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Bio-Techne

Senior Project Manager

Bio-Techne

. Lead multiple complex New Product Introduction (NPI), sustaining engineering, and strategic initiatives across the ASD portfolio, primarily Simple Western and Biologics .

Posted 11/5/2026full-timeUnited StatesSenior💰 $91,700 - $150,800 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading New Product Introduction (NPI) initiatives and managing cross-functional teams in the life sciences sector. Proficient in project management, risk mitigation, and utilizing data analytics tools for effective decision-making and communication.

Highest-signal resume keywords
New Product Introduction (NPI) ManagementCross-Functional Team LeadershipProject Management in Life SciencesRegulatory Compliance ExperienceData Analytics and Visualization

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project ManagementRisk ManagementTechnical Project ManagementProduct Lifecycle ManagementMicrofluidicsAssay DevelopmentVerification and ValidationManufacturing TransferDesign ReviewsAnalytical Instrumentation
Soft Skills
Influencing Without AuthorityProblem-SolvingExecutive CommunicationFacilitation SkillsCollaboration
Tools & Technologies
Power BIJiraSmartsheetData Analytics ToolsAI-Enabled Tools
Certifications & Qualifications
ISO 9001ISO 13485GMP Certification
Industry Keywords
Life SciencesBiotechnologyMedical DevicesAnalytical InstrumentationQuality Environment

About the role

Key responsibilities & impact
  • Lead multiple complex New Product Introduction (NPI), sustaining engineering, and strategic initiatives across the ASD portfolio, primarily Simple Western and Biologics
  • Drive cross-functional teams through product development, verification, validation, manufacturing transfer, launch, and post-launch activities
  • Develop integrated project plans, critical paths, resource forecasts, and dependency management across hardware, software, consumable, reagent, and manufacturing workstreams
  • Identify, communicate, and mitigate technical, schedule, supply chain, quality, and commercialization risks
  • Facilitate phase-gate reviews, design reviews, executive reviews, and portfolio governance activities
  • Partner with Engineering, Product Management, Supply Chain, Manufacturing, Quality, Regulatory, and Commercial teams to achieve project objectives
  • Provide concise executive-level communication on project status, risks, mitigation plans, and decisions required
  • Use data analytics and AI-enabled tools to improve execution, forecasting, reporting, and portfolio visibility
  • Develop portfolio dashboards and metrics using Power BI, Jira, Smartsheet, or other platforms
  • Drive resolution of complex technical and organizational challenges through influence and cross-functional collaboration
  • Coach project managers and contribute to continuous improvement of PMO processes, tools, and best practices

Requirements

What you’ll need
  • Bachelor's degree in mechanical engineering, Biomedical Engineering, Chemical Engineering, Systems Engineering, Life Sciences, or related discipline
  • 8+ years of technical project or program management experience in life sciences, biotechnology, medical devices, analytical instrumentation, or a related industry
  • Demonstrated experience managing multiple concurrent NPI programs and leading cross-functional teams through the full product lifecycle
  • Experience collaborating with mechanical, electrical, software, systems, manufacturing, quality, regulatory, and supply chain functions
  • Experience presenting project status, risks, trade-offs, and recommendations to senior and executive leadership
  • Experience working in a regulated quality environment, such as ISO 9001, ISO 13485, GMP, or comparable product development controls
  • Experience leading life science instrument or analytical instrument launches
  • Experience with microfluidics, fluidics, cartridges, consumables, capillary electrophoresis, protein characterization, assay development, or hardware-intensive products
  • Experience with design reviews, systems engineering, verification and validation, manufacturing transfer, pilot builds, and production scale-up
  • Strong technical aptitude and ability to engage engineering teams in detailed product-development discussions
  • Exceptional critical-path, dependency, risk, resource, and stakeholder management skills
  • Ability to influence cross-functional teams and senior stakeholders without direct authority
  • Strong analytical, problem-solving, and data-visualization capabilities
  • Ability to translate complex technical information into clear business recommendations and decisions
  • Excellent written, verbal, facilitation, and executive presentation skills
  • Demonstrated success leading through ambiguity, competing priorities, and resource constraints in a fast-paced environment
  • Ability to work independently while maintaining strong alignment across distributed teams and sites
  • Must have work authorization that does not now or in the future require visa sponsorship in the United States

Benefits

Comp & perks
  • Medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield insurance benefits starting on day one
  • 401k plans
  • Employee stock purchase plan (ESPP)
  • Health Saving Account (HSA)
  • Flexible Spending Account (FSA)
  • Dependent Care FSA
  • Mentorship
  • Promotional opportunities
  • Training and development
  • Tuition reimbursement
  • Internship programs
  • Employee resource groups
  • Volunteer paid time off
  • Employee events
  • Charity drives
  • Paid holidays
  • Paid time off
  • Paid parental leave
  • Culture of empowerment and innovation