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Project Manager Biotech Jobs in Minnesota (NOW HIRING)

Actalent

Senior Project Coordinator

Hopkins, MN

Manage preventive maintenance, calibration, validation, and vendor service schedules, communicate ... Proven experience working within GMP-regulated environments in pharmaceutical, biotech, or medical ...

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Project Manager Biotech information

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$45

$74

How much do project manager biotech jobs pay per hour?

As of Jul 16, 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, and why are they important?

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 July 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 II

Bora Pharmaceuticals

Maple Grove, MN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 21 hours ago

Job description

About Bora
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora's teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer's success more certain.
Job Summary
The Project Manager II provides dedicated, cross-functional project management of development, technical transfer, operational activities that supports the product lifecycle within the manufacturing site (e.g., purchase orders, forecasting schedules, change orders, invoicing, and shipping project management activities). The role executes a client engagement model and governance, assures effective and routine open communications and relationship management discussions with internal functional groups, as well as external client groups. The Project Manager is responsible for ensuring project milestones and budget are met, including ensuring pass through and change order costs are accounted for. The role is vital to business and development/tech transfer growth at the site. The person in this role integrates their understanding and knowledge of technical, financial and commercial needs to ensure projects run smoothly.
The Project Manager is expected to be on-site a minimum of three to four days per week, with additional consideration to prioritize client visits and other client-engaging requests, and in accordance with business needs.
Essential Job Duties
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
  • In the PDS department, this role would support timelines during the quotation process and engage with BD early-on to ensure successful handoff when contract is signed.
  • This individual will help with organizing client visits, both from a due diligence and person in plant prospective.
  • This person has a significant role in ensuring financial forecasting and invoicing are as planned, and if not ensures there is a contingency plan to catch up.
  • Managing and forecasting project budgets and ensuring change orders are passed on in a timely manner are critical to this job function.
  • Manages both internal and external team meetings for assigned clients. Provides constant feedback and fast turnaround to internal and external partners.
  • Executes client communications, associated with routine engagement, messaging, escalation, and notifications.
  • Manages and executes appropriate escalation for client matters within the PDS Management Team, appropriate functions, site leadership and the CDMO BU.
  • Serves as site operations business manager, working with site and Supply Chain leadership to:
  • Assure client support prioritization alignment with product forecast and production priorities
  • Manage Client inventory position, communicate Client's product necessity in market and their relevant business strategies and plans
  • Facilitate efforts of Ambassador team to deliver highest levels of service, attention to client inquires, escalation and needs for existing business
  • Assure connection and information sharing across site functions and with CDMO BU.
  • Coordinates efforts to facilitate client product handoff from new product introduction and qualification activities to run-the-business portfolio management duties.
  • Orchestrates and assures close management and execution of improve-the-business activity (continuous improvement, deviation investigation and corrective / preventative action efforts) with assigned Clients.
  • Executes highly effective routines, tools, templates, and associated guidance for business meeting preparation, setting agendas, and associated standard work which aid client engagement experience.
  • Works to ensure safe and compliant execution of activities, including collaboration with EH&S for client safety when on site.
  • Executes goals and accountabilities based on agreed objectives and results.
  • Collaborate and communicate with other functional areas to promote understanding and achieve strategic objectives.
  • Promptly notifies management, the team and Quality leadership of potential issues or problems.

Minimum Education / Experience Requirements
  • B.S / B.A. degree in Project Management, Business or a related pharmaceutical sciences field. PMP certification preferred.
  • 6+ years cGMP experience in solid oral dose pharmaceutical (preferred), biotech or bio-pharmaceutical manufacturing environment, ideally pre-clinical phases to commercial, and / or equivalent amount of experience managing commercial operations or client portfolio management roles.
  • Comprehensive understanding of finance - invoicing, financial forecasting, and impact of planning in pharmaceutical or bio-pharmaceutical manufacturing operations.
  • 6+ years' experience and strength in planning, orchestrating, and managing business critical relationships between providers / suppliers and clients.
  • Experience working with FDA (Food and Drug Administration) and participating in regulatory agency inspections desirable.
  • Strong interpersonal and collaborative / facilitative skills across functions, across internal business enterprise, and externally with multiple clients within a portfolio.
  • Proven, effective communication skills, oral and written, ability to drive and be assertive.
  • Ability to work independently and in a team setting with minimal supervision.
  • Ability to make sound decisions regarding compliance-related issues with minimal supervision; proactive in identifying risks and creating mitigation plans.
  • Demonstrated, proven record of personal accountability and responsibility with a delivery-focused mindset.

The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time which reflects management's assignment of essential functions.
Compensation Range
$108,000 - $150,000
Compensation and Benefits
We offer a comprehensive benefits package designed to support our employees' wellbeing, including:
  • Competitive salary and performance-based incentives
  • Comprehensive health coverage including medical, dental, and vision insurance
  • Retirement savings plans with employer matching contributions
  • Paid time off
  • Professional development opportunities
  • Employee wellness programs and resources
  • Employee Assistance Program and Mental Health Resources

Core Values
At Bora, our values guide everything we do - from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone.
Bora Pharmaceuticals is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Bora Pharmaceuticals will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category.

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