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Danaher Corporation QC Specialist - 2nd Shift in Logan, Utah

Help us improve access to life-changing therapies that can transform human healthWe are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.We are looking for a MICROBIOLOGY QC SPECIALIST to work with our expert Quality Control team of 50 employees across the world. Do you have a passion for Quality? Then we would love to hear from you.What you’ll do

  • Maintenance of QC testing laboratory operations and supporting quality records in line with GLP.

  • Be involved in data analysis & technical report writing.

  • Assist as needed for improving existing test methods

  • Participate in continuous improvement activities by identifying and appropriately escalating process and product quality gaps, providing solutions when possible.

  • Accountable for the on-time delivery of data in support of in-process, release and stability activities.

  • Ensure documentation data integrity and GMP compliance requirements are followed within the laboratories

  • Compliance with site Quality Management system requirements

  • Maintaining high housekeeping and safety standards.

Who you are

  • A HS diploma or GED plus laboratory experience is required. A degree or pursuing a degree in Biology, Chemistry, Biotechnology is preferred.

  • Experience or knowledge of working in a clean room environment preferred

  • Excellent communication (written & verbal) & technical reporting skills

  • Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures)

  • Demonstrated ability to solve problems, develop plans and advance to completion on time and in full.

  • Willingness to participate and learn in a strong continuous improvement and safety culture

  • Demonstrated collaboration & conflict resolution skills within a team environment

  • Ability to multi-task & handle tasks with competing priorities effectively

  • Proficient in the use of IT systems & Microsoft applications (Outlook, Excel, Word, PowerPoint)

Who we areWhatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!Cytiva is a global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .