QC Incoming Supervisor

Cytiva • Other US Location

Company

Cytiva

Location

Other US Location

Type

Full Time

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 Supervisor has direct responsibility in managing the work of QC Specialists in sampling, testing, monitoring of clean rooms, and inspecting incoming raw materials and finished products to established quality specifications. The QC Supervisor ensures that all associates carry out QC processes by closely following the standard operating procedures as they relate to materials handling, test equipment operation, Good Documentation practices, and ensuring 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:

  • Manage the execution of the daily, weekly, and monthly forecasted Quality Control priorities required to meet projected test lead times and group performance goals.
  • Coordinate the organization of personnel and equipment to ensure all QC inspections and testing meet established timelines.
  • Ensure Data Integrity and cGMP compliance within the QC laboratories and offices.
  • Provide leadership and coaching to QC associates.
  • Continuously evaluate the resource needs of the QC Raw Material inspection process and provide recommendations to the business for resource needs.

The essential requirements of the job include:

  • Bachelor's degree or significant laboratory experience (10+ years) in a GMP laboratory
  • Strong aptitude for organization and strategic thinking
  • Demonstrated ability to lead a team to deliver results to established timelines
  • Demonstrated collaboration, negotiation, and conflict-resolution skills
  • Strong aptitude in MS Office, Teams, Outlook, Word, and Excel.

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

  • 3+ yrs. of related Quality Control laboratory management experience.
  • Strong scientific background in Chemistry and/or Biological sciences.

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 [email protected] to request accommodation.

Apply Now

Date Posted

10/05/2024

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