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Project Manager Biotech Jobs in Rhode Island (NOW HIRING)

Sr. Manager, QC-API Manufacturing

Coventry, RI ยท On-site

$120K - $150K/yr

... biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 ... We're proud of the impact we make and just last year, we supported over 780 discovery projects , 1 ...

... biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 ... We're proud of the impact we make and just last year, we supported over 780 discovery projects , 1 ...

This role is pivotal for managing the logistics of an R&D leadership team in a growing biotech firm ... Ability to lead in a support function to the assigned project. * Travel required The statements in ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Actively participate in Capital Project Environmental assessments and design process. * Apply a ...

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Project Manager Biotech information

See Rhode Island salary details

$21

$45

$74

How much do project manager biotech jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for project manager biotech in Rhode Island is $45.29, according to ZipRecruiter salary data. Most workers in this role earn between $39.33 and $49.66 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, and why are they important?

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 are popular job titles related to Project Manager Biotech jobs in Rhode Island? For Project Manager Biotech jobs in Rhode Island, the most frequently searched job titles are:

Project Manager - Process Mechanical Construction

Hart Companies

Cumberland, RI โ€ข On-site

Full-time

Posted 8 days ago


Job description

U.S. Citizen, U.S. Person, or Immigration Status Requirements:
All candidates must be authorized to work in the U.S. without the companyโ€™s immigration sponsorship now or in the future. The company will not offer immigration sponsorship for this position. The company will not seek an export authorization for this role.
A family-owned engineering and construction firm founded in 1941, Hart Companies provides integrated Engineering, Architectural, Construction, and Passivation services to highly regulated and technically demanding industries. With a workforce of over 200 employees, we deliver projects ranging from targeted facility upgrades to complex programs exceeding $100M for clients across the United States.
Rooted in values of honesty, quality, and competence, Hart brings deep technical expertise, a people-first culture, and a client-focused team approach to every projectโ€”delivering safe, high-quality solutions that create lasting value for our clients, our communities, and our employees.
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The Process Mechanical Construction Project Manager (PM) will lead the execution of process pipingโ€“focused mechanical construction projects, working closely with an experienced Project Executive. This role is ideal for someone with a strong background in high-purity/hygienic piping and equipment, particularly within the pharmaceutical, biotechnology, or microelectronics industries.

Youโ€™ll own the full project lifecycleโ€”from estimating through closeoutโ€”driving results across scheduling, procurement, cost control, quality, and safety. Success in this role requires a detail-oriented, analytical mindset, along with the ability to communicate effectively with clients, field teams, subcontractors, and senior leadership.


KEY RESPONSIBILITIES

Estimating
Review drawings and specifications to develop accurate bids covering materials, labor, equipment, overhead, and subcontractor costs. Apply a strong understanding of process mechanical systems and technical requirements.

Scheduling
Develop and manage project schedules aligned with client expectations and construction sequencing. Track progress using MS Project and collaborate with field teams to adjust timelines in real time.

Procurement
Execute and manage purchase orders and subcontracts. Evaluate vendor and subcontractor proposals, ensure contract compliance, and coordinate timely delivery of materials and equipment.

Labor Coordination
Partner with foremen to align on schedule, safety, and cost expectations. Plan and forecast manpower needs to support efficient project execution.

Quality Control (QA/QC)
Oversee quality processes, including weld procedures, inspections, and documentation. Ensure all materials and installations meet project specifications and industry standards.

Change Management
Identify and manage scope changes, including pricing, documentation, and client communication, through established change control processes.

Safety Compliance
Promote and enforce OSHA standards, corporate safety policies, and client EHS requirements. Conduct field reviews and reinforce a strong safety culture.

Reporting
Provide clear, consistent updates on schedule, costs, risks, and overall project performance.


ESSENTIAL QUALIFICATIONS

Education
Bachelorโ€™s degree in Construction Management, Engineering, Architecture, or a related field preferred. Equivalent trade experience or technical training will be considered.

Experience
5+ years of project management experience in high-purity/hygienic piping and equipment within pharma, biotech, or microelectronics environments.

Skills

  • Strong communication, leadership, and negotiation abilities
  • Proven problem-solving and decision-making skills
  • Solid understanding of process mechanical systems and construction practices

WORK ENVIRONMENT
  • Combination of office and active construction site work
  • Travel to project sites throughout New England as needed

Hart Companies is committed to building a diverse and inclusive workplace and is proud to be an equal opportunity employer.

All offers are contingent upon successful completion of a background check, which may include a driving record review, and drug screening per client request.

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