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Biotechnology Project Manager Jobs in Rhode Island

Strategic Sourcing Manager

Providence, RI ยท On-site

$130K - $168K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...

Director of Facilities

Cumberland, RI ยท On-site

$180K - $205K/yr

Neurotech Pharmaceuticals, Inc. is a private biotech company located in Cumberland, RI and Needham ... Read, redline, and manage engineering drawings and equipment files (P&IDs). * Provide project ...

New

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Demonstrated project management and presentation skills, and proven ability to manage priorities ...

New

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Demonstrated project management and presentation skills, and proven ability to manage priorities ...

New

Finance Director, CDMO Operations

Coventry, RI ยท On-site

$180K - $240K/yr

We're proud of the impact we make and just last year, we supported 887 discovery projects , 1,100 ... Manage vendor setup and change processes ensuring adherence to company controls and procedures

It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 ... Able to demonstrate project management skills and presentation skills * Ability to understand ...

It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 ... Able to demonstrate project management skills and presentation skills * Ability to understand ...

Showing results 21-40

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:

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.

Manager QA - Nights - West Greenwich RI

Veteran Jobs - 2023 Mar 01 - Veterans Resources

West Greenwich, RI โ€ข On-site

Other

Posted 19 hours ago

Posted today


Job description

ย 
ATTENTION MILITARY AFFILIATED JOB SEEKERSย - Our organization works with partner companies to source qualified talent for their open roles. The following position is available toย Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is On-Site at the location detailed in the job post.
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Manager QA - Nights
What you will do
Let's do this. Let's change the world. In this vital role you will hire, train, develop, and manage Quality Assurance professionals to successfully deliver on role to support GMP Manufacturing and to manage change in an effective, efficient and compliant manner.
This individual will be responsible for overseeing our Night shift Quality Assurance teams, and the schedule will be M-F 6pm - 2:30am.
Additional Responsibilities:
Independently determine approach to managing daily operations; guided by general policies and management guidance
Develop or contribute to the development of procedures and standards by which others will operate.
Interpret and execute standards and procedures directly affecting work activities
Develops and communicates goals and objectives to staff and key partners
Monitor goal performance and coordinate action for improvement of shift and overall PQA performance by championing department OPEX efforts. Assist project teams in establishing priorities, project timelines and in securing resources.
Actively represent Quality Assurance on incident triage teams or support efforts by providing guidance and/or technical leadership
Partner with internal personnel at various management levels to resolve issues, establish direction, obtain resources, and drive change
Reviewing and approving operational procedures and product manufacturing procedures, approving process validation protocols and reports for manufacturing processes, and approving environmental characterization reports and change control documents.
Approving non-conformances, representing QA on project teams and approving change-over completion controls.
Leading investigations, as well as leading plant and site audits.