Quality Inspector

Saltera HR is proud to partner with a medical device manufacturing organization operating in a clean, high-precision environment where quality is non‑negotiable. The Quality Inspector plays an essential role in ensuring that every product leaving the facility is safe, compliant, and built to the exact standards required for patient use. This role is hands‑on and detail focused. It is a strong fit for someone who takes pride in careful work, consistency, and doing things right the first time. What You Will Do Inspection and Quality Control Perform visual and dimensional inspections during and after production Use microscopes, calipers, micrometers, gauges, and precision measurement tools Identify and document non‑conformances and assist in root cause and corrective action processes Maintain accurate inspection logs and production records Manufacturing Support Operate and monitor production equipment to maintain accuracy and output Package, label, and prepare finished products to meet regulatory requirements Partner with Production, Quality, and Engineering on continuous improvement efforts Compliance and Safety Follow GMP, CGMP, FDA, ISO 9001/13485, and internal SOPs Maintain cleanroom standards, including proper gowning and contamination control Promote and practice safe work habits at all times What You Bring Experience in medical device or pharmaceutical manufacturing preferred Hands‑on familiarity with cleanroom work, quality inspection, and process documentation Working understanding of FDA, ISO 13485, and GMP compliance standards High attention to detail, strong communication skills, and comfort following defined procedures Mechanical aptitude and comfort learning equipment and inspection tools Basic proficiency in Microsoft Office and data entry systems What Success Looks Like Accurate, timely inspections and documentation that maintain regulatory compliance Consistent product quality with reduced non‑conformance occurrences Smooth communication between production and quality teams Active contribution to process and product improvements Work Environment Cleanroom setting with gowning requirements and strict hygiene standards Standing and performing hands‑on work for extended periods Use of microscopes and small precision instruments Climate‑controlled, structured production environment EEO Statement Saltera HR is proud to partner with organizations who value people. We support workplaces grounded in respect, safety, and equal opportunity. All qualified applicants will be considered. #J-18808-Ljbffr Saltera Group