Senior Quality Engineer

Danaher

  • Pensacola, FL
  • Permanent
  • Full-time
  • 1 month ago
Bring more to life.Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?At Cytiva, one of 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.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. Take your next step to an altogether life-changing career.Learn about the which makes everything possible.The Senior Quality Engineer is responsible for ensuring the quality of membrane products through setting inspection processes, implementing quality control measures and identifying improvement areas. Additionally, the Sr. Quality Engineer addresses customer complaints, resolves production quality issues, collaborates with cross-functional teams to identify root causes, and drives continuous improvements to deliver high-quality products. Additionally, they support new product introduction projects.This position reports to the Sr. Quality Engineer Team Leader and is part of the Quality Engineering Team located in Pensacola, FL and will be an on-site role.What you will do:
  • Investigate and correct root causes of product failures occurring in the field.
  • Ensure design control process compliance throughout whole product lifecycle and deliver training on quality process guiding colleagues and team members as required.
  • Guide and overall support product risk management process.
  • Establish, maintain, monitor QMS process performance with data analysis and lead quality improvement project from system level
  • Responsible for issuing or reviewing and approving validation documents
Who you are:
  • Bachelor’s degree in science, engineering, or technical field required
  • 3+ years of relevant experience in biomedical or medical device manufacturing preferred
  • Uses analytical mind and data analysis to creatively and pragmatically solve problems, comes up with solutions
  • Extensive knowledge of quality standards ISO 9001 and ISO 13485
  • Knowledge of QMS
Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
  • Ability to travel 15 % travel, overnight, within USA and internationally
  • Must have a valid driver’s license with an acceptable driving record
  • Ability to lift, move or carry equipment up to 50lb
It would be a plus if you also possess previous experience in:
  • Root Cause analysis and Risk mitigation Experience
  • Minitab, and Microsoft Applications
  • Identifying, analyzing and mitigating risk
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at .At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.The salary range for this role is
insert range
. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.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 .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 .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 to request accommodation.

Danaher