Danaher Jobs

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 Director Filtration – Membrane sites for Cytiva is responsible for the Quality and compliance of the membrane sites and will collaborate closely with the Bioprocess Filtration business leaders on KPI priorities and strategic projects.

This position is part of the global Filtration BU Quality organisation. This position will be located in Pensacola and will be Pensacola hybrid site based . At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

In this role, you will have the opportunity to:

• Manages the Quality team of site locations in Pensacola, FL, Hauppauge, NY

• Accountable for ensuring full quality and regulatory compliance of the membrane sites through maintenance & monitoring of an ISO 9001 compliant Quality Management System .Supports New Product Development ensuring application of the Danaher Reliability System focusing on product and process quality assurance

• Facilitates in risk assessment and mitigation evaluation activities, including support to Product Managers on field action co-ordination.

• Proactively leads improvement activities linked to quality responsibility within the product life cycle management

• Reports on Quality System effectiveness and requirements to management reviews.

• Collaborates closely with Global Quality Leaders on shared priorities.

The essential requirements of the job include:

• Minimum, Bachelor's degree, preferably in a Science or Engineering field.

• A minimum of 7 years working in Quality Assurance/Quality Engineering within Life Science, Medical Device or Biopharma manufacturing environments

• A minimum of 5 years supervisory/management experience is preferred.

• Comprehensive understanding of ISO 9001 & ISO 13485 requirements. Understanding of GMP requirements, desired.

• Analytical, problem solving & root-cause analysis skills

• Experienced in managing project teams and working cross functionally, both locally & globally.

• Excellent communication skills (written and oral), fluent in English

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

• Working in a B2B industry

• Working in a global environment

• Process excellence skills

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.

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.

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 (https://www.dol.gov/agencies/ofccp/posters) .

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.