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Pharma Project Manager Jobs in Minnesota (NOW HIRING)

Pwc

Rewards- Benefits Rx- Senior Manager

Minneapolis, MN

$124K - $280K/yr

As a Senior Manager, you will leverage your skills and professional network to deliver quality ... projects in the pharma and life sciences sector - Applying systems thinking to identify and solve ...

Bilfinger

Lead Electrical Engineer

Groningen, MN · On-site

$156K - $163K/yr

... pharma en complexe gebouwen. Als jij de ambitie hebt, hebben wij een carrière voor jou bij een ... Samen met de projectmanager en de lead engineers van de andere disciplines coördineer je het ...

Artius Solutions

Business Analyst

Minneapolis, MN · On-site

$60 - $65/hr

... project. The role involves gathering business requirements, working with stakeholders, and ... Good communication and stakeholder management Preferred: * Experience in Life Sciences or Pharma

GEA

Regional Sales Manager - Dairy

Cottage Grove, MN · On-site

$100K - $150K/yr

... and beverage, pharma, dairy, and more. With over 18,000 employees worldwide and a strong U.S ... Acquire sales and market intelligence on issues such as competition, price, and project status

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Pharma Project Manager information

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How much do pharma project manager jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for pharma project manager 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 Pharma Project Manager do?

A Pharma Project Manager oversees and coordinates pharmaceutical projects, ensuring they are completed on time, within scope, and on budget. This role involves managing cross-functional teams, planning project timelines, handling risks, and ensuring compliance with regulatory standards. Pharma Project Managers often work closely with research and development, clinical, regulatory, and manufacturing teams to bring new drugs or treatments to market efficiently and safely. Their responsibilities also include stakeholder communication and resource management throughout the project lifecycle.

How does a Pharma Project Manager typically collaborate with cross-functional teams throughout a drug development project?

A Pharma Project Manager plays a central role in coordinating cross-functional teams, including research, clinical, regulatory, and manufacturing departments. They facilitate regular meetings, ensure clear communication of project goals, and address any obstacles that arise. Effective Pharma Project Managers build strong relationships with team members, align timelines, and manage resources to keep projects on track. This collaborative approach is essential for navigating the complexities of drug development and meeting regulatory and company milestones.

What are the key skills and qualifications needed to thrive as a Pharma Project Manager, and why are they important?

To thrive as a Pharma Project Manager, you need strong project management expertise, knowledge of pharmaceutical regulations, and a background in life sciences or a related field. Familiarity with project management tools (such as Microsoft Project or Smartsheet), regulatory compliance systems, and certifications like PMP or PRINCE2 are commonly required. Exceptional organizational skills, problem-solving ability, and effective communication help you excel when coordinating cross-functional teams and managing complex timelines. These skills are crucial for ensuring projects are delivered on time, on budget, and in compliance with industry standards.

What is the difference between Pharma Project Manager vs Clinical Research Associate?

AspectPharma Project ManagerClinical Research Associate
CredentialsBachelor's or higher in life sciences, PMP certification often preferredBachelor's in life sciences, relevant clinical research certifications
Work EnvironmentCoordinates multiple projects across departments in pharmaceutical companiesMonitors clinical trial sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, biotech firmsContract research organizations, clinical trial sites

While both roles are essential in the pharmaceutical industry, a Pharma Project Manager oversees multiple projects and teams, focusing on planning and execution, whereas a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity.

How much do pharmaceutical project managers make in the US?

Pharmaceutical project managers in the US typically earn between $90,000 and $130,000 annually, with salaries varying based on experience, location, and company size. Senior roles or those with specialized skills and certifications can earn higher compensation, often exceeding $150,000 per year.

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

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

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

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

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

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

Pharma Project Manager jobs near you
Infographic showing various Pharma Project Manager job openings in Minnesota as of August 2026, with employment types broken down into 86% Full Time, 9% Part Time, and 5% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $94,204 per year, or $45.3 per hour.

Senior R&D Engineer

Stark Pharma Solutions Inc

Minneapolis, MN • On-site

$109K - $149K/yr

Contractor

Re-posted 20 days ago

Job description

Hello Professionals,

This is Karthik Mutyala from Stark Pharma. We are currently hiring for a Senior R&D Engineer opportunity with one of our medical device clients in the greater Minneapolis area. This is a long-term onsite opportunity running through the end of 2026 with a strong possibility of extension.

Position: Senior R&D Engineer

Location: Greater Minneapolis Area (Onsite – 4 days/week)

Duration: Through End of 2026 (Possible Extension)

Key Responsibilities:

  • Lead integration-focused design and development activities for new and existing medical device technologies
  • Drive interface definition, technical planning, requirements alignment, and integration execution
  • Own design control documentation including DHF, traceability, risk management, V&V, and change control activities
  • Support feasibility studies, prototype builds, testing, and design optimization
  • Conduct root cause analysis and resolve complex technical issues
  • Collaborate with Quality, Manufacturing, Regulatory, and Supplier Engineering teams to ensure successful project execution

Required Qualifications:

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Materials Science, or related field
  • 6+ years of industry experience (or 4+ years with advanced degree)
  • Experience in catheter and/or single-use medical device development
  • Strong understanding of design controls, risk management, V&V, DHF, and traceability
  • Proven experience leading technical workstreams and working cross-functionally
  • Strong communication and problem-solving skills
  • Ability to travel up to 15%

Preferred Qualifications:

  • Experience with technology/product integration projects
  • Background in balloon catheter or catheter-based systems
  • Experience with test method development
  • Knowledge of Class II/III medical device regulations and quality systems
  • Self-driven professional comfortable working in fast-paced environments

Interested candidates can share their updated resume.

If you are not interested, please feel free to refer your friends or colleagues who may be looking for an opportunity.