IQC-RGT Associate 1

POSITION SUMMARY: Support the activities for reagents used in the Operations Department’s Clinical Laboratories, which includes but is not limited to incoming material inspections to assure product safety and compliance to specifications, GMP’s, and ISO requirements. Non-technical role. PRIMARY RESPONSIBILITIES: Perform incoming inspection and reagent release: Receive, verify, label, store reagents according to department procedures Ensure equipment and instruments are in good operating condition Verify that data is properly entered into the Laboratory Information Management System Work intra and inter-departmentally to support workflows Work cross-functionally with Team and other departments on various platforms Follow/Ensure GLP (good laboratory practices) and GMP (good manufacturing practices) compliance Escalate Non-Conformity Participate in Continuous Improvement Projects Assist in training/implementation of new process changes Assist in planning workflow and day-to-day schedule Conduct self in a Professional manner Able to perform work with little to no supervision Perform other duties as assigned Adhere to Departmental Expectations This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire Must maintain a current status on Natera training requirements ​ QUALIFICATIONS: High School Diploma or GED or equivalent KNOWLEDGE, SKILLS, AND ABILITIES: Adaptability and Flexibility in a frequently changing environment Able to multi-task and work independently in a fast-paced Team environment Excellent interpersonal, communication, computer (MS word, Excel, PowerPoint, etc.), troubleshooting, organizational, problem-solving, and technical skills Strong time management skills Actively seeks ways to improve quality and workflows Willingness to learn Ability to promote a positive Team environment Maintain a high level of professionalism and responsibility Basic knowledge in Data management, Google Docs, LIMS, and Continuous Improvement Take initiative and ownership of projects/assignments with attention to detail Accept and incorporate feedback Punctual and consistent attendance Ability to speak, read, and write in English The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations. Austin, TX $18.17 — $22.74 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management. WHAT WE OFFER Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k