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 Manufacturing Engineer for Cytiva is responsible with resolving daily operational challenges and engaging in strategic initiatives focused on new product development and ongoing improvements in the manufacturing of bioprocessing hardware. By building expertise, you will become a Subject Matter Expert (SME), responsible for modifying, optimizing, and monitoring manufacturing processes to lower defect rates and boost productivity. This position is part of the Hardware Manufacturing Engineering team located in in Shrewsbury, MA and will be on-site position. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: + Process Enhancement: Demonstrates a solid understanding of existing processes to support in the development and improvements to the manufacturing process with a focus on upstream bioprocessing hardware products. + Technical Expertise: Serves as the primary point of technical escalation, proficient in troubleshooting, developing manufacturing tooling/fixtures, and resolving operational issues. + Productivity Improvements: Monitors and enhances productivity using DBS fundamental tools, ensuring timely and cost-effective fulfillment to meet customer commitments, while also focusing on manufacturability and safety considerations. + Product Quality: Drive continuous improvements in product quality by identifying manufacturing issues, devising cost-effective solutions, and overseeing their successful implementation in production. + Quality and Regulatory Compliance: Supports the alignment of manufacturing processes with company objectives, industry best practices, and regulatory requirements, ensuring adherence to both external and internal quality standards and protocols. Who you are: + A Bachelor's degree in Mechanical, Electrical, or Manufacturing, or Computer Systems Engineering (or a related technical field), or an Associate's degree with multiple years of experience in engineering, or production/troubleshooting of bioprocessing equipment. + Demonstrated capability to solve problems, using troubleshooting, analytical, and planning skills. + Working knowledge of lean manufacturing principles using quality improvement techniques. + Demonstrated communication skills (written and verbal) with all levels of the organization. It would be a plus if you also possess previous experience in: + Experience with Computer-Aided Design (CAD), Embedded Systems, Coding/Macros and Mechanical Design is preferred. + Experience working in the Bio-Science, Medical Device, or Pharma industries is preferred. The base salary range for this role is $70k—$85k. 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. We may ultimately pay more or less than the posted range, and this range may be modified in the future.This job is also eligible for bonus/incentive pay. We offer a comprehensive package of benefits, including paid time off, health insurance, and retirement planning benefits, to eligible employees.Note: No pay amount is considered wages or compensation until it is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits allocable to a particular employee remain 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 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.