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Project Manager Biotech Jobs in Windham, NH (NOW HIRING)

RQMIS Inc

Be Seen First

Clinical Trials Project Manager

Amesbury, MA · On-site

RQMIS Inc. is a fast growing, medical device/biotechnology consultancy with a focus on regulatory ... The Clinical Trials Project Manager will: * Develop/implement/ manage all aspects of clinical ...

Bristol-Myers Squibb

Capital Project Manager

Devens, MA · On-site

$110K - $133K/yr

A minimum of 6 years of experience in conceptual development, project management, planning and scheduling on capital projects, including experience in the Biotech or related industry. Knowledge and ...

Bristol Myers Squibb

Capital Project Manager

Devens, MA · On-site

$110K - $133K/yr

A minimum of 6 years of experience in conceptual development, project management, planning and scheduling on capital projects, including experience in the Biotech or related industry. * Knowledge and ...

Veranova L P

Senior Project Manager

Devens, MA · On-site

Senior Project Manager Discover Veranova: At Veranova, we believe people are our most important ... and biotech customers. With deep technical expertise and impressive flexibility, we develop ...

Repligen

R&D Project Manager II

Waltham, MA

$110K - $135K/yr

Experience managing projects in bioprocessing, biotechnology, or a related life sciences field is a plus. Our mission is to inspire advances in bioprocessing as a trusted partner in the production of ...

Repligen Corporation

R&D Project Manager II

Waltham, MA · On-site

$110K - $135K/yr

Experience managing projects in bioprocessing, biotechnology, or a related life sciences field is a plus. Our mission is to inspire advances in bioprocessing as a trusted partner in the production of ...

Repligen

R&D Project Manager II

Waltham, MA

$110K - $135K/yr

Experience managing projects in bioprocessing, biotechnology, or a related life sciences field. * Demonstrated track record of successful project execution * Ability to work effectively across ...

Integrated Resources INC

Project Engineer

Waltham, MA · On-site

Project Management Experience * Engineering on the manufacturing side within Pharma/Biotech experience If they do not have pharma/biotech they need 5+ years engineering experience Must be GMP ...

PM Group

Senior Project Director

Burlington, MA

We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors ... Mentor the Project Management team * Focus on building and retaining a key core team through ...

PM Group

Senior Project Director

Burlington, MA · On-site

We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors ... Mentor the Project Management team * Focus on building and retaining a key core team through ...

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Showing results 21-40

All JobsProject Biotech JobsProject Manager Biotech JobsProject Manager Biotech Jobs in Windham, NH

Project Manager Biotech information

See Windham, NH salary details

$22

$48

$79

How much do project manager biotech jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for project manager biotech in Windham, NH is $48.28, according to ZipRecruiter salary data. Most workers in this role earn between $41.92 and $52.93 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 job categories do people searching Project Manager Biotech jobs in Windham, NH look for?

The top searched job categories for Project Manager Biotech jobs in Windham, NH are:

What cities near Windham, NH are hiring for Project Manager Biotech jobs?

Cities near Windham, NH with the most Project Manager Biotech job openings:

Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Windham, NH as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $100,415 per year, or $48.3 per hour.

Clinical Trials Project Manager

RQMIS Inc

Amesbury, MA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago

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Job description

RQMIS Inc. is a fast growing, medical device/biotechnology consultancy with a focus on regulatory strategy/submissions, clinical study design/management and quality systems design/compliance/auditing.

OVERALL RESPONSIBILITIES:

The Clinical Trials Project Manager will:

  • Develop/implement/ manage all aspects of clinical trials in domestic and international countries for our clients.
  • Provide training to clients and internal staff on such areas as clinical trial management, good clinical practices (GCPs), FDA Biomonitoring, CRF design, clinical report writing, Clinical Study Monitoring, etc.

POSITION DUTIES & RESPONSIBILITIES:

  • Manage all aspects of clinical projects
  • Provide training to clients and internal staff
  • Write departmental procedures and assist in training efforts
  • Participate in special projects as needed
  • Travel required (up to 30 to 50%)
  • Other duties as assigned

EDUCATION & PROFESSIONAL EXPERIENCE:

  • Bachelor’s degree in clinical/science field, or similar work experience
  • 5 to 7 years experience in medical device clinical trials
  • Previous supervisory or team leadership experience
  • Knowledge of domestic/international medical device regulations
  • Strong attention to detail
  • Strong computer skills, including word processing, spreadsheet and data programs
  • Good oral and written communication skills
  • Good leadership skills
  • Ability to manage several tasks simultaneously while continuously assessing company and/or departmental priorities

Company Description

RQMIS Inc is located north of Boston Massachusetts area is a fast growing medical device/ biotechnology consultancy with focused in three principle areas, regulatory strategy/submissions, clinical study design/management and quality systems design/compliance. RQMIS Inc has been providing companies with strategic guidance on how to effectively navigate the FDA, UK and EU regulations for over 25 years in around the world.