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Life Science Project Manager Jobs in Wisconsin (NOW HIRING)

WI · On-site

$92K - $120K/yr

We are looking for aProject Manager with BMS (Honeywell) expertise to lead building automation and environmental monitoring projects within a GxP regulated Life Sciences environment in Belgium.In ...

Our services help improve the quality of life in the communities where we live and work. We always ... As a Senior Project Manager for our Industrial Hygiene/Building Science team, you'll support ...

WI · On-site

YOUR ROLE As a Senior Project Manager, you are accountable for delivering complex, high-impact ... Experience in the life science sector is a strong advantage. WHAT YOU'LL LOVE ABOUT WORKING HERE?

WI · On-site

Operations Supervisor - Life Science Division Full-time Management Easton, Easton, PA, US 23 days ago Requisition ID: 1386 This is a 1st shift position: Tuesday - Saturday, 8A - 4P The Operations ...

... the Life Sciences, Mission Critical, Metals, Material Handling, Consumer Products and Food ... We are seeking a Project Manager to lead a large project or multiple project efforts, which may ...

... the Life Sciences, Mission Critical, Metals, Material Handling, Consumer Products and Food ... We are seeking a Project Manager to lead a large project or multiple project efforts, which may ...

... the Life Sciences, Mission Critical, Metals, Material Handling, Consumer Products and Food ... We are seeking a Project Manager to lead a large project or multiple project efforts, which may ...

By combining top talent from the life sciences industry with modern research and manufacturing ... Position Project Manager Location Philadelphia, PA Summary The Project Manager is primarily ...

WI · On-site

$95K - $135K/yr

... Life Sciences, and Mission Critical markets. Guided by The Thermo Way , we are unified, dynamic ... The Opportunity The Project Manager is accountable for the successful delivery of customer projects ...

New

... Life Science, Insurance, legal, healthcare, among others. It also offers outsourcing, consulting ... SAP Finance Project Manager Racine, WI Start date ASAP 6 months - but could go 15 months or longer ...

CMC Project Manager ICON is a global healthcare intelligence and clinical research organisation ... Life Sciences degree * strong CMC project experience. * Experience in working with biologics

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Life Science Project Manager information

What is a life science project manager?

Life Science Project Managers are professionals responsible for planning, coordinating, and overseeing projects within the life sciences sector, such as pharmaceuticals, biotechnology, medical devices, or healthcare research. They ensure projects are completed on time, within budget, and in compliance with regulatory requirements. Their role involves managing cross-functional teams, facilitating communication between stakeholders, and identifying potential risks to project timelines or goals. Life Science Project Managers play a crucial role in bringing scientific innovations to market efficiently and safely.

What are the key skills and qualifications needed to thrive as a life science project manager?

To thrive as a Life Science Project Manager, you need a solid background in life sciences or a related field, project management experience, and often a relevant degree or certification like PMP. Familiarity with project management software (such as MS Project or Asana), regulatory systems (GxP, FDA, EMA), and data analysis tools is typically required. Strong leadership, communication, and problem-solving abilities help you coordinate cross-functional teams and manage complex project timelines. These skills are critical to ensure projects are completed efficiently, within regulatory compliance, and deliver successful results in the fast-evolving life sciences industry.

What are some common challenges faced by life science project managers, and how can they be addressed?

Life Science Project Managers often encounter challenges such as coordinating cross-functional teams, managing strict regulatory requirements, and adapting to evolving project scopes. Balancing timelines and budgets while ensuring compliance with industry standards can be demanding. Successful project managers address these challenges by fostering clear communication, implementing robust project management tools, and staying informed on regulatory changes. Building strong relationships with stakeholders and proactively identifying risks also contribute to smoother project execution.

What is the difference between Life Science Project Manager vs Research Scientist?

AspectLife Science Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Life Sciences, PMP certification often preferredAdvanced degree (Master's or PhD) in relevant scientific field
Work EnvironmentProject teams, labs, corporate settingsResearch labs, academic institutions, industry R&D
Employer & Industry UsageBiotech, pharma, healthcare companiesResearch institutions, universities, biotech firms
Common Search & ComparisonOften compared for project management roles in life sciencesCompared for scientific research roles

The main difference is that a Life Science Project Manager oversees projects, timelines, and teams within life sciences companies, focusing on coordination and delivery. In contrast, a Research Scientist conducts experiments and generates scientific data. Both roles require relevant credentials, but the Project Manager emphasizes management skills, while the Research Scientist emphasizes scientific expertise.

What cities in Wisconsin are hiring for Life Science Project Manager jobs?

Cities in Wisconsin with the most Life Science Project Manager job openings:

Infographic showing various Life Science Project Manager job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

CDMO Project Manager

Beloit, WI

NorthStar Medical Radioisotopes
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Key responsibilities

  • Manage the end-to-end project lifecycle of CDMO projects, including kickoff, technology transfer, validation, and manufacturing.

  • Serve as the main liaison between sponsors, internal teams, and external partners to manage expectations and communicate project updates.

  • Develop and track project plans, schedules, and deliverables, and coordinate resources to ensure project goals are met.


Job description

Join the best radiopharmaceutical company in the world!

If you’re looking to make an impact while building a meaningful career in a specialized, fast-growing field, NorthStar Medical Radioisotopes is the place to do it. NorthStar Medical Radioisotopes is a growing, commercial-stage company focused on advancing patient care by providing therapeutic radioisotopes and novel radiopharmaceuticals to detect and treat cancer.

At the forefront of NorthStar’s technological innovation is scientific excellence, using first-in-kind electron accelerator technology and integrated campus capabilities to drive progress in radiopharmaceutical manufacturing. Our work is driven by a meaningful mission—advancing life-saving radiopharmaceutical development and ensuring a reliable supply of critical medical isotopes for patients in need. As a rapidly growing organization operating on the cutting edge of science, we offer exceptional career growth and professional development opportunities, supported by world-class facilities and a competitive benefits package.


This position will shepherd Contract Development and Manufacturing Organization (CDMO) projects through their life cycle at NorthStar, including initial kickoff, technology transfer, validation, and drug product manufacturing, both clinical and commercial. The CDMO Project Manager is responsible for providing internal and external leadership for CDMO projects. This role will serve as the main contact for driving the tactical execution of CDMO projects upon contract approvals. This role may also provide support to the Commercial organization in the outreach and courting of new sponsors.


  • Lead the end-to-end project management of CDMO projects from kickoff through technology transfer, validation, and manufacturing (clinical and commercial phases).
  • Act as the main liaison between sponsors, internal teams, and external partners to manage expectations, provide updates, and escalate issues when necessary.
  • Develop, manage, and track comprehensive project plans, charters, schedules, and deliverables, ensuring alignment with business goals and sponsor expectations.
  • Support Operations management, Business Development and Finance to achieve project revenue targets and summarize project-level financial performance.
  • Collaborate with facility management and other functions to determine resource requirements for each project, including personnel, equipment, and materials.
  • Organize project dashboards and project performance reports for management, communicating delays/problems and providing mitigation plans and recommendations, as necessary.
  • Develop a high-level understanding of all aspects of the project to serve as a liaison for questions and comments regarding project status.
  • Work closely with internal and external stakeholders to clearly define project goals, both short-term and long-term, for broader dissemination.

  • Continuously seek opportunities to optimize project execution, improve efficiency, and enhance customer satisfaction.

After 3 months, you will:

  • Develop a strong understanding of NorthStar's CDMO business, project lifecycle, sponsor expectations, and cGMP environment while building relationships with key internal and external stakeholders. 
  • Support project planning and execution activities, including maintaining project schedules, tracking action items, preparing status updates, coordinating meetings, and managing project documentation. 
  • Gain proficiency in NorthStar's project management processes and begin contributing to project risk identification, resource planning, and cross-functional coordination efforts.

After 6 months, you will: 

  • Independently manage assigned CDMO projects, serving as the primary liaison between sponsors and internal teams while ensuring alignment with project objectives, timelines, and customer expectations.
  • Lead project meetings, maintain project plans and dashboards, proactively identify and mitigate risks, and drive accountability for project deliverables and milestones. 
  • Coordinate technology transfer and project readiness activities, provide leadership across cross-functional teams, and contribute to continuous improvement initiatives that enhance project execution and customer satisfaction.

Bachelor’s degree in technical discipline and minimum six (6) years of project management experience in the life science industry, inclusive of a minimum of two (2) years of cGMP experience, and at least five (5) years of experience in a technical role in life science operations including some technology transfer experience; or equivalent combination of education and experience. Knowledge of cGMP working environment would be beneficial. PMP Certification highly desirable.

Please note the company cannot provide immigration-related sponsorship (including H-1B status, O-1 status, Optional Practical Training support, etc.) for this position.  Each successful applicant will be required to complete the Form I-9, Employment Eligibility Verification, demonstrating both identity and employment authorization, on or before the first day of employment.  Under federal law, only truthful information may be provided on the Form I-9.



  • Medical, dental, and vision insurance
  • Healthcare Flex Spending Account (FSA) and Dependent Care FSA
  • Company-paid short-term and long-term disability
  • Company-paid life insurance & AD&D coverage
  • Pet insurance
  • 401(k) match
  • Paid holidays and paid time off (PTO)
  • Paid parental leave
  • Bonus plan
  • Equity Incentive Program

This role may involve working in a controlled cleanroom environment, general office setting, or specific manufacturing areas. Conditions may include:

  • Exposure to varying temperatures, both indoors (heated/air-conditioned spaces) and outdoors
  • Noise levels range from quiet to loud, depending on the work area
  • Specific vision abilities, including near vision, visual acuity, and color discrimination

Personal Protective Equipment (PPE) is required and may include:

  • Respirators, gloves, safety glasses, and full protective clothing
  • Compliance with cleanroom gowning protocols (e.g., removal of all jewelry, including piercings)
  • Prohibition of cosmetics, fragrances (perfume, aftershave), and nail products, including polish, artificial nails, or extensions

As a radiopharmaceutical manufacturing site, radiation may be present in the laboratory and production areas. Employees in this role may be required to:

  • Follow strict radiation safety procedures
  • Participate in dosimetry monitoring and bioassay testing as part of the company protocol
  • Inform leadership of any health conditions that may affect product integrity, by cleanroom standards

NorthStar Medical Radioisotopes is proud to call Beloit, Wisconsin home. Our headquarters and primary manufacturing facility are located in this vibrant, growing community that combines the charm of a small city with the advantages of a central Midwest location. Beloit features a lively, revitalized downtown filled with local restaurants, shops, and cultural events, and is just a short drive from major metropolitan areas including Madison, Milwaukee, Chicago, and Rockford.

Situated in the heart of the South Central Wisconsin and Northern Illinois region, Beloit offers a rare blend of urban amenities and scenic natural surroundings. Whether you’re drawn to outdoor recreation, educational institutions, the arts, or historic landmarks, the area provides rich and diverse experiences for all interests. A variety of nearby communities, ranging from rural towns to suburban neighborhoods, offer flexible housing options and access to multiple school districts, making Beloit an excellent choice for individuals and families considering relocation.

Please note that this position is eligible for a lump sum relocation benefit!

NorthStar Medical Radioisotopes is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.