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Manufacturing Project Leader – Life Sciences, Bioreactors, NPI, Mfg. Transfer
Danaher Corporation. Manage projects to introduce new products into Cytiva operational business units .
Posted 11/9/2026full-timeWestborough • Massachusetts • United StatesSenior💰 $92,500 - $120,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Project Management and New Product Introduction within regulated environments, ensuring compliance and process standardization while driving improvements in product quality and productivity. Proficient in risk management and validation processes, with a strong background in manufacturing technologies and lean methodologies.
Highest-signal resume keywords
Project ManagementNew Product IntroductionRegulatory ComplianceLean ManufacturingRisk Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project PlanningProduct Life Cycle ManagementValidation and VerificationRoot Cause AnalysisSix SigmaStatistical ToolsEquipment Automation TheoryDesign for ManufacturingInnovation DevelopmentTesting and Qualification
Certifications & Qualifications
Bachelor’s Degree in Mechanical EngineeringBachelor’s Degree in Electrical EngineeringBachelor’s Degree in Industrial Engineering
Industry Keywords
Medical Device IndustryManufacturingSingle Use TechnologiesConsumablesHardware Products
About the role
Key responsibilities & impact- Manage projects to introduce new products into Cytiva operational business units
- Oversee global projects for multi-site standardization, process improvements, transfers of work and feature product additions
- Ensure successful new product development launches and process standardization into manufacturing
- Drive rigor on supply chain aspects including Product Life Cycle Management
- Manage risks and mitigation planning through creative solutions
- Represent manufacturing on global cross-functional business project teams and process development teams
- Ensure regulatory compliance through validation and verification
- Determine processes requiring validation, develop plans and analysis criteria, and execute final analysis and acceptance
- Work with business area leaders and manufacturing engineers to improve product quality and productivity
- Identify manufacturing issues, develop cost-effective solutions, and oversee implementation into production
Requirements
What you’ll need- Bachelor’s degree in mechanical engineering, Electrical Engineering, Industrial Engineering or related technical field
- Prefer minimum of 8 years of experience in production or engineering, regulated / medical device or related industry experience
- Prefer minimum of 5 years of experience with Project Planning and Project Management and managing multiple projects to successful completion
- Prefer minimum of 5 years of experience of Innovation, Development, Testing and Qualification as relates to New Product Introduction
- Ability to travel – 15% travel globally
- Must have a valid driver’s license with an acceptable driving record
- Ability to lift, move or carry equipment up to 35lb
- Equipment automation theory and design experience is a plus
- Manufacturing of single use technologies for consumables and hardware products (Mixers and Bioreactor) experience is a plus
- Lean manufacturing, design for manufacturing, 5S, 3P, root cause analysis, six sigma and statistical tools & analysis experience is a plus
Benefits
Comp & perks- Bonus/incentive pay
- Paid time off
- Medical insurance
- Dental insurance
- Vision insurance
- 401(k)