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Project Manager Biotech Jobs in Rhode Island (NOW HIRING)

Engineering Manager

West Greenwich, RI ยท On-site

$125 - $169/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project management skills, including planning, prioritization, execution, and stakeholder ...

System Administrator

Cumberland, RI ยท On-site

$130 - $140/hr

... biotech company located in Cumberland, RI and Needham, MA,. Since our inception more than 20 years ... We are seeking a System Administrator to support Facilities management and site operations by ...

System Administrator

Cumberland, RI ยท On-site

$130K - $140K/yr

Neurotech Pharmaceuticals, Inc. is a private biotech company located in Cumberland, RI and Needham ... We are seeking a System Administrator to support Facilities management and site operations by ...

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 41-60

Project Manager Biotech information

See Rhode Island salary details

$21

$45

$74

How much do project manager biotech jobs pay per hour?

As of Sep 7, 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 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 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:

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

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

Infographic showing various Project Manager Biotech job openings in Rhode Island as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $94,194 per year, or $45.3 per hour.

Engineering Manager

Biopharma Careers

West Greenwich, RI โ€ข On-site

$125 - $169/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago


Job description

Career Category

Operations

Job Description

Join Amgenโ€™s Mission of Serving Patients

At Amgen, if you feel like youโ€™re part of something bigger, itโ€™s because you are. Our shared mission, to serve patients living with serious illnesses, drives all that we do.

Since 1980, weโ€™ve helped pioneer the world of biotech in our fight against the worldโ€™s toughest diseases. With our focus on four therapeutic areas โ€“Oncology, Inflammation, General Medicine, and Rare Diseaseโ€“ 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, youโ€™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, youโ€™ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Engineering ManagerWhat you will do

Letโ€™s do this. Letโ€™s change the world. In this vital role you will lead engineering activities that support reliable, compliant, and efficient site operations. You will collaborate with multiple functions on a routine basis in a dynamic environment, including Manufacturing, Quality Assurance, Quality Control, Facilities, Maintenance, Process Development, Process Engineering, Automation, Regulatory Compliance, and other business partners.

With minimal direction, the Manager Engineering is responsible for leading an engineering team that provides technical support, equipment reliability, troubleshooting, project execution, and continuous improvement for site operations. The Manager will be responsible for supervising, coaching, hiring, and developing engineering staff. This role will assist in defining area objectives, identifying improvement opportunities, managing technical priorities, and leading change efforts. The Manager will need to effectively direct their team and deliver on short- and long-term Amgen operational and engineering goals.

Scope of Responsibility
  • Demonstrate technical leadership across engineering systems, equipment, utilities, process support, and/or site infrastructure.
  • Lead engineering support for manufacturing and site operations to ensure reliable, compliant, and efficient performance of equipment and systems.
  • Ensure adherence to Standard Operating Procedures, GMP requirements, engineering standards, safety requirements, change control processes, and applicable regulatory expectations.
  • Troubleshoot equipment issues, system performance concerns, process-support challenges, and operational disruptions in real time.
  • Participate in investigations, audits, and regulatory inspections as an engineering subject matter expert or technical owner.
  • Support deviation investigations, root cause analysis, CAPA development, change controls, technical evaluations, and implementation of corrective and preventive actions.
Leading Strategy Development and Execution
  • Assist in developing and implementing departmental engineering strategy and plans that are aligned with the broader organizational strategy.
  • Anticipate technical, compliance, safety, reliability, and schedule risks and build contingencies to help mitigate impact.
  • Deliver strong business results through identification and implementation of continuous improvements that increase efficiency, equipment reliability, compliance, throughput, and operational resilience.
  • Support lifecycle management of equipment, systems, and infrastructure, including reliability improvements, obsolescence planning, and longโ€‘term asset strategy.
Building a Strong Organizational Alignment
  • Responsible for selection, training, evaluation, staff relations, and development of engineering staff.
  • Interact with management in optimizing organizational structure, technical responsibilities, and resource allocation.
  • Create an environment that fosters accountability, innovation, continuous improvement, learning, technical rigor, and knowledgeโ€‘sharing.
  • Build and develop a diverse, impactful engineering team.
  • Develop strong relationships with staff members and provide open and clear feedback to improve individual and team performance.
  • Build strong partnerships with Manufacturing, Quality, Facilities, Maintenance, Process Engineering, Automation, and other crossโ€‘functional partners to ensure alignment on priorities, risks, and execution plans.

The onboarding phase for this role will last approximately 2โ€“6 weeks, during which time successful incumbents will become familiar with site operations, engineering systems, quality processes, safety expectations, and crossโ€‘functional ways of working. This is a daysโ€‘based role, generally aligned to an administrative schedule, with flexibility required to support business needs, critical operations, shutdowns, investigations, or occasional offโ€‘hours issues as necessary.

What we expect of youBasic Qualifications
  • High school diploma / GED and 12 years of Engineering and/or Operations experience OR
  • Associateโ€™s degree and 10 years of Engineering and/or Operations experience OR
  • Bachelorโ€™s degree and 5 years of Engineering and/or Operations experience OR
  • Masterโ€™s degree and 3 years of Engineering and/or Operations experience OR
  • Doctorate degree

In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced above.

Preferred Qualifications
  • Bachelorโ€™s degree in Engineering, Life Sciences, or a related technical discipline.
  • Knowledge and experience within a cGMP or other highly regulated environment, including a basic understanding of technical elements across engineering, equipment systems, automation, facilities/utilities, biological or chemical processing, and/or operational support.
  • Experience leading engineering, maintenance, reliability, technical operations, automation, facilities, or process-support teams.
  • Strong leadership and teamโ€‘building skills, including coaching, mentoring, counseling, and developing technical talent.
  • Experience improving staff capability, team performance, technical execution, and organizational effectiveness.
  • Experience with performance management, including performance reviews and development planning.
  • Strong conflict resolution skills.
  • Strong analytical problemโ€‘solving skills, including root cause analysis and riskโ€‘based decisionโ€‘making.
  • Project management skills, including planning, prioritization, execution, and stakeholder communication.
  • Understanding of regulatory requirements and expectations in a GMP or highly regulated environment.
  • Ability to be flexible, manage change, and lead teams through ambiguity.
  • Excellent verbal and written communication skills, including the ability to communicate technical topics clearly to technical and nonโ€‘technical audiences.
  • Excellent computer skills with Microsoft Office and experience with systems such as EBR/MES, DeltaV, CMMS, electronic quality systems, or other engineering, automation, maintenance, or quality platforms.
  • Experience with change control, deviation investigations, CAPA, equipment qualification, maintenance strategy, reliability engineering, or continuous improvement methodologies.
What you can expect from us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and wellโ€‘being. From our competitive benefits to our collaborative culture, weโ€™ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a salesโ€‘based incentive plan
  • Stockโ€‘based longโ€‘term incentives
  • Awardโ€‘winning timeโ€‘off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

Equal Opportunity

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

Salary Range

125,062.20USD -169,201.80USD

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