Lead Development Engineer

Cytiva; Marlborough (MA); In loco; USD 87.000 - 100.000; Tempo pieno

Descrizione del lavoro

Cytiva in Marlborough, MA is seeking a Lead Development Engineer to guide mechanical design from concept to release for bioprocessing equipment. Working on a cross-functional R&D team, you will develop safe, manufacturable, cost‑effective products and mentor engineers.

You will create drawings, manage BOMs, and define design inputs while ensuring GDP traceability and regulatory readiness. On-site role with opportunities to influence lifecycle improvements and collaborate with suppliers and

Competenze

• BS in Mechanical Engineering or related field; master's degree is a plus.
• 3+ years of product development experience in bioprocessing, life sciences, medical devices, or regulated products.
• Experience with Creo, PLM/PDM, FEA; knowledge of GD&T and tolerance analysis.
• Hands-on engineering with prototype fabrication and testing (metal/plastic), welding, additive manufacturing.
• Ability to mentor engineers and collaborate across functions; work with suppliers and manufacturing partners.

Mansioni

• Lead design, development, and refinement of mechanical components, assemblies, and systems to meet performance, cost, reliability, and manufacturability goals.
• Create and review engineering drawings, specifications, 3D models, and other design outputs using CAD tools and standard design practices.
• Maintain bills of materials (BOMs) in MRP/ERP systems and lead engineering change request (ECR) and engineering change order (ECO) activities.
• Define and document design inputs while maintaining traceability between requirements, design outputs, risk management, and verification activities per GDP.
• Lead technical activities for assigned projects by mentoring junior engineers, facilitating design reviews, resolving technical challenges, and promoting engineering best practices.

Conoscenze

Mechanical design

Prototyping

GD&T

Creo

FMEA

Formazione

BS in Mechanical Engineering

MS is a plus

Strumenti

Creo

PLM/PDM

FEA

Descrizione del lavoro

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

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 Danaher’s 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 Danaher Business System which makes everything possible.

The Lead Development Engineer will lead product development activities from concept through commercial release, including new product introductions, sustaining engineering, and line extensions for bioprocessing equipment. As part of the R&D team, this role independently develops technical solutions, leads engineering workstreams, and collaborates across functions to deliver safe, reliable, manufacturable, and cost‑effective products.

This position reports to the Principal Hardware Engineer and is part of the R&D team based in Marlborough, MA, with occasional work in Shrewsbury, MA. This is an on‑site role.

What You Will Do

• Lead the design, development, and refinement of mechanical components, assemblies, and systems to meet performance, cost, reliability, and manufacturability goals.
• Create and review engineering drawings, specifications, 3D models, and other design outputs using CAD tools and standard design practices.
• Maintain bills of materials (BOMs) in MRP/ERP systems and lead engineering change request (ECR) and engineering change order (ECO) activities.
• Define and document design inputs while maintaining traceability between requirements, design outputs, risk management, and verification activities throughout product development in accordance with Good Documentation Practices (GDP).
• Lead technical activities for assigned projects by mentoring junior engineers, facilitating design reviews, resolving technical challenges, and promoting engineering best practices.

Who You Are

• You have a BS in Mechanical Engineering or a related field; a master’s degree is a plus.
• You have 3 or more years of product development experience. Experience with bioprocessing equipment, life sciences, medical devices, industrial equipment, or other regulated products is preferred.
• You are proficient in engineering documentation, product development processes, and mechanical design principles, including GD&T and tolerance stack‑up analysis. Experience with Creo, PLM/PDM systems, FEA, and applicable product safety and regulatory standards is a plus.
• You enjoy hands‑on engineering work and have experience with prototype fabrication and testing, including metal and plastic fabrication, drilling, cutting, assembly techniques, fastener selection, welding methods, additive manufacturing (3D printing), troubleshooting, and evaluation of hardware designs.
• You can independently execute engineering projects, perform technical analysis and problem solving, contribute to risk management and root‑cause investigations, mentor junior engineers, collaborate effectively across functions, and work with suppliers and external manufacturing partners to support product development and lifecycle improvements.

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 Danaher Benefits Info.

The annual salary range for this role is $87,000 to $100,000. 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.

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.

The U.S. EEO posters are available here.

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 [e-mail].