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Biopharma Project Manager Jobs (NOW HIRING)

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BAS Project Manager

Houston, TX · On-site

$100K - $125K/yr

... Biopharma, Mission Critical, Entertainment Services Provided: * Building Automation Systems ... Manage BAS projects from kickoff through final completion * Review drawings, project specifications ...

ABEC Inc

Project Manager

Wilson, NC · On-site

For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry ... The Project Manager is responsible for all aspects of assigned jobs from notice to start, until ...

ABEC Inc

Project Manager

Wilson, NC · On-site

For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry ... The Project Manager is responsible for all aspects of assigned jobs from notice to start, until ...

ABEC Inc

Project Manager

Wilson, NC · On-site

For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry ... The Project Manager is responsible for all aspects of assigned jobs from notice to start, until ...

E Tech Group

Project Manager

Albany, NY · On-site

Understanding of Biopharmaceutical processes * Understanding of control system network topology ... Experience managing projects in regulated/GxP environments * Knowledge of S88 Batch standards and ...

E Tech Group

Project Manager

Albany, NY · On-site

Understanding of Biopharmaceutical processes * Understanding of control system network topology ... Experience managing projects in regulated/GxP environments * Knowledge of S88 Batch standards and ...

E Tech Group

Project Manager

Albany, NY

Understanding of Biopharmaceutical processes * Understanding of control system network topology ... Experience managing projects in regulated/GxP environments * Knowledge of S88 Batch standards and ...

Advanced Bio-Logic Solutions Corp.

$75 - $82/hr

... biopharma leader. Oversee all phases of the project lifecycle, aligning scope, time, cost, and quality requirements with business objectives. Collaborate closely with senior management and cross ...

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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 Jun 14, 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 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 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.
Infographic showing various Biopharma Project Manager job openings in the United States as of June 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $96,560 per year, or $46.4 per hour.

Construction Project Manager

GenScript/ProBio

Piscataway, NJ

$120K - $150K/yr

Full-time

Posted 21 days ago

Job description

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

Job Title: Construction Project Manager

Location: Piscataway, NJ (Fully onsite)

Reports to: Director of US Site Operations

Compensation: The estimated salary range is $120,000 - $150,000, based on experience.

Overview:

GenScript is seeking a talented, detail oriented and self-driven individual to join the Operations Department, contributing to the planning, design, construction, commissioning, validation, and engineering process systems development for our facilities in Piscataway, NJ. This position is valid for at least 1-2 years with the opportunity to transition to facility manager after the construction projects are done.

Job Responsibilities:

Project Planning and Execution:

  • Develop comprehensive project plans ensuring projects proceed according to set objectives, including requirement gathering, feasibility analysis, risk assessment, and solution formulation.
  • Manage cost estimation for all project phases and create cost control plans.
  • Procurement and Contract Management.
  • Oversee bidding and procurement for project design, construction, and long-lead equipment.
  • Manage contract signing and execution with suppliers and contractors, ensuring compliance with terms, quality, and deadlines.

Compliance and Regulatory Affairs:

  • Plan and execute government and third-party procedures to ensure project compliance with US regulations.
  • Plan and manage government permits applications.

Project Management:

  • Manage technical, quality, safety, and timeline aspects of projects, ensuring timely resolution of technical issues, compliance with quality standards, and implementation of safety measures.
  • Coordinate with construction firms, supervisory, and contracting units to manage internal and external project relationships.
  • Commissioning and Validation:
  • Organize factory acceptance tests, commissioning, and validation to ensure systems meet user requirements.

Project Completion:

  • Lead the final inspection, handover, documentation review, and project settlement activities, ensuring successful project completion and handover.
  • Reporting and Improvement:
  • Regularly report project progress, compile project reports, analyze lessons learned, and suggest improvements.

Qualifications and Requirements

Education and Experience:

  • Bachelor's degree or higher in Mechanical/Electrical, Chemical Engineering, Biomedical Engineering, or related fields.
  • 10+ years of experience in biopharmaceuticals with substantial project management and facility operations experience.
  • Hands on experience in managing construction, experience in executing projects from business requirement collection through to design, construction, commissioning, validation, and final settlement is preferred.

Skills:

  • Strong management and reporting capabilities, clear management vision, able to handle high-pressure work environments.
  • Solid technical expertise combined with engineering knowledge.
  • Demonstrated skills in problem solving, root cause analysis with result driven thought process.

Additional Considerations:

  • Proficient in project management software (e.g., Procore, Microsoft Project, Primavera P6).
  • Familiarity with construction estimating and scheduling tools.
  • Understanding of US building codes, zoning laws, safety regulations, and biopharmaceutical industry standards.

#LI-EB1

#GS

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.