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Pharmaceutical Project Manager Jobs in Minnesota

DDL, Inc.

Packaging Project Manager

Eden Prairie, MN · On-site

$30 - $33/hr

This entry level Packaging Project Manager role is the perfect opportunity for individuals who are ... DDL, Inc. is a third-party testing facility dedicated to helping medical device and pharmaceutical ...

E*Pro, Inc.

PMO Lead

Minneapolis, MN · On-site

... Pharmaceutical, Health Care and service industries ensures our services are customized to meet ... manager requirements forecasting (Ramp up/down) Project Metrics and reporting PMO Process gaps and ...

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Pharmaceutical Project Manager information

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$44.1K

$102.9K

$166K

How much do pharmaceutical project manager jobs pay per year?

As of Aug 13, 2026, the average yearly pay for pharmaceutical project manager in Minnesota is $102,864.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,300.00 and $125,900.00 per year, depending on experience, location, and employer.

What is a pharmaceutical project manager?

A Pharmaceutical Project Manager oversees drug development projects from initiation to completion, ensuring they meet regulatory, budget, and timeline requirements. They coordinate cross-functional teams, including researchers, regulatory specialists, and manufacturing professionals, to bring pharmaceutical products to market. Their responsibilities include risk management, resource allocation, and stakeholder communication. Strong project management skills, industry knowledge, and attention to compliance are essential for success in this role.

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

A Pharmaceutical Project Manager needs a strong background in life sciences or pharmaceuticals, experience in project management, and often a relevant degree or certification such as PMP. Familiarity with tools like Microsoft Project, regulatory compliance systems (e.g., FDA or EMA guidelines), and document management platforms is crucial. Excellent communication, leadership, problem-solving, and organizational abilities set standout candidates apart. These skills are vital to effectively lead cross-functional teams, ensure regulatory compliance, and successfully deliver projects on time and within budget in a complex industry.

What are the main challenges a pharmaceutical project manager faces during a drug development project?

Pharmaceutical Project Managers often encounter challenges such as navigating complex regulatory requirements, managing tight project timelines, and coordinating across multiple departments like clinical research, regulatory affairs, and manufacturing. Ensuring effective communication among diverse stakeholders and addressing unforeseen obstacles, such as changes in trial protocols or supply chain disruptions, are also common. Strong organizational and leadership skills are essential for adapting to evolving project demands and keeping teams aligned. By anticipating challenges and fostering collaboration, Pharmaceutical Project Managers help ensure successful project outcomes and regulatory approvals.

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

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

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

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

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

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

Pharmaceutical Project Manager jobs near you
Infographic showing various Pharmaceutical Project Manager job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 10% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $102,864 per year, or $49.5 per hour.

Project Manager II

Bora Pharmaceuticals

Maple Grove, MN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 28 days 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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