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Project Manager Biotech Jobs in Minnesota (NOW HIRING)

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 ...

Celcuity Inc.

Lab Systems Manager

Minneapolis, MN · On-site

$90K - $125K/yr

Project Management : Lead facility upgrades, lab expansions, and equipment or lab operations ... Celcuity is a commercial biotechnology company pursuing development of targeted therapies for ...

Celcuity Inc.

Lab Systems Manager

Minneapolis, MN · On-site

$90K - $125K/yr

Project Management : Lead facility upgrades, lab expansions, and equipment or lab operations ... Celcuity is a commercial biotechnology company pursuing development of targeted therapies for ...

Harvard Bioscience

Quality Manager ISO9001

Saint Paul, MN · On-site

$110K - $160K/yr

... pharmaceutical, biotechnology and clinical research organizations.POSITION SUMMARY Harvard ... Plans and leads improvement projects.Quality: Leads execution of the Global Quality Plan in ...

Harvard Bioscience

Quality Manager ISO9001

Saint Paul, MN · On-site

$110K - $160K/yr

... pharmaceutical, biotechnology and clinical research organizations. POSITION SUMMARY Harvard ... Plans and leads improvement projects. Quality: * Leads execution of the Global Quality Plan in ...

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Showing results 21-40

All JobsProject Biotech JobsProject Manager Biotech JobsProject Manager Biotech Jobs in Minnesota

Project Manager Biotech information

See Minnesota salary details

$21

$45

$74

How much do project manager biotech jobs pay per hour?

As of Aug 7, 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 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.

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 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.
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.

Cleaning Validation Engineer

PSC Biotech

Minneapolis, MN • On-site

$90K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.

Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success.

The Experience

With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.

At PSC Biotech®, it’s about more than just a job—it’s about your career and your future.

Your Role

The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing operations. This role will focus on cleaning validation for production equipment, including harvest centrifuges and production bioreactors, ensuring compliance with GMP requirements and client quality standards. The engineer will author, execute, and route validation protocols within Kneat, perform on-site sampling activities, and support the successful completion of cleaning validation deliverables.
  • Develop, modify, execute, and manage cleaning validation protocols for harvest centrifuges, production bioreactors, and associated manufacturing equipment.
  • Generate cleaning validation reports, ensuring accurate documentation of execution results and conclusions.
  • Author, execute, review, and route validation protocols within Kneat.
  • Perform on-site protocol execution activities, including swab and rinse sampling.
  • Coordinate sampling activities and ensure adherence to approved protocols and site procedures.
  • Support investigation and resolution of protocol discrepancies, deviations, and documentation issues.
  • Maintain complete and accurate validation documentation in accordance with GMP requirements and client procedures.
  • Collaborate with Quality, Manufacturing, Engineering, and Validation teams to support project timelines and deliverables.
  • Ensure compliance with established cleaning validation strategies, acceptance criteria, and quality systems.
  • Complete all required site training and adhere to site-specific safety, quality, and operational standards.


Requirements
  • Bachelor's degree in Engineering, Biology, Chemistry, Life Sciences, or a related technical discipline.
  • 3+ years of experience in Cleaning Validation, CQV, Validation, or Quality Engineering within the pharmaceutical, biotechnology, or life sciences industry.
  • Hands-on experience developing, modifying, and executing cleaning validation protocols.
  • Experience performing swab and rinse sampling activities in a GMP manufacturing environment.
  • Experience with cleaning validation of centrifuges, bioreactors, CIP systems, and process equipment.
  • Experience generating and reviewing validation reports and supporting documentation.
  • Strong understanding of GMP regulations, validation lifecycle principles, and documentation practices.
  • Kneat experience is required, including protocol authoring, execution, review, and routing.
  • Ability to work on-site and support execution activities in manufacturing environments.
  • Strong technical writing, communication, and organizational skills.
  • Must be authorized to work in the U.s.
  • No C2C at this time.

Benefits
Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.
  • Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
  • Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more.
  • 401(k) and 401(k) matching
  • PTO, Sick Time, and Paid Holidays
  • Education Assistance
  • Pet Insurance
  • Fitness Benefits (Membership discounts and other perks/services at qualifying gyms like Anytime Fitness, 24-Hour Fitness, and more)
  • Financial Perks and Discounts
The salary bracket for this role is set between $90,000 - $105,000 annually. The salary offered may be adjusted based on various factors such as the applicant's qualifications, skills, and professional experience.

Equal Opportunity Employment Statement

PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.

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