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

Senior Project Engineer

Jaffrey, NH ยท On-site

$116K - $175K/yr

Manage change control and re-validation to maintain ongoing compliance. * Equipment build ... You have 5 years of professional experience in medical, biotechnology, or Bio-pharmaceutical ...

Principal Project Engineer

Jaffrey, NH ยท On-site

$112K - $168K/yr

At the same time, you might have the opportunity to manage smaller projects from ideation to ... You have 8 years of professional experience in medical, biotechnology, or Bio-pharmaceutical ...

Project Manager Biotech information

See Orange, MA salary details

$21

$45

$75

How much do project manager biotech jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for project manager biotech in Orange, MA is $45.63, according to ZipRecruiter salary data. Most workers in this role earn between $39.62 and $50.05 per hour, depending on experience, location, and employer.

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.

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 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.
What cities near Orange, MA are hiring for Project Manager Biotech jobs? Cities near Orange, MA with the most Project Manager Biotech job openings:
Infographic showing various Project Manager Biotech job openings in Orange, MA as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $94,906 per year, or $45.6 per hour.

Senior Project Engineer

Merck Group

Jaffrey, NH โ€ข On-site

$116K - $175K/yr

Full-time

Medical, Retirement, PTO

Re-posted 15 days ago


Job description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Your role:
As a Senior Project Engineer in the Engineering & Technology Team you are a critical business partner to ensure we will meet our ambitious investment objectives in our Life Science business unit. You will support the preparation and execution of large, strategic investment projects as a technical expert for process engineering. The projects are large (multi-million dollars) and/or of a complex nature. You will support the sites and business stakeholders in developing the technical project scope and ensure seamless implementation of the most efficient, viable technical solution in alignment with internal standards and any binding requirements. At the same time, you might have the opportunity to manage smaller projects from ideation to implementation. You will also contribute to the execution of the LS strategy and strive for technological advancement by fulfilling internal customer requirements with state-of-the-art and sustainable solutions, leveraging the internal technology network across the whole organization.
You will be supporting the North American region. The position is located in Jaffrey, NH USA
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Key Responsibilities
Manage Equipment validation and qualification
    • Manage change control and re-validation to maintain ongoing compliance.
  • Equipment build, commissioning, and start-up
    • Influence equipment design inputs, vendor selection, and build for manufacturability and reliability.
    • Lead FAT/SAT, installation/commissioning, site acceptance testing, and handover to operations.
  • Project governance and planning
    • Develop and maintain WBS, schedules, milestones, and critical-path analyses.
    • Establish vendor evaluation criteria, due diligence, and gating processes.
  • Risk, safety, and compliance
    • Conduct hazard analyses, FMEA; ensure alignment with internal standards and regulatory requirements.
  • Documentation and communication
  • Create and Maintain standardized templates for charters, business cases, and risk registers
    • Provide clear, factual reporting to stakeholders and governance bodies.

Who you are:
Minimum Qualifications:
  • BS or MS in Engineering (Mechanical Engineering preferred)
  • You have 5 years of professional experience in medical, biotechnology, or Bio-pharmaceutical manufacturing environment is highly preferred.

Preferred Qualifications:
  • PMP certification preferred, not required.
  • Fluent in English with excellent communication skills and have a profound knowledge of quality regulations.
  • Ability to analyze situations and systems to develop or identify optimized solutions in line with project scope, time, and cost.
  • History of successfully implemented equipment or systems along the whole value chain from design, build installation and start-up.
  • Prior experience in medical, biotechnology or similar field preferred.
  • Knowledge of manufacturing concepts and GMP.
  • Must be a strong communicator, self-starter and work with minimal supervision.
  • Ability to prioritize and work on multiple projects.
  • Enthusiastic, cooperative, and positive behavior
  • Must have significant skills and experience in project management and ideally a history of successfully executed smaller technical investment projects (0.5M$-10M$) as a project lead (production machine equipment preferred).
  • Ability to work effectively and have demonstrated documentation skills.
  • Inclusive and can identify required resources, internal or external experts and stakeholders.
  • Domestic travel up to 30%

Pay Range for this position: $116,700-$175,100
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!