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Biotechnology Project Manager Jobs in Rhode Island

Pharmaron

Senior Project Engineer

Coventry, RI · On-site

$120K - $140K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Project Management: * Lead capital projects from equipment upgrades to facility expansions.

New

Pharmaron

Senior Project Engineer

Coventry, RI

$120K - $140K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Project Management: * Lead capital projects from equipment upgrades to facility expansions.

New

Aequor

Supply Chain Manager

West Greenwich, RI · On-site +1

Fully Remote - US-Based, Any time zone Ideal Candidate: 5+ YOE in GMP warehousing is a must have, strong preference for Pharma or Biotech experience, script testing, and basic project management ...

JLL

Senior Facilities Manager

West Greenwich, RI · On-site

Coordinate and oversee capital improvement projects, working with engineering teams, contractors ... pharmaceutical, biotech, or similarly regulated environments * Demonstrated expertise in GMP ...

Amgen

Manager QA - Nights

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Approving non-conformances, representing QA on project teams and approving change-over completion ...

Amgen, Inc.

Manager QA - Nights

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Approving non-conformances, representing QA on project teams and approving change-over completion ...

Amgen, Inc.

Validation Engineer

West Greenwich, RI · On-site

... Management organization at Amgen Rhode Island (ARI), a large-scale mammalian cell biotech ... Serve as the validation technical expert during project planning, equipment implementation, design ...

Amgen Inc. (IR)

Validation Engineer

West Greenwich, RI · On-site

$86 - $116/hr

... Management organization at Amgen Rhode Island (ARI), a large-scale mammalian cell biotech ... Serve as the validation technical expert during project planning, equipment implementation, design ...

New

Amgen SA

Validation Engineer

West Greenwich, RI · On-site

$90 - $130/hr

... Management organization at Amgen Rhode Island (ARI), a large-scale mammalian cell biotech ... Serve as the validation technical expert during project planning, equipment implementation, design ...

Posted today

Amgen

Validation Engineer

West Greenwich, RI · On-site

... Management organization at Amgen Rhode Island (ARI), a large-scale mammalian cell biotech ... Serve as the validation technical expert during project planning, equipment implementation, design ...

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All JobsBiotechnology Project JobsBiotechnology Project Manager JobsBiotechnology Project Manager Jobs in Rhode Island

Biotechnology Project Manager information

See Rhode Island salary details

$21

$45

$74

How much do biotechnology project manager jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for biotechnology project manager 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 does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Biotechnology Project Manager jobs in Rhode Island?

For Biotechnology Project Manager jobs in Rhode Island, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Rhode Island look for?

The top searched job categories for Biotechnology Project Manager jobs in Rhode Island are:

What cities in Rhode Island are hiring for Biotechnology Project Manager jobs?

Cities in Rhode Island with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Rhode Island as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $94,194 per year, or $45.3 per hour.

Senior Project Engineer

Pharmaron

Coventry, RI • On-site

$120K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Job description

Position: Senior Project Engineer
Salary Range: $120K-$140K
Location: Coventry, RI
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
What You'll Do
The Senior Project Engineer will lead the planning, execution, and delivery of capital projects supporting small-molecule pharmaceutical manufacturing and research operations. This role will manage projects from initial concept through commissioning, qualification, and final handover while ensuring compliance with current Good Manufacturing Practices (cGMP), regulatory requirements, Environmental Health and Safety (EHS) standards, and site engineering standards.
As a technical leader and project manager, the Senior Project Engineer will oversee facility, utility, process equipment, and infrastructure projects. Success in this role requires strong cross-functional collaboration with Maintenance, Manufacturing, Quality Assurance, EHS, Supply Chain, and external engineering and construction partners to deliver projects safely, on schedule, and within budget.
Project Management:
  • Lead capital projects from equipment upgrades to facility expansions.
  • Develop scopes, budgets, schedules, and execution plans.
  • Manage multiple projects while tracking scope, cost, schedule, quality, and risk.
  • Communicate project status and maintain required change-control documentation.
  • Engineering & Technical Leadership
  • Lead project design, cost estimates, technical studies, and feasibility assessments.
  • Develop and review engineering packages, specifications, PFDs, P&IDs, layouts, and drawings.
  • Support equipment procurement and ensure solutions meet manufacturing, quality, safety, and regulatory requirements.

Capital Project Execution:
  • Coordinate engineering consultants, contractors, and equipment vendors.
  • Oversee construction, design reviews, FATs/SATs, commissioning, and qualification.
  • Support system integration, troubleshooting, and start-up activities.
  • Safety & Environmental Compliance
  • Ensure projects meet EHS, OSHA, PSM, and site safety requirements.
  • Participate in HAZOPs, risk assessments, and process safety reviews.
  • Promote a strong safety culture and support contractor safety training and field activities.

What We're Looking For:
Required Education: Bachelor's degree in Chemical Engineering, Mechanical Engineering, or a related engineering discipline.
Required Experience & Qualifications:
  • 7+ years of relevant experience in capital project design and execution within pharmaceutical ingredients, specialty chemicals, fine chemicals, or a related manufacturing environment.
  • Experience managing capital projects from concept through design, construction, commissioning, and handover.
  • Familiarity with a broad range of manufacturing unit operations, utility systems, and associated equipment.
  • Demonstrated ability to lead cross-functional teams and effectively collaborate with internal stakeholders, contractors, consultants, and vendors.
  • Strong project management, organizational, communication, and problem-solving skills.
  • Familiarity with OSHA Process Safety Management (PSM) requirements and other applicable industry codes and regulations.

Preferred Qualifications:
  • Professional Engineer (PE) license.
  • Experience in a cGMP manufacturing environment.
  • Experience spanning both project engineering and process engineering.
  • Knowledge of automation and control systems, including PLC, DCS, SCADA, BMS, or similar platforms.
  • Familiarity with cGMP requirements and FDA regulations.
  • Experience leading complex, multidisciplinary capital projects in a regulated manufacturing environment.

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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