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Biopharma Project Manager Jobs (NOW HIRING)

Project Manager

Bothell, WA · On-site

$94K - $129K/yr

... biopharmaceutical, biotechnology, or CDMO environments. * 2-5 years of direct project management ... experience. * Strong knowledge of GMP regulations and regulated manufacturing environments.

NY · On-site

Responsible for designing and implementing projects, milestone follow-up, completion of data ... D. in Biomedical / Biopharmaceutical / Molecular biology / Cellular biology / Biomedical ...

Description: Project Manager - Engineering and Life Sciences Equipment Join a team delivering ... For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry.

Job Type Full-time Description Project Manager - Engineering and Life Sciences Equipment Join a ... For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry.

Description Project Manager - Engineering and Life Sciences Equipment Join a team delivering ... For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry.

Project Manager - Engineering and Life Sciences Equipment Join a team delivering critical equipment ... For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry.

Project Manager - Engineering and Life Sciences Equipment Join a team delivering critical equipment ... For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry.

Project Manager - Engineering and Life Sciences Equipment Join a team delivering critical equipment ... For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry.

Senior Project Manager

Redmond, WA · On-site

$60K - $85K/yr

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... We are seeking a Senior Project Manager, R&D to support cross-functional planning and execution for ...

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Biopharma Project Manager information

See salary details

$44.5K

$96.6K

$154.5K

How much do biopharma project manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for biopharma project manager in the United States is $96,560.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $113,000.00 per year, depending on experience, location, and employer.

What does a biopharma project manager do?

A Biopharma Project Manager oversees the planning, execution, and completion of projects within the biopharmaceutical industry. They coordinate cross-functional teams, manage timelines and budgets, and ensure that project goals align with regulatory requirements and company objectives. Their role is critical for bringing new drugs and therapies from development to market efficiently while maintaining compliance and quality standards.

What are some common challenges biopharma project managers face when coordinating cross-functional teams?

Biopharma Project Managers frequently encounter challenges in aligning the goals and timelines of diverse teams such as R&D, regulatory affairs, clinical operations, and manufacturing. These teams often have different priorities and work rhythms, which can create communication gaps or delays. Effective project managers proactively facilitate clear communication, set realistic expectations, and regularly update stakeholders to ensure everyone is moving toward shared project milestones. Building strong relationships and fostering a collaborative environment are crucial for overcoming these hurdles and driving projects to successful completion.

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

To thrive as a Biopharma Project Manager, you need a solid background in life sciences or pharmaceutical development, project management expertise, and often a relevant degree such as a PMP certification or advanced scientific degree. Familiarity with project management tools (like MS Project or Smartsheet), regulatory systems (such as FDA or EMA guidelines), and budgeting software is typically required. Excellent communication, leadership, and problem-solving skills are crucial for managing cross-functional teams and ensuring project milestones are met. These competencies are vital for delivering complex projects on time and within budget, while ensuring compliance and fostering innovation in a highly regulated industry.

What is the difference between Biopharma Project Manager vs Clinical Research Coordinator?

AspectBiopharma Project ManagerClinical Research Coordinator
CredentialsTypically requires a bachelor’s degree in life sciences, project management certification (e.g., PMP)Usually holds a bachelor’s degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentManages projects across departments in biotech or pharmaceutical companiesWorks directly on clinical trial sites, coordinating patient recruitment and data collection
Employer & IndustryBiotech, pharmaceutical companies, contract research organizationsHospitals, clinical research organizations, academic medical centers

The Biopharma Project Manager oversees the planning and execution of biopharmaceutical projects, focusing on timelines, budgets, and team coordination. In contrast, the Clinical Research Coordinator handles the day-to-day operations of clinical trials, ensuring compliance and data accuracy. Both roles require knowledge of clinical processes but differ in scope and responsibilities.

What are popular job titles related to Biopharma Project Manager jobs?

For Biopharma Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Biopharma Project Manager job openings in the United States as of September 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $96,560 per year, or $46.4 per hour.

Project Manager

Bothell, WA • On-site

AGC Biologics
Biotechnology Research and Development • 1 - 5K employees

$94K - $129K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 25 days ago


Key responsibilities

  • Lead biologics programs across the full product lifecycle, including technology transfer, process development, and GMP manufacturing.

  • Develop and maintain project plans to ensure delivery within scope, timeline, and budget, and serve as the primary point of contact for clients.

  • Identify project risks, develop mitigation strategies, and facilitate issue resolution with functional leaders.


AGC Biologics rating

7.5

Company rating: 7.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz


Job description

Join Us in Bringing Hope to Life

Our purpose is to bring hope to life by enabling lifechanging therapies for patients around the globe, creating a healthier and happier tomorrow. To advance this purpose, we rely on team members who value excellence, collaboration, and meaningful work. If this resonates with you, we invite you to explore the role further and apply.

Job Summary

We are looking for a Project Manager to lead biologics programs across the full product lifecycle, from technology transfer and process development through GMP manufacturing. This role is responsible for delivering projects on time, within scope, and within budget while ensuring alignment with client expectations and regulatory requirements.

About the Team

You will join a Program Management team responsible for leading client programs and coordinating activities across Process Development, Manufacturing, Quality, MSAT, Analytical, Regulatory, and Supply Chain functions. The team plays a critical role in ensuring successful program delivery while maintaining strong client relationships and supporting business growth.

Key Responsibilities

  • Lead CMC development, technology transfer, and GMP manufacturing programs from project initiation through close-out.

  • Develop and maintain project plans to ensure delivery within scope, timeline, and budget.

  • Serve as the primary point of contact for clients, providing clear communication and program leadership.

  • Partner with Business Development to strengthen client relationships and support program growth.

  • Identify project risks, develop mitigation strategies, and facilitate issue resolution with functional leaders.

  • Establish contingency plans and escalate critical issues as needed.

  • Drive alignment across Process Development, Analytical, QC, QA, MSAT, Supply Chain, and Manufacturing teams.

  • Support late-stage activities including PPQ readiness, regulatory submissions, and commercialization efforts.

  • Apply technical understanding of biologics development and manufacturing to support decision-making and technology transfer activities.

  • Manage project financials and contractual commitments, including Project Change Orders.

  • Provide milestone updates and forecasting information to support financial planning and client invoicing.

Skills

  • Strong written and verbal communication skills with the ability to engage senior stakeholders and clients.

  • Ability to lead and influence cross-functional teams without direct authority.

  • Strong problem-solving, decision-making, and conflict resolution skills.

  • Financial acumen, including experience managing budgets, contracts, and invoicing processes.

  • Strong planning, organization, and project execution capabilities.

Qualifications & Experience

Required:

  • Bachelor's degree in Life Sciences, Chemistry, Biotechnology, Engineering, or a related field.

  • 3-8 years of experience within biopharmaceutical, biotechnology, or CDMO environments.

  • 2-5 years of direct project management experience.

  • Strong knowledge of GMP regulations and regulated manufacturing environments.

  • Experience with project management tools such as PPM systems or Smartsheet.

Preferred:

  • 2+ years of CDMO experience.

  • Experience supporting late-stage programs, including PPQ, BLA preparation, and commercialization activities.

  • Experience leading technology transfers and new product introductions.

  • Familiarity with TrackWise.

Formalities

Location: Bothell, WA

Schedule: Full-time

Compensation: $94,000 - $129,250


We offer a comprehensive Total Rewards package that may include annual bonus opportunities, paid time off, medical, dental and vision coverage, parental leave, education assistance, employee referral and recognition programs, and additional wellbeing benefits. Eligibility and benefits may vary based on role, location, and employment status.
Who We Are

AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in the United States. From our headquarters in Bothell, Washington, we develop and manufacture lifechanging advanced biologics for some of the world's most innovative pharmaceutical companies. Together with our team members across Europe, the U.S., and Japan, we deliver development and manufacturing of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells therapies. Across our global network, we are united by one mission: To work side by side with our customers in order to improve patients' lives by bringing new biopharmaceuticals to market.

We are a collaborative, inclusive, and equalopportunity organization where team members are valued for their expertise, teamwork, and ingenuity.


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