Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
AtBeckman Coulter Diagnostics, one ofDanahers15+ operating companies, our work saves livesand were all united by a shared commitment to innovate for tangible impact.
Youll thrive in a culture of belonging where you and your unique viewpoint matter. Andby harnessingDanahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life.
As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratorys role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision makingwe are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.
TheSr.Manager,Global ProcessEngineeringis responsible forleading andshaping our manufacturing capabilities and ensuring the highest standards of quality and efficiency in medical device production. You will lead a team of talented engineers, overseeing the development, optimization, and validation of manufacturing processes from concept to commercialization. This role requires a strategic thinker with deep technical expertise, exceptional leadership skills, and a strong commitment to regulatory compliance within the medical device industry.
This position reports to the VP, Global Engineering, and is part of the Global Engineering team. This will be a remoteposition, preferably near Chaska,Minnesotaornearan airport for travel.
Strategic Leadership & Management: Lead, mentor, and develop a highperforming Process Engineering team, fostering a culture of continuous improvement, accountability, and technical excellence.
Process Development:Define and execute process engineering strategies aligned with business objectives, including production efficiency, cost reduction, quality improvement, and new product introduction (NPI).
Validation:Oversee the design, development, and optimization of scalable, costeffective manufacturing processes for new and existing medical device products using Lean and Six Sigma methodologies.
Optimization:Oversee the design, development, and optimization of scalable, costeffective manufacturing processes for new and existing medical device products using Lean and Six Sigma methodologies.
Financial Acumen:Manage departmental budgets, resources, and project prioritization to ensure effective execution of strategic and operational goals.
Compliance:Ensure full compliance with FDA 21 CFR Part 820, ISO 13485, and global regulatory requirements, including ownership of process validation (IQ/OQ/PQ), documentation, and audit support
Cross-functional Collaboration:Collaborate crossfunctionally with R&D, Quality, Operations, Supply Chain, and Regulatory teams to support technology adoption, equipment implementation, and successful product transfers.
The essential requirements of the job include:
Education:Bachelors degree in Engineering(Biomedical, Mechanical, Electrical, Industrial, Manufacturing) or a closely related technical field;Mastersdegree or MBA preferred.
Experience:10+ years of experience in Process Engineering within a regulated medical device manufacturing environment.
Leadership Experience:5+ years of people leadership experience, including managing, developing, and mentoring engineering teams.
Technical Skills:Demonstrated expertise in FDA 21 CFR Part 820, ISO 13485, and applicable global medical device regulatory requirements.
Methodologies:Proven success leading process improvement initiatives, supported by Lean Six Sigma methodologies and certifications (Green or Black Belt preferred).
Technical Skills:Strong technical background in process validation (IQ/OQ/PQ), statistical process control (SPC), and datadriven manufacturingdecisionmaking.
Industry Knowledge:Experience across complex manufacturing processes (e.g., injection molding, assembly, sterilization, packaging, automation, and/or cleanroom operations), withstrong communication, project management, and cross-functional collaboration skills.
Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
Ability to travel60-70%travelif remote work arrangement,40-50% if on-site/hybrid
Must have a valid drivers license with an acceptable driving record
Beckman Coulter Diagnostics,a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether its a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits atDanaher Benefits Info.
AtBeckman Coulter Diagnosticswe 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 forBeckman Coulter Diagnosticscan provide.
The annual salaryrange forthis role is$160k-$190k. 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 payis considered to bewages 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 Companys sole discretion, consistent with the law.
Join our winning team today. Together, well accelerate the real-life impact of tomorrows 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.
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 comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.
