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Project Manager Biotech Jobs in Brighton, MA (NOW HIRING)

QUANTERIX CORP

Project Manager

Bedford, MA · On-site

$100K - $120K/yr

Project Manager, Custom Assay Development Bedford, MA Quanterix is a global leader in ultra ... biotechnology, diagnostic, CRO, or life sciences environment and possess strong communication ...

Quanterix

Project Manager

Bedford, MA · On-site

$100K - $120K/yr

Project Manager, Custom Assay DevelopmentBedford, MAQuanterix is a global leader in ultra-sensitive ... biotechnology, diagnostic, CRO, or life sciences environment and possess strong communication ...

Cognito Therapeutics

Project Manager

Cambridge, MA · On-site +1

Project Manager, Office of the CEO, Cognito Therapeutics, Inc. Location: Boston, or Remote USA ... Experience in biotech, medical device, pharmaceutical, healthcare technology, or another high ...

Integrated Resources INC

Project Manager

Lexington, MA · On-site

Qualifications Bachelor's degree required At least 5-7 years' experience in a project manager role Familiarity of Pharmaceutical / Biotech Global Medical Affairs organization and / or Research and ...

Catalent Pharma Solutions

Project Manager

Chelsea, MA · On-site

Project Manager Catalent's Chelsea, Massachusetts site-often referred to as the Boston location-is ... Previous pharmaceutical or biotech industry experience is preferred Pay The anticipated salary ...

Catalent, Inc.

Project Manager

Chelsea, MA · On-site

Project Manager Catalent's Chelsea, Massachusetts site-often referred to as the Boston location-is ... Previous pharmaceutical or biotech industry experience is preferred Pay The anticipated salary ...

WhiteCap Search

CMC Project Manager

Cambridge, MA · On-site

Familiarity with pharmaceutical or biotechnology development and manufacturing processes. * Experience with project planning, timeline management, risk tracking, stakeholder communication, and ...

Syner-G

Project Manager

Marlborough, 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 ...

Integrated Resources INC

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 ...

Allegiance Group

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.

Nova Biomedical

Project Manager II

Waltham, MA

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 ...

Nova Biomedical

Project Manager II

Waltham, MA · On-site

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 ...

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Project Manager Biotech information

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How much do project manager biotech jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for project manager biotech in Brighton, MA is $50.40, according to ZipRecruiter salary data. Most workers in this role earn between $43.75 and $55.29 per hour, depending on experience, location, and employer.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What are popular job titles related to Project Manager Biotech jobs in Brighton, MA?

For Project Manager Biotech jobs in Brighton, MA, the most frequently searched job titles are:

What job categories do people searching Project Manager Biotech jobs in Brighton, MA look for?

The top searched job categories for Project Manager Biotech jobs in Brighton, MA are:

What cities near Brighton, MA are hiring for Project Manager Biotech jobs?

Cities near Brighton, MA with the most Project Manager Biotech job openings:

Project Manager Biotech jobs near you

CMC Project Leader

HONGENE BIOTECH CORPORATION

Cambridge, MA • On-site

$140K - $190K/yr

Full-time

Re-posted 20 days ago

Job description

Job Title

Associate Director / Senior Manager, CMC Project Management

Location

Boston area preferred (or ability to commute regularly)

Company Overview

Hongene Biotech is a global leader in nucleic acid manufacturing, supporting RNA therapeutics, mRNA vaccines, and molecular diagnostics. With a vertically integrated platform from raw materials to CDMO services, we enable our partners to accelerate development with efficiency and quality.

Position Overview

This role will report directly to the VP, Global Head of CMC & Regulatory and is critical in strengthening Hongene’s project management capabilities for its oligonucleotide contract manufacturing services.

Level and title will be determined based on experience. We are primarily targeting Senior Manager to Associate Director level. Exceptional candidates may be considered at Director level.

The Primary Job Responsibilities

1) Drive project management efforts associated with CMC activities to support oligonucleotide contract manufacturing projects at Hongene Biotech.

2) Support Head of CMC and Oligonucleotide team in developing and executing development and manufacturing strategy and tactical executional plans.

3) Bridge communication between Clients and the internal teams in support of multiple contract manufacturing projects for different clients, including participation in technical calls, tracking of action items and facilitating rapid decision making within the team to drive programs forward.

4) Coordination with AD/PD, manufacture, quality and BD team to build, and manage global clients’ project timelines, work with BD to generating RFP proposals and evaluate necessary resources and ensure RFP proposals are aligned with overall strategy and cost estimation. Proactively identify potential risks, resourcing constraints and conflicts that could impact project timelines; collaborate with the AD/PD, manufacturing, QA/QC teams to develop appropriate solutions.

5) Support projects with strategic partners in US.

The candidate must have strong communication skills and be capable of strategically communicating with internal and external stakeholders, as well as effectively communicating across functions and fluent speaking both English and Mandarin. Finally, the candidate must be comfortable with, and thrive in, a fast-paced entrepreneurial environment.

Minimal Requirements

• B.S or M.S in Pharmaceutical Science, Chemistry, Biochemistry, or related scientific discipline with 8+ years of applicable experience in the biotechnology or pharmaceutical industry.

• Demonstrated proficiency in the discipline of project management. Experience with operating in a GMP environment and working in cross functional environments. Demonstrated ability to exercise independent judgement and strategic thinking.

• Strong interpersonal skills and experience of managing cross-function projects.

• Ability to thrive in a fast-paced, hands-on research and development environment.

• Adept at building strong relationships and collaborating with colleagues at all levels.

• Ability to discern paths forward within ambiguous environments.

• Excellent verbal, written, and presentation skills for communication with internal and external customers is essential.

Preferred Qualifications

• Minimum of 5 years’ experience in project or program management at a biotechnology or pharmaceutical company with direct involvement in the CMC area

• Experience with project management tools (e.g. MS Project, Smartsheet, Clarizen) and collaboration tools (BOX, SharePoint, MS Teams)

• Understanding of the different phases of drug development and cGMP requirements

• Experience in small molecules, oligonucleotides, or biologic drug development

• Located in US EST time zone