you a meticulous and detail-oriented individual with a passion for ensuring product quality and compliance? Do you have an understanding of quality management systems and a desire to contribute to a growing organization? We are seeking a dedicated QA/QC Specialist to join our Quality team at our headquarters in Pompano Beach, FL.In this onsite role, you will be instrumental in performing quality inspections of incoming materials, in-process goods, and final products. You will also play a key role in maintaining our Quality Management System (QMS) and driving continuous improvement initiatives to ensure the highest quality in our products.Qualifications: Associate’s degree or a minimum of 2 years of relevant experience in the quality field. A Bachelor’s degree is strongly preferred.Demonstrated experience using various inspection equipment and maintaining detailed inspection documentation (e.g., calipers, pin gages, scales, sampling plans, inspection forms and records).Practical experience working with ISO 14971 compliant risk files and/or training in the ISO 14971:2019 Risk Management standard.Proven working knowledge of 21 CFR 820, ISO 13485, and current Good Manufacturing Practices (cGMP).Prior experience in the medical device industry and/or cleanroom environments is considered a significant advantage. salary: $62,000 - $65,000 per yearshift: Firstwork hours: 8 AM - 5 PMeducation: AssociateResponsibilities Conduct thorough inspections of raw materials and finished goods, meticulously documenting findings in accordance with established material and document control procedures.Interpret technical drawings, specifications, and work instructions to accurately assess product quality against defined expectations.Maintain exceptional attention to detail while performing inspections and recording results to ensure accurate identification, traceability, and maintenance of device master records in compliance with company standard operating procedures.Promptly communicate any nonconforming materials to Quality management, facilitating timely investigation and documentation through the nonconforming material record process (NCMR).Perform detailed reviews of Device History Records and other quality documentation to verify adherence to established procedures and Good Documentation Practices, collaborating with other departments as necessary for clarification.Utilize an Enterprise Resource Planning (ERP) System to efficiently store quality records, execute material movement and control transactions, and verify critical product information. Skills Quality ControlProduction ControlProduct InspectionTestingMonitoringQuality AssuranceInspectionSupervisingBasic Software SkillsSamplingReassembly Qualifications Years of experience: 2 yearsExperience level: Experienced Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).This posting is open for thirty (30) days.