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Biotechnology Project Manager Jobs in Minnesota (NOW HIRING)

Sr Process Engineer

Brooklyn Park, MN · On-site

$108K - $140K/yr

Serve as project manager on small to medium projects under $5M * Interface with cross-functional ... Experience in pharmaceutical or biotechnology manufacturing environment * Engineer-in-Training (EIT ...

Sr Process Engineering

Brooklyn Park, MN · On-site

$108K - $140K/yr

Serve as project manager on small to medium projects under $5M * Interface with cross-functional ... Experience in pharmaceutical or biotechnology manufacturing environment * Engineer-in-Training (EIT ...

Clinical Trial Manager

Minneapolis, MN · On-site

$108K - $162K/yr

This position will also oversee project management and will delegate tasks to the clinical team ... Bachelor's degree (preferably in health science or biotech area) * Experience with clinical trial ...

Clinical Trial Manager

Minneapolis, MN · On-site

$108K - $162K/yr

This position will also oversee project management and will delegate tasks to the clinical team ... Bachelor's degree (preferably in health science or biotech area) * Experience with clinical trial ...

Quality Manager

Glencoe, MN · On-site

$90K - $105K/yr

Project Management and problem solving skills. * Knowledge of risk assessments and risk management ... Cook Biotech in IN. and Collagen Solutions, MN. Our new brand identity emphasizes our unique ...

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking ...

Clinical Study Manager

Fridley, MN · On-site

$110K - $160K/yr

... biotechnology, or pharmaceutical industries * 3+ years of clinical study management or clinical ... Highly organized with strong project management and prioritization skills * A collaborative team ...

Showing results 41-60

Biotechnology Project Manager information

See Minnesota salary details

$21

$45

$74

How much do biotechnology project manager jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for biotechnology 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 biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.
What are popular job titles related to Biotechnology Project Manager jobs in Minnesota? For Biotechnology Project Manager jobs in Minnesota, the most frequently searched job titles are:
What cities in Minnesota are hiring for Biotechnology Project Manager jobs? Cities in Minnesota with the most Biotechnology Project Manager job openings:
Infographic showing various Biotechnology Project Manager job openings in Minnesota as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $94,204 per year, or $45.3 per hour.

Sr Process Engineer

Takeda

Brooklyn Park, MN • On-site

$108K - $140K/yr

Full-time

Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job DescriptionAbout the Role:

Serve as the Engineering subject matter expert for a specific process area (cell culture, harvest, purification, clean-in-place, or utilities systems)

Ensure systems remain in a qualified state. Act as technical owner for system lifecycle including design, installation, qualification, production support, deviation resolution, maintenance, and decommissioning

Monitor system reliability and performance. Develop and implement engineering solutions to complex problems. Lead programs related to system qualification, asset management, project execution, and Good Engineering Practices. Support development of site staff on technical and procedural topics

How you will contribute:
  • Develop engineering deliverables including Process Flow Diagrams, P&IDs, System Specifications, and Functional Specifications
  • Implement system modifications under cGMP change control
  • Develop and execute FAT, commissioning protocols, and qualification protocols
  • Develop calibration and preventative maintenance plans
  • Lead deviation investigations and implement corrective and preventative actions
  • Participate in capital planning, spending, and tracking
  • Serve as project manager on small to medium projects under $5M
  • Interface with cross-functional teams to meet project goals
  • Stay current with industry best practices and technologies
  • Complete required training within timeframe
  • Selecting technologies, designing equipment, and diagnosing process issues
  • Making data-driven decisions using engineering principles
  • Ensuring impact to product quality, safety, reliability, and throughput
  • Maintaining regulatory compliance and validation requirements
  • Troubleshooting factory floor issues and supporting capacity planning
  • Managing impact to uptime, batch continuity, and manufacturing schedule
  • Responding to urgency and severity of equipment failures
  • Determining escalation thresholds
  • Balancing short-term mitigation versus long-term solutions
  • Perform other duties as assigned
What you bring to Takeda:
  • Bachelor's degree in Engineering
  • 3 or more years of relevant experience
  • Experience in pharmaceutical or biotechnology manufacturing environment
  • Engineer-in-Training (EIT) or Professional Engineer license preferred
  • Demonstrated track record supporting process operations and projects in an FDA-regulated environment
  • Knowledge of engineering principles including fluid mechanics, heat transfer, thermodynamics, and mass transfer
  • Experience applying project management methodologies
  • Understanding of commissioning and qualification protocol development
  • Direct experience with systems such as bioreactors, centrifugation, chromatography, tangential flow filtration, CIP, autoclaves, clean utilities, and HVAC
  • Familiarity with instrumentation and sensing technologies in pharmaceutical manufacturing
  • Experience with regulatory requirements and GMP environments
  • Experience supporting large capital projects
  • Familiarity with batch control systems, data historians, SQL, and scripting (preferred)
  • Knowledge of automation, PLCs, power systems, and controls (desirable)
  • Proficient in MS Office (Word, Excel, PowerPoint) and MS Project
  • Ability to work in fast-paced, cross-functional teams
  • Strong planning, prioritization, and escalation judgment
Important Considerations

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:

  • Combination of sedentary work and facility walkdowns
  • Occasional ladder climbing
  • Ability to lift up to 25 lbs
  • Participation in 24/7 on-call rotation
  • Use of PPE and clean room garments as required
  • Infrequent travel up to approximately 25% during project activities
More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

#GMSGQ #ZR1 #LI-Onsite

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

Brooklyn Park, MN

U.S. Base Salary Range:

$89,900.00 - $141,240.00


The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

LocationsBrooklyn Park, MNWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Job Exempt

Yes