Product Release Quality Assurance Associate… at MicroPort · Arlington

PRODUCT RELEASE QUALITY ASSURANCE ASSOCIATE OR TECHNICIAN (1ST SHIFT) Ready to join our team? Apply today! Make sure to check your email for follow-ups.   At MicroPort, we relentlessly strive to master every detail of our medical solutions with the purpose of prolonging and reshaping the lives of patients everywhere. We welcome motivated and talented people who want to join our dynamic and inclusive company, working together to deliver meaningful medical breakthroughs. In order to accomplish this, we hold true to our core values of Quality, Integrity, Accountability, Efficiency, Innovation, Aspiration, Dedication & Collaboration. Come and join Team MicroPort!     Why You’ll Love MicroPort You will find our team atmosphere challenging and rewarding. In addition to working with a world-class team, receiving a competitive base salary and bonus opportunities, our U.S. employees also enjoy the following benefits: Medical, Dental, Vision, Maternity Leave, Life Insurance, Short-Term Disability, Long-Term Disability, Bereavement, 401(k) (up to 4% match with vesting from day 1), PTO, Employee Assistance Program, Education Assistance...and more! At MicroPort, we care about our employees and encourage them to make healthy lifestyle choices and embrace wellness opportunities to maintain their very best health and wellbeing.   Overall Summary As Product Release Quality Assurance Associate or Technician, you will perform documentation review to all device history, associated data, and documentations prior to releasing product. You will ensure products are not available for release until ambiguities and errors are resolved.  Authorized person(s) shall issue the product release form as required and approve the release of the finished product, while remaining independent of other functions such as, but not limited to production and inspection.   This is a 1st shift position: 7:00am-3:30pm, Monday-Friday   Your duties will include: 1. Assure inspection is performed in accordance with FDA, ISO, and other applicable regulations / guidelines. 2. Follow written instructions with engineering-based content. 3. Apply attention to detail in documentation. 4. Interface with peers, engineers, and Regulatory auditors. 5. Accurately record data results to ensure proper segregation of accepted and rejected products. 6. Operate under the direction of QC Management team. 7. Develop, update, and maintain Device History Record database 8. Provide Certificate of Conformance (CoC) upon request Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.      About You   We might be a great match if you have: ·         ABILITY TO FOLLOW INSTRUCTIONS, BOTH WRITTEN AND ORAL. ·         ABILITY TO WORK IN A TEAM ENVIRONMENT. ·         PROFESSIONAL COMMUNICATION SKILLS. ·         A WORKING KNOWLEDGE OF BASIC COMPUTER SKILLS ·    ABILITY TO APPLY SKILLS IN A MANNER TO ENSURE PROPER DECISIONS FOR ACCEPTANCE OR REJECTION OF GOODS IS IMPERATIVE. ·         DATABASE MANAGEMENT KNOWLEDGE ·         ABILITY TO WORK INDEPENDENTLY     YOUR EDUCATION Required: High School Diploma or GED Preferred: High School Diploma   YOUR EXPERIENCE Associate: No related experience required Technician: One year of related experience required    Visual acuity requirements apply to the role, including peripheral, color, and depth perception.   For internal reference, the Associate is a level H2, and the Technician is a level H3.