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

Validation Project Managers

Burlington, MA ยท On-site

$78K - $98K/yr

The responsibilities of the Validation Project Manager include: 1) Manage multiple customer ... biotechnology or pharmaceutical industries. In addition, the employer requires the following: 1) ...

Revit Model Manager

Woburn, MA ยท On-site

$80 - $100/hr

Opportunity for advancement Job Title Revit Model Manager Position Location Greater Boston, MA ... biotechnology, or life sciences project experience is a plus. * Highly organized with excellent ...

Revit Model Manager

Woburn, MA ยท On-site

$35 - $45/hr

Revit Model Manager Position Location: Greater Boston, MA (South of Boston) Approx. Length of ... biotechnology, or life sciences project experience is a plus. * Highly organized with excellent ...

Proven experience in project management, preferably in the pharmaceutical or biotechnology industries. * Strong understanding of engineering principles and their application to pharmaceutical ...

Manager, Business Development

Waltham, MA ยท Hybrid

$125K - $149K/yr

Strong analytical, communication, project management and project leadership skills, as well as an ... A broad business understanding of the pharmaceutical/biotech industry and the ability to coordinate ...

Manager, Business Development

Waltham, MA ยท On-site

$125K - $149K/yr

Strong analytical, communication, project management and project leadership skills, as well as an ... A broad business understanding of the pharmaceutical/biotech industry and the ability to coordinate ...

Project Engineer

Devens, MA ยท On-site

$85K - $100K/yr

... and biotech customers. With deep technical expertise and impressive flexibility, we develop ... Manage projects from initial concept development to mechanical completion and commissioning ...

Showing results 41-60

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:

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.

Validation Project Managers

Merck Group

Burlington, MA โ€ข On-site

$78K - $98K/yr

Full-time

Re-posted 25 days ago


Job description

Work Location: Burlington, Massachusetts
Shift:
Department: LS-PS-PVUB VPM
Recruiter: Ashley Hennessy
This information is for internals only. Please do not share outside of the organization.
NOTICE OF FILING
This notice is posted as the result of the filing of an Application for Alien Labor Certification with the Department of Labor for the job opportunity listed below. Any person may provide documentary evidence bearing on this Labor Certification Application to Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue NW, Room N-5311, Washington, DC 20210.
Position: Validation Project Managers
Employer: EMD Millipore Corporation
400 Summit Drive
Burlington, Massachusetts 01803
Job Site: 400 Summit Drive
Burlington, Massachusetts 01803
Telecommuting: Telecommuting is an option.
Responsibilities:
The responsibilities of the Validation Project Manager include: 1) Manage multiple customer projects - including bacterial retention testing, physical testing (compatibility, product bubble
point/diffusion, and/or Vmax) and extractables and leachables - from order to final report, ensuring successful completion; 2) Develop realistic project plans shared with customers,
monitoring progress and adjusting timelines as necessary; 3) Serve as the liaison between customers and validation service teams to coordinate activities effectively; 4) Communicate
proactively with customers and internal teams through timely updates, meetings, and discussions; 5) Create, update, track, and close projects accurately and in a timely manner; 6) Provide adequate level of technical support for standard services. Help customers define their needs and answering basic questions; 7) Consult with VPMs, laboratory experts, and support teams for necessary project information and assistance; and 8) Assist with standard quotations based on customer needs and regulatory requirements while providing technical support. At least
three days of in-office work per week are required, so the individual must reside in the Burlington, MA area.
Requirements & Qualifications:
The employer requires a bachelor's degree in Biology, Biochemistry, Chemistry or closely related field and at least two years of work experience in any occupation within the biotechnology or pharmaceutical industries. In addition, the employer requires the following: 1) Demonstrated knowledge of extractables and leachable validation gained through at least two years of work experience; 2) Demonstrated knowledge of project management and scheduling tools such as SalesForce, Smartsheet, SharePoint, and Microsoft 360 gained through at least two
years of work experience; 3) Demonstrated knowledge of quality assurance and Good Documentation Practices (OSHA, EHS, ISO9001) gained through at least two years of work
experience; and 4) Demonstrated ability working with root cause analysis gained through at least two years of work experience. All years of experience may be gained concurrently
This position is eligible for EMD Millipore Corporation's Employee Referral Program.
Applicants can send resumes to EMD Millipore Corporation 400 Summit Drive, Burlington, Massachusetts 01803 (Attn: Req#301608) or apply online at https://careers.emdgroup.com
Salary Range: $78,208 to $98,208 per year.
Compensation is based on experience, location, and other factors. We offer generous benefits packages: https://careers.emdgroup.com/us/en/benefits
DATE POSTED: DATE REMOVED:
LOCATION POSTED:
EMPLOYER SIGNATURE:
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.