Wondering what's within Beckman Coulter Diagnostics? Take a closer look.At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges.The Quality Control Technician for Beckman Coulter Diagnostics is responsible for providing technical support to internal Beckman Diagnostics Quality Control (QC) organization by diagnosing, troubleshooting, repairing, and debugging complex electro/mechanical instrumentation and/or instrument computer systems. Shift is Monday - Friday, 7am - 3:30pm.This position is part of the Quality organization located in Hialeah, Fl. and will be onsite. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.You will be a part of the Hematology Quality Control team and report to the Manager Quality Control responsible for managing the hematology and microbiology laboratories. If you thrive in an amazing, fast paced, supporting role and want to work to build a world-class Manufacturing Quality organization-read on.
In this role, you will have the opportunity to:- Conducts service, repair and/or installation of instrumentation at internal QC laboratory, including electrical and mechanical testing, in accordance with service maintenance requirements.
- Executes testing, sampling, and inspection procedures for raw materials, in-process materials, and/or finished products to ensure that product specifications and company/regulatory requirements are met.
- Responsible for data review of quality control tests to ensure product specifications are met and supports investigations and troubleshooting for functionality and performance problems.
The essential requirements of the job include:- Associate in science degree with a minimum of 1 year experience working in medical device.
- Experience in Good documentation practices, Good Manufacturing Practices (GMP) and Good laboratory practices (GLP)
- Must be able to lift up to 25 pounds
It would be a plus if you also possess previous experience in:- Regulatory knowledge (FDA, World Health organization, etc.)
This job is also eligible for bonus/incentive pay.We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.For more information, visit www.danaher.com.Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at [email protected] to request accommodation.