Quality Technician

Quality TechnicianTekberry is looking for a highly qualified and motivated Quality Technician to work on-site/remotely with our client, a top-tier Dental company - the world’s largest manufacturer of professional dental products/technologies. As a W2 employee you will have access to health benefits.Responsibilities:Ensuring that products or services meet established quality standards and specifications:• Ensure that products meet established quality standards and specifications by inspecting, and verifying the quality of materials, components, and finished goods to maintain consistency and adherence to quality assurance protocols.• Inspect product at various stages in the distribution process (eg. inbound, outbound, returns)• Verify that products meet specified quality standards, tolerances, and performance criteria.• Document and report defects, deviations, or non-conformities and suggest corrective actions.• Monitor and enforce compliance with quality control policies and procedures.• Collaborate with teams within 3PL and other stakeholders to address quality issues.• Analyze and interpret quality data, identifying trends and areas for improvement.• Conduct visual inspections and measurements to check product dimensions and aesthetics.• Participate in the development and implementation of quality control processes and training programs. Maintain regulatory and quality systems to ensure the division’s compliance with FDA regulations, Corporate RA/QA and divisional requirements.• Build strong relationship with manufacturers, 3PL, and spoke warehouse personnel to implement successful change control system. Monitoring/feedback of spoke warehouses • Facilitate continuous improvement and process optimization initiatives• Root cause analysis and risk assessment• Recall support (SCI Reports) • Assist with corrective action process for all aspects of the CAPA (Corrective and Preventative Action). Assist with Quality System/GMP training to comply with FDA requirements.• Maintain training metrics to ensure that FDA requirements are followed.• Assist with the planning of all internal GMP training.Qualifications:· Ability to read, write and communicate effectively in English.· Basic computer skills required, mainly for data entry. Ability to use Microsoft Office programs as applicable.· Knowledge of Good Manufacturing Practices (cGMP).· Previous QC/QA experience in medical device or similar industry is preferred.· Familiarity with sampling plans (ANSI, AQL, etc.) is preferred.· Ability to work in a fast-paced environment with limited supervision.High School Diploma or GEDTekberry Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected categories under all applicable laws.Tekberry, Inc is a Certified Minority Business Enterprise (MBE) and Certified Disadvantaged Business Enterprise (DBE).