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Biotechnology Project Manager Jobs in Boston, MA

Seeking an experienced Project Manager to act as an owner's representative on large, complex ... the biotech industry with proven knowledge of current Good Manufacturing Procedures (cGMP ...

Sr Project Manager

Cambridge, MA · On-site

$143K - $143K/yr

... managing IT projects in Biotech/Pharma involving processes and systems is required! Responsibilities: Leads moderately complex projects from project initiation to implementation. Facilitates the ...

Electrical Project Manager

Boston, MA · On-site

$140K - $190K/yr

Project Manager - Commercial Electrical Construction Location: Greater Boston, MA Salary: $140,000 ... Life Science / Biotechnology. * Commercial Office. * Higher Education / Institutional.

New

The Project Manager II operates independently within PMO standards, defines scope and schedule, and ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

The Project Manager II operates independently within PMO standards, defines scope and schedule, and ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

... upstream and downstream biotech equipment, single use disposable, or aseptic fill finish ... The CAI project manager typically reports to either a client manager or an area manager.

Manage overall C&Q scope, budget, schedule, resource planning, and project risks. * Serve as the ... regulated pharmaceutical, biotechnology, cell and gene therapy, or medical device projects.

Showing results 21-40

Biotechnology Project Manager information

See Boston, MA salary details

$23

$50

$83

How much do biotechnology project manager jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for biotechnology project manager in Boston, MA is $50.24, according to ZipRecruiter salary data. Most workers in this role earn between $43.61 and $55.10 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 job categories do people searching Biotechnology Project Manager jobs in Boston, MA look for?

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

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

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

Infographic showing various Biotechnology Project Manager job openings in Boston, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $104,489 per year, or $50.2 per hour.

Full-time

Medical, Dental, Vision, Life, PTO

Posted 14 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

63rd of 86 rated pharmaceutical


Job description

Project Manager

Catalent's Chelsea, Massachusetts site-often referred to as the Boston location-is a global Center of Excellence for spray dry dispersion (SDD) and dry powder inhaler (DPI) capsule manufacturing and packaging, supporting inhalation drug products from clinical development through commercial launch. Located at 190 Everett Avenue, the approximately 96,000squarefoot GMP facility features ISO 8 production suites, highpotency containment capabilities, and advanced spray drying equipment, including multiple largescale GMP spray dryers. The site offers integrated services such as powder processing, capsule filling, blister packaging, and onsite quality control and analytical testing, with capacity to produce up to 100 million capsules annually. Strategically positioned just minutes from Boston Logan International Airport and within the Greater Boston life sciences hub, the Chelsea site plays a critical role in Catalent's global inhalation network and regulatorycompliant manufacturing operations.

Position Summary

The Project Management function is responsible for managing the non-technical aspects of projects at Catalent Boston which include customer projects for the development and manufacturing of inhalation products and oral spray dried powders. This includes ensuring on time and on budget delivery of projects and acting as a focal point between customers and our technical team by using project management methodologies and corporate PMO procedures.

This position is responsible for managing activities for a portfolio of projects through leading analytical development and/or manufacturing project teams (and other project teams as designated). This position is the main point of customer contact for project related activities and involves managing the execution of the customer's requirements as per an agreed upon program of activities. He/she is responsible for overall project knowledge and execution according to the agreed upon deliverables and timeline.

Shift: Monday - Friday, 8:00am to 5:00pm
Location: Chelsea, MA
100% Onsite

The Role

  • Ensure meeting minutes, agendas, timelines, trackers, and other tools are used effectively for customer projects
  • Assist Business Development in maintaining customer relationships and ensuring return business by communicating with customers, coordinating visits, and acting as the customer advocate
  • Develop, coordinate, and track client projects through the entire project life cycle
  • Monitor and report project progress within agreed timelines, ensuring technical and financial goals are met; Consult and advise upper management on project status and report issues that may affect results
  • Evaluate, highlight, and escalate unresolved issues, potential barriers, and resource constraints to the supervisor; Prepare verbal reports and presentations on project progress as needed
  • Coordinate the revision of Standard Operating Procedures, Batch records, and other site-specific documents for clients
  • Follow up to ensure incident reports are closed in a timely manner and notify clients within 24 hours of any incident
  • All other duties as assigned

The Candidate

Minimum Requirements

  • Bachelor's Degree is required; Life sciences discipline is preferred
  • 2+ years of relevant experience is required; preferably in a Contract Research Organization (CRO) or Contract Development and Manufacturing Organization (CDMO) environment
  • Excellent communication, negotiation, and interpersonal skills are required
  • Proficiency using Microsoft Office Excel, Word, PowerPoint, and Microsoft Project
  • Lifting up to 10 lbs. as needed

Preferred Skills & Background

  • Previous pharmaceutical or biotech industry experience is preferred

Pay

The anticipated salary range for this position in MA is $90,000 - $105,000. Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

Why You Should Join Catalent

  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • Competitive paid time off plus 8 paid holidays
  • Community engagement and green initiatives
  • Medical, dental, and vision benefits effective day one of employment
  • Tuition Reimbursement

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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