QC Specialist 1 at Cytiva in Logan, Utah

Job Description:

Be part of something altogether life-changing!

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term.

Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.

The Quality Control Specialist has front-line responsibility in sampling, basic testing, monitoring of clean rooms, and inspecting incoming raw materials and finished products to established quality specifications. All associates carry out QC processes by closely following the standard operating procedures as they relate to materials handling, test equipment operation, and data integrity.

This position is part of the Quality Control department located in Logan, Utah and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

In this role, you will have the opportunity to:

• Ability to read and follow work policies and procedures, EHS, Quality control inspections along with schematics or receives verbal instructions regarding duties to be performed. Along with GMPs and Good documentation skills.


• Complete all planned Quality & Compliance training within the defined deadlines. Identify and report any quality or compliance concerns and take immediate corrective action as required.


• Knowledge and understanding of QC laboratory processes, work instructions, documentation configuration control, non-conforming and rework documentation requirements and operates within them to ensure that the raw materials and product conforms to its specification


• Aware of and comply with Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position.

The essential requirements of the job include:

• High School Diploma/GED or local equivalent. 2 years working experience in GMP Manufacturing or Laboratory environment​


• Ability to work well and communicate with other QC specialists, scientists, planners, supervisors, and managers to improve quality and process efficiency.


• Frequently move, climb stairs daily, lift, carry, push or pull weights up to 50 lbs. unassisted and occasionally lift/move weights greater than 50 lbs. with assistance. Along with ability to wear protective equipment including clean room gowning, chemical resistant clothing, safety glasses/goggles. Frequently squat, stoop, kneel, crouch, turn, pivot and reach. Frequently use fingers or hands to grasp, clamp, move, finger, handle and feel small objects. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, color vision, depth perception and ability to adjust and focus on objects.

It would be a plus if you also possess previous experience in:

• 3+ yrs. of related Quality Control laboratory experience.


• Some additional scientific Higher Education in a science field


• MS Office, Teams, Outlook, Word, and Excel.

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.

At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond. 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 applyassistance@danaher.com to request accommodation.