Job summary
Job post source
This job is directly from Cytiva
Job overview
The Senior Quality Engineer at Cytiva ensures membrane product quality by setting inspection processes, implementing quality control, addressing customer complaints, and supporting new product introductions to impact life sciences and biotechnology.
Responsibilities and impact
The role involves investigating product failures, ensuring design control compliance, supporting risk management, monitoring QMS performance, leading quality improvement projects, and approving validation documents.
Compensation and benefits
The position offers a salary range with potential bonus/incentive pay, comprehensive benefits including paid time off, medical/dental/vision insurance, and 401(k) plans.
Experience and skills
Requires a bachelor's degree in science, engineering, or technical field, 3+ years in biomedical or medical device manufacturing preferred, knowledge of ISO 9001 and ISO 13485 standards, QMS, and strong analytical problem-solving skills; experience with root cause analysis, risk mitigation, Minitab, and Microsoft applications is a plus.
Career development
Cytiva promotes continuous improvement and offers opportunities for professional growth through challenging projects and learning within a culture of innovation and belonging.
Work environment and culture
Cytiva fosters a culture of belonging, continuous improvement, and innovation with a commitment to diversity, equity, and inclusion, supporting flexible and remote work arrangements where eligible.
Company information
Cytiva, a Danaher operating company, specializes in life sciences, diagnostics, and biotechnology, providing solutions that support biological research, vaccine development, and advanced therapies globally.
Team overview
The Senior Quality Engineer will join the Quality Engineering Team in Pensacola, FL, reporting to the Sr. Quality Engineer Team Leader, working collaboratively on quality assurance and product improvement.
Job location and travel
This is an on-site role based in Pensacola, FL, with up to 15% travel required domestically and internationally; remote work options may be available for eligible roles.
Unique job features
The job features involvement in cutting-edge life sciences projects, use of Danaher Business System for continuous improvement, and the opportunity to impact health through quality engineering in biotechnology.
Company overview
Cytiva is a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. They specialize in bioprocessing, cell and gene therapy, and diagnostics, offering products such as filtration systems, chromatography resins, and cell culture media. The company generates revenue through the sale of these products and associated services, including training and consultancy. Originally part of GE Healthcare Life Sciences, Cytiva became an independent entity in 2020 after being acquired by Danaher Corporation. This acquisition has enabled Cytiva to expand its capabilities and market reach significantly.
How to land this job
Position your resume to emphasize your expertise in quality engineering within biomedical or medical device manufacturing, highlighting your knowledge of ISO 9001 and ISO 13485 standards and experience with QMS processes.
Showcase your skills in root cause analysis, risk management, and continuous quality improvement projects, as well as your ability to lead and support product lifecycle design control and validation activities.
Apply through multiple platforms including Cytiva's official corporate careers page and LinkedIn to maximize your application visibility and ensure you cover all potential hiring channels.
Connect with current employees in Cytiva's Quality Engineering Team on LinkedIn; start conversations by referencing recent company innovations or asking about their experience working on quality improvements in life sciences products.
Optimize your resume for ATS by incorporating keywords from the job description such as 'quality control,' 'root cause analysis,' 'QMS,' 'ISO 13485,' 'risk mitigation,' and 'validation documents' to improve your chances of passing initial screenings.
Use Jennie Johnson's Power Apply feature to automate the tailored application submissions, find relevant job postings across multiple sites, and identify LinkedIn contacts for networking, allowing you to focus your energy on preparing for interviews and skill development.
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