BioTechne

Manager, Program Management

BioTechne • $115K — $189K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree or Ph.D. in scientific or related field; strong background in spatial genomics and in-vitro diagnostics
  • Preferred PMP, PgMP, or equivalent project/program management certification
  • Over 5 years of project management experience in complex, cross-functional settings
  • Experience managing multiple projects or portfolios while establishing governance
  • Background in life sciences, biotechnology, diagnostics, or medical device product development is preferred
  • Knowledge of quality and regulatory practices with experience in regulated products is a plus
  • Advanced skills in project planning, risk management, and stakeholder communication.

Responsibilities

  • Lead RNAscope project portfolio with integrated view of priorities and risks
  • Oversee program management for RNAscope initiatives, ensuring alignment with business objectives
  • Facilitate prioritization discussions and escalate issues requiring leadership attention
  • Provide concise portfolio reporting to SBD leadership regarding progress and constraints
  • Ensure consistent application of PMO standards and governance practices in Newark
  • Contribute to annual strategic planning and project prioritization activities
  • Lead cross-functional teams through the product commercialization process from concept to launch

Benefits

  • Comprehensive health insurance including medical and dental coverage
  • Retirement savings plan with company matching contributions
  • Opportunities for professional development and continuous learning
  • Flexible work hours and potential for hybrid work environment
Full Job Description

Pay Range:

$115,100.00 - $189,200.00

Job Purpose

The Manager, Program Management leads the RNAscope project portfolio and the Newark-based Project Management Office (PMO) within the Spatial Biology Division (SBD). Reporting to the Director, PMO, who is accountable for the overall SBD PMO, this position provides local people leadership and portfolio oversight, while ensuring alignment with SBD-wide PMO governance, standards, priorities and reporting expectations.

The role enables effective prioritization, execution and decision-making across new product introductions (NPI), sustaining, operational, process improvement and strategic initiatives. It partners closely with Product Management, R&D, Operations, Quality Assurance, Commercial, and other cross-functional leaders to deliver business priorities in alignment with company quality policies and established product commercialization processes. This role is also expected to directly manage multiple NPI and sustaining projects, process improvement initiatives and supervise a small team of project managers.

Responsibilities

Portfolio and Program leadership:

  • Lead the RNAscope project portfolio and maintain an integrated view of priorities, milestones, dependencies, resources, risks, and expected business outcomes.
  • Provide program and project management oversight for RNAscope initiatives, including RUO, OEM and IVD NPI projects, as well as sustaining, operational, process improvement and strategic initiatives, as applicable.
  • Facilitate portfolio prioritization, capacity discussions, and risk-based decision-making; escalate issues and trade-offs when leadership action is required.
  • Provide concise, decision-oriented portfolio reporting to SBD leadership, including progress, risks, dependencies, resource constraints, and recommended actions.
  • Ensure consistent application of SBD PMO project and program management standards, tools, templates, and governance practices within the Newark PMO.
  • Provide input for annual strategic planning and prioritization activities.

Project execution:

  • Lead cross-functional core teams through established product commercialization and stage-gate processes from concept through launch and post-launch follow-up.
  • Develop and maintain clear project plans, milestones, decision points, resource needs, stakeholder communications and risk mitigation actions.
  • Partner with cross-functional stakeholders to continuously improve relevant project management and product commercialization processes.

Team supervision:

  • Lead and develop a small team of Project Managers in the Newark PMO team through goal setting, coaching, workload allocation, performance support, and professional development.
  • Build strong alignment between Newark and other SBD locations to support effective communication, handoffs and execution of shared priorities.

Qualifications

Education:

  • Master27s degree or Ph.D. in scientific or related field with good understanding of spatial genomics technologies and in-vitro diagnostics concepts.
  • PMP, PgMP, or an equivalent project/program management certification is preferred.

Skills and Experience:

  • At least 5 years of demonstrated project management experience, including responsibility for complex, cross-functional initiatives.
  • Experience managing multiple projects or a portfolio, establishing governance, balancing competing priorities, and driving decisions with incomplete or evolving information.
  • Experience in life sciences, biotechnology, diagnostics, or medical device product development is strongly preferred.
  • Working knowledge of standard quality and regulatory practices; experience with regulated products (e.g. GPR, ASR, IVDR) is highly desirable.
  • Advanced project planning, risk management, facilitation, stakeholder management, and executive communication skills.
  • Working knowledge of project management tools.
  • Excellent interpersonal and influencing skills, with the ability to work effectively across functions, sites, and leadership levels.
  • Highly organized, accountable, and comfortable operating independently in a dynamic and ambiguous environment.

About BioTechne

Bio-Techne Corporation develops, manufactures, and sells life sciences tools, diagnostics, and reagents worldwide. The company operates in three segments: Protein Sciences, Diagnostics and Genomics, and Clinical Controls. The Protein Sciences segment offers proteins and reagent solutions, including cytokines and growth factors, antibodies, immunoassays, biologically active small molecule compounds, tissue culture reagents, and T-Cell activation technologies. The Diagnostics and Genomics segment provides blood chemistry and blood gas quality controls, hematology instrument controls, diagnostic immunoassays, and other bulk and custom reagents for the in vitro diagnostic market. The Clinical Controls segment offers a range of products comprising Thrombin Generation Assays, and quality controls and calibrators for various clinical instruments. The company was founded in 1976 and is headquartered in Minneapolis, Minnesota.
Learn more about BioTechne
Size
2,600 employees
Market Cap
$12.9 billion
Industry
Net Income
$174.9 million
Founded
1981
5 Year Trend
+14.5%
Revenue
$798.9 million
NASDAQ

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