Quality Inspector - 2nd Shift

Elos Medtech, a leading development and production partner for medical technology companies worldwide. At our locations in Sweden, Denmark, Switzerland, Germany, China, and the USA, Elos runs operations in four business areas - Dental, Orthopedics, Advanced Surgical and Precision. Elos Medtech has extensive expertise and specializes in development and design, along with contract manufacturing of medical devices, such as implants and instruments. We are committed to meeting and exceeding our customers' high expectations. The company, headquartered in Gothenburg, Sweden, employs more than 1,500 people worldwide. In a globally growing healthcare market, we are looking for a full-time 2nd shift Quality Inspector to strengthen our team in Memphis, TN. The Quality Inspector ensures that the highest standards of quality and compliance in our medical device production are met. This role is critical to maintaining product integrity, patient safety, and regulatory compliance. Responsibilities PASSION: Demonstrate commitment to patient safety by ensuring every device meets the highest quality standards PASSION: Stay current with industry regulations (e.g., FDA, ISO 13485) and continuously seek ways to improve inspection processes PASSION: Take pride in craftsmanship and precision when inspecting components and assemblies PASSION: Perform thorough in-process and final inspections of medical devices, ensuring compliance with specifications, drawings, and regulatory standards TRUSTWORTHINESS: Maintain accurate and transparent quality control records TRUSTWORTHINESS: Ensure compliance with regulatory requirements and internal procedures TRUSTWORTHINESS: Identify and report defects or non-conformances with integrity and objectivity TRUSTWORTHINESS: Support audits by providing reliable documentation and insights DRIVE RESULTS: Perform thorough inspections using precision tools to verify product specifications DRIVE RESULTS: Support CAPA initiatives to resolve quality issues and prevent recurrence DRIVE RESULTS: Maintain and calibrate inspection equipment to ensure consistent performance DRIVE RESULTS: Meet deadlines and production goals without compromising quality COLLABORATION: Work closely with production and engineering teams to resolve quality concerns COLLABORATION: Train staff on quality standards and inspection techniques COLLABORATION: Participate in cross-functional meetings to improve processes and share best practices COLLABORATION: Communicate clearly and constructively with team members and leadership Other duties: As assigned Skills Ability to use calipers, micrometers, CMMs, optical comparators, and other precision tools Familiarity with ISO 13485, FDA, and GMP standards Accurate recordkeeping, non-conformance reporting and audit support Basic Microsoft Office skills and ERP systems Ability to train others in inspection procedures and quality standards Effective communication skills to interact with team members, production staff, and leadership Ability to work independently or collaboratively in a fast-paced manufacturing environment Flexibility to adapt to changing priorities Experience Minimum 2 years of experience in quality inspection, preferably in the medical device or regulated manufacturing industry Background working in cleanroom, GMP, or ISO-certified environments desirable Familiarity with CAPA processes, audits, and regulatory inspections Education Education: High school diploma or equivalent Physical Demands Ability to stand or sit for extended periods while performing inspections Frequent repetitive hand and arm movements when using precision tools and equipment Must be able to lift, carry, push, and/or pull up to 20 lbs. independently; occasional lifting of heavier objects may be required with mechanical assistance or team lift Required to wear appropriate Personal Protective Equipment (PPE), including but not limited to safety glasses, gloves, protective clothing, and hearing protection as dictated by task and environment Visual acuity sufficient to conduct detailed inspections of equipment and parts, read technical documentation, and view computer screens Hearing ability sufficient to perceive alarms, equipment signals, and verbal instructions in a manufacturing environment Must be able to bend, stoop, reach, and work in confined or awkward positions as necessary to access equipment and perform maintenance tasks Working Conditions Manufacturing and cleanroom environments Standard schedule is Monday-Friday on first shift, weekend work as needed Reporting Structure This position reports to the Value Stream Supervisor #J-18808-Ljbffr