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Project Manager Biotech Jobs in Minnesota (NOW HIRING)

Barrington James

Project Manager

Maple Grove, MN · On-site

Project Manager II - Pharmaceutical CDMO (Oral Solid Dose / Biologics / Sterile Injectables) Our ... PMP certification preferred * 6+ years of cGMP experience in oral solid dose (preferred), biotech ...

PSC Biotech

Cleaning Validation Engineer

Minneapolis, MN · On-site

$90K - $105K/yr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Develop, modify, execute, and manage cleaning validation protocols for harvest centrifuges ...

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How much do project manager biotech jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for project manager biotech in Minnesota is $45.29, according to ZipRecruiter salary data. Most workers in this role earn between $39.33 and $49.66 per hour, depending on experience, location, and employer.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What are popular job titles related to Project Manager Biotech jobs in Minnesota?

For Project Manager Biotech jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Project Manager Biotech jobs in Minnesota look for?

The top searched job categories for Project Manager Biotech jobs in Minnesota are:

What cities in Minnesota are hiring for Project Manager Biotech jobs?

Cities in Minnesota with the most Project Manager Biotech job openings:

Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Minnesota as of August 2026, with employment types broken down into 100% Full Time. Highlights an 71% In-person, and 29% Hybrid job distribution, with an average salary of $94,204 per year, or $45.3 per hour.

Project Manager

Maple Grove, MN • On-site

Barrington James
See more jobs at Barrington Jamesexternal

Other

Posted 6 days ago

Job description

Project Manager II – Pharmaceutical CDMO (Oral Solid Dose / Biologics / Sterile Injectables)


Our client is a fast-growing international CDMO providing formulation development, clinical and commercial manufacturing, and packaging services across oral solid dose, liquid, semi-solid, biologics, and sterile injectable products. With manufacturing sites across North America and Asia, they support clients delivering therapies to more than 100 global markets.


The Role

We're seeking a Project Manager II to lead cross-functional project management across development, technical transfer, and operational workstreams supporting the full product lifecycle at a US manufacturing site — including purchase orders, forecasting, change orders, invoicing, and shipping coordination. This person will own the client engagement model, driving consistent, proactive communication and relationship management with both internal teams and external clients. They'll be accountable for keeping project milestones and budgets on track, including full visibility on pass-through and change order costs.

This is a highly visible role central to the site's growth in development and technical transfer work, requiring someone who can translate technical, financial, and commercial considerations into smooth project execution.

Expect to be on-site 3–4 days per week, with flexibility to prioritize client visits as needed.


What You'll Do

  • Support timelines during the quotation process and partner early with Business Development to ensure a seamless handoff once contracts are signed
  • Coordinate client visits, including due diligence and person-in-plant activities
  • Own financial forecasting and invoicing accuracy, building contingency plans when things fall off track
  • Manage and forecast project budgets, ensuring change orders are processed in a timely manner
  • Lead internal and external client meetings, providing fast, consistent feedback to all stakeholders
  • Manage routine client communications — messaging, escalations, and notifications
  • Escalate client issues appropriately across the management team, relevant functions, and site/BU leadership
  • Act as a site operations business manager alongside Supply Chain leadership to:
  • Align client support with production priorities and forecasts
  • Manage client inventory positions and communicate market strategy needs
  • Support the Ambassador team in delivering top-tier client service and escalation handling
  • Ensure information flows smoothly across site functions and the broader CDMO business unit
  • Facilitate handoff of client products from NPI/qualification into steady-state portfolio management
  • Drive continuous improvement, deviation investigations, and CAPA efforts for assigned clients
  • Build and maintain effective tools, templates, and meeting cadences to support client engagement
  • Partner with EH&S to ensure safe, compliant execution of on-site client activities


What We're Looking For

  • Bachelor's degree in Project Management, Business, or a related pharmaceutical sciences discipline; PMP certification preferred
  • 6+ years of cGMP experience in oral solid dose (preferred), biotech, or bio-pharmaceutical manufacturing — ideally spanning pre-clinical through commercial phases — or equivalent experience in commercial operations/client portfolio management
  • Strong grasp of financial fundamentals: invoicing, forecasting, and budget impact within pharma/biopharma manufacturing
  • 6+ years managing critical relationships between suppliers/providers and clients
  • FDA experience, including regulatory inspection participation, a plus
  • Excellent cross-functional collaboration skills, both internally and across a multi-client portfolio
  • Confident, clear communicator — written and verbal — comfortable driving conversations
  • Self-directed, with sound judgment on compliance matters and a proactive approach to risk mitigation
  • Track record of ownership and delivery-focused execution


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