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Biotechnology Project Manager Jobs in Worcester, MA

Syner-G

Sr. Project Engineer

Marlborough, MA · On-site

$102K - $133K/yr

Generate and manage engineering and validation lifecycle documentation, including impact ... biotechnology, or industrial environment. * Experience supporting capital projects within GMP ...

Socket.dev

Sr. Project Engineer

Marlborough, MA · On-site

$125 - $150/hr

Through our expertise, insight, consulting and management skills, we accelerate breakthrough ... biotechnology, or industrial environment. * Experience supporting capital projects within GMP ...

New

Syner-G

Sr. Project Engineer

Marlborough, MA · On-site

$102K - $133K/yr

Through our expertise, insight, consulting and management skills, we accelerate breakthrough ... biotechnology, or industrial environment. * Experience supporting capital projects within GMP ...

Syner-G

Sr. Project Engineer

Marlborough, MA · On-site

$102K - $133K/yr

Through our expertise, insight, consulting and management skills, we accelerate breakthrough ... biotechnology, or industrial environment. * Experience supporting capital projects within GMP ...

YMC America Inc

SENIOR ACCOUNT MANAGER

Harvard, MA · On-site

$125 - $150/hr

The Senior Account Manager partners closely with engineering, applications, project management, and ... Prospect targeted biopharmaceutical manufacturers, CDMOs, and biotechnology companies to generate ...

YMC America Inc

SENIOR ACCOUNT MANAGER

Devens, MA · On-site

$135K - $160K/yr

The Senior Account Manager partners closely with engineering, applications, project management, and ... Prospect targeted biopharmaceutical manufacturers, CDMOs, and biotechnology companies to generate ...

YMC America Inc

SENIOR ACCOUNT MANAGER

Devens, MA · On-site

$135K - $160K/yr

The Senior Account Manager partners closely with engineering, applications, project management, and ... Prospect targeted biopharmaceutical manufacturers, CDMOs, and biotechnology companies to generate ...

DPS Group

Electrical Engineer

Framingham, MA · On-site

Develop technical specifications and layouts while working in tandem with project managers and ... biotech, pharma, or Life sciences industries. * Strongly motivated, well organized, and shows ...

AT Process Technologies

Project Engineer

Waltham, MA · On-site

$100K - $180K/yr

You'll also aid in managing the project itself, helping keep scope, timelines, and priorities on ... Background in energetics, chemicals, process/manufacturing, biotech/pharma, or another regulated ...

AT Process Technologies

Project Engineer

Waltham, MA · On-site

$80 - $100/hr

You'll also aid in managing the project itself, helping keep scope, timelines, and priorities on ... Background in energetics, chemicals, process/manufacturing, biotech/pharma, or another regulated ...

Rentschler

Proposal Manager

Milford, MA · On-site

Degree in Life Sciences, Biotechnology, Biochemical Engineering, or a related field * 3+ years of experience in proposal management, technical project management, or a comparable role within the ...

RoslinCT US

Program Manager

Hopkinton, MA · On-site

Bachelor's degree in biotechnology related degree or equivalent * 5+ years of upper management experience * 5+ years of direct client facing project/program management experience * 7+ years working ...

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All JobsBiotechnology Project JobsBiotechnology Project Manager JobsBiotechnology Project Manager Jobs in Worcester, MA

Biotechnology Project Manager information

See Worcester, MA salary details

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$46

$76

How much do biotechnology project manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for biotechnology project manager in Worcester, MA is $46.14, according to ZipRecruiter salary data. Most workers in this role earn between $40.05 and $50.62 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

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

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Biotechnology Project Manager jobs in Worcester, MA?

For Biotechnology Project Manager jobs in Worcester, MA, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Worcester, MA look for?

The top searched job categories for Biotechnology Project Manager jobs in Worcester, MA are:

What cities near Worcester, MA are hiring for Biotechnology Project Manager jobs?

Cities near Worcester, MA with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Worcester, MA as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, and 3% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $95,975 per year, or $46.1 per hour.

Consultant, Life Sciences - Pharmaceuticals

Integrated Project Management Company

Maynard, MA • On-site

Full-time

Medical, PTO

Re-posted 17 days ago

Job description

For more than three decades, premier organizations have trusted IPM to lead the successful execution of their strategic portfolios and critically important initiatives.  Headquartered in Chicago with offices in Boston, Parsippany, Minneapolis, St. Louis, Los Angeles, and San Francisco, IPM has led more than 5,000 projects for over 500 clients.  Our clients range from Fortune 100 companies to start-ups.
 
We are a certified “Great Place to Work” company and have been named to the Great Place to Work list of “Best Workplaces in Consulting and Professional Services”.
 
Our Consultants are our full-time employees and the competitive advantage that sets us apart from the rest. 

IPM partners with clients across the life sciences industry sectors, including pharmaceuticals, medical technology, and biotechnology, which includes large-molecule proteins, monoclonal antibodies, cell, tissue, and genetic therapies, and molecularly engineered vaccines.  
 
Within each sector we lead, at the core team level, product development projects from pre-clinical R&D through commercialization, including planning for regulatory, clinical, and commercial strategies and processes, and product lifecycle management with a focus to late stage development and submission. 

Within each sector we lead the creation or improvement of operational processes including harmonizing regulatory and quality systems and building project, program and portfolio management capabilities.
 
JOB DESCRIPTION 
As a Consultant, you will partner with client leadership and delivery teams to lead project and program planning and execution across various functions, driving projects and programs to achieve mission-critical outcomes for our pharmaceutical industry clients.  At each new engagement you will leverage the continual exposure and experiences from working within a variety of clients and project types. 
 
Your primary goals and focus will be to: 
  • Lead product development projects and programs in the pharmaceutical industry, including pre-clinical R&D, commercialization and product lifecycle management
  • Implement or optimize project management frameworks through the use of current best practices and tools, to improve the teams ability to execute and meet their goals.
  • Leverage current industry best-practice tools, such as MS Project, Smartsheet, Planisware, etc., to develop and drive integrated project plans, aligning project tactics with project strategy
  • Manage projects within established scope, schedule and budget while exceeding IPM project management standards
  • Participate and if need be drive discussions, and develop and document  high-level strategies for accomplishing specific project objectives
  • Establish, maintain, guide and lead high performance project teams, serving as the project advocate within the client organization
  
DESIRED SKILLS AND EXPERIENCE 
The successful candidate for this position should have the following skills and experience: 
  • A Bachelor’s degree in a science or engineering discipline or relatable field. Advanced degrees in science, engineering or business are a plus.
  • 6-10 years of industry experience in the pharmaceutical industry.
  • 3+ years of project management experience related to one or more of IPM’s business offerings:
    • Within product development and management across the full product life cycle:  pre-clinical research and development; clinical development; regulatory submissions and compliance; commercialization; product management; quality assurance and control
    • Knowledge and application of a disciplined project management process (Six Sigma and Project Management Professional certifications are a plus)
    • Exceptional interpersonal and leadership skills to effectively communicate and build relationships with a broad spectrum of audiences at all organizational levels
    • Demonstrated ability to adapt to new situations and learn quickly.
WHY IPM 
  • Engaging culture:  IPM has a caring, nurturing culture with a transparent communication approach and culture-building and team-building events, both regional and company-wide.
  • Inclusion:  Diversity, Equity and Inclusion have always been a part of our culture; we are a company that treats everyone with respect and dignity.  Everyone has a voice and is heard.
  • Professional development:  We ensure you reach your professional aspirations by providing you with training and development opportunities.  We’ll create the bandwidth you need to further your career at IPM.  You are IPM’s future – we only promote from within.
  • Diverse projects:  We lead a wide variety of projects and provide significant exposure to many clients and project types.
  • Collaborative work environment:  We have a well-structured system to provide support from managers, internal teams, and our Centers of Excellence (CoE).  Our CoEs serve as a resource for specific service and industry knowledge, tools and best practices.
  • Comprehensive compensation and benefits program:  including 100% employer-paid health for employees and 80% paid health for dependents; 401(k)matching, performance bonus, relocation assistance, tuition reimbursement, paid vacation, holiday, personal and sick time, among many others; salary range is $120,000 - $140,000 dependent on experience.
  • Philanthropy:  We are devoted to the communities we serve and actively promote employee involvement in community improvement projects.  We’ve created “Project Mercy” to channel our philanthropic efforts every quarter.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, and market / business considerations. 

IPM is an equal opportunity employer.  We are committed to provide equal employment opportunities to all employees and applicants for employment. 
 
IPM’s hybrid work environment requires a minimum of three days in the office. The specific days are flexible and may vary depending on project schedules and meetings. On-site locations may also vary. In addition, we follow our clients’ guidance on on-site requirements, so the minimum number of days in the office may increase depending on the client and project assignment.