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Project Manager Biotech Jobs in Raleigh, NC (NOW HIRING)

Bachelor's degree in chemistry, Life Sciences, or a related field with 2-4 years of relevant experience in project management within the pharmaceutical, biotech, or CDMO industry. * PMP certification ...

Bachelor's degree in chemistry, Life Sciences, or a related field with 2-4 years of relevant experience in project management within the pharmaceutical, biotech, or CDMO industry. * PMP certification ...

Bachelor's degree in chemistry, Life Sciences, or a related field with 2-4 years of relevant experience in project management within the pharmaceutical, biotech, or CDMO industry. * PMP certification ...

... biotech and medical device industries. We do this across six continents, and we'll do it for you ... Works in the role of a project manager on assigned project(s), which may range from single service ...

... biotech and medical device industries. We do this across six continents, and we'll do it for you ... Works in the role of a project manager on assigned project(s), which may range from single service ...

The successful candidate must have a strong design discipline background along with experience managing architectural and engineering/design projects in the biotech, pharmaceutical, or nutraceutical ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Engineering Project Manager Duties: Applies working knowledge of process equipment, material flow ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Engineering Project Manager Duties: Applies working knowledge of process equipment, material flow ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Engineering Project Manager Duties: Applies working knowledge of process equipment, material flow ...

New

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Engineering Project Manager Duties: Applies working knowledge of process equipment, material flow ...

Showing results 21-40

Project Manager Biotech information

See Raleigh, NC salary details

$21

$44

$74

How much do project manager biotech jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for project manager biotech in Raleigh, NC is $44.95, according to ZipRecruiter salary data. Most workers in this role earn between $39.04 and $49.33 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 Raleigh, NC?

For Project Manager Biotech jobs in Raleigh, NC, the most frequently searched job titles are:

What cities near Raleigh, NC are hiring for Project Manager Biotech jobs?

Cities near Raleigh, NC with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Raleigh, NC as of August 2026, with employment types broken down into 88% Full Time, 10% Part Time, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $93,499 per year, or $45 per hour.

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Raleigh, NC • On-site

MMR Consulting
51 - 200 employees

Other

Re-posted 18 days ago


Job description

Previous Pharmaceutical/Biotech experience is mandatory for this role.

MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process, Automation, Facilities and Equipment CQV.

MMR Consulting has offices in Canada, USA, and Australia.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in project management, commissioning and qualification, of equipment, systems and facilities.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work will require working out of client’s facilities.

The work will require working out of the client’s facilities in Raleigh, North Carolina.

Responsibilities
  • Provide technical guidance into the assessments, design, project management, commissioning and start-up of equipment and facilities, for upgrades, renovations and expansions of client facilities and processes.
  • Lead or support project execution from feasibility through to project completion/handover, including all project stages such as:
    • Feasibility Assessments
    • Concept Design, Basic Design, Detailed Design
    • Procurement
    • Construction / Installation
    • Project Controls - Monitoring
    • Commissioning & Qualification
  • Prepare business cases, with project purpose, risks, budget, schedule, resource requirements.
  • Manage other design firms, equipment vendors, construction firms and internal / external stakeholders as required to execute projects.
  • Manage Capital Projects
  • Review technical documentation such as P&IDs, specifications, layouts, manuals, datasheets.
  • Integrate safety into the design and execution of all projects (HAZOP reviews, PHSRs, design reviews with EHS representatives).
  • Prepare/review automation sequences, as required for Process Automation.
  • Engage and coordinate with other other cross-functional departments (Process, automation, building / facilities, procurement, construction management, commissioning, qualification & validation, manufacturing operations, EHS, quality & compliance).
  • Facilitate project management tools throughout the execution of projects, such as procurement tracking, vendor management, meeting minutes / action lists, risk register log, schedule updates, project updates.
  • Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
  • Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
  • Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification & validation phases.
  • You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
  • Visit construction and installation sites, wear necessary safety PPE.
  • Supervise contractors during critical installations of process equipment and associated utilities.
  • Other duties as assigned by client, and/or MMR, based on workload and project requirements.
  • As this position requires working on client sites, you will need to comply with the client’s safety rules including mandatory vaccination policies for COVID-19, where applicable.
Qualifications
  • 10+ years of experience in the biotech industry in project management of various equipment and facilities within the pharmaceutical/biotech industry, with knowledge of requirements for a cGMP operation.
  • Previous PM capital projects experience is required.
  • Previous Greenfield projects experience is required.
  • Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.
  • Possess mentorship skills, to coach and develop junior and intermediate employees.
  • Basic knowledge of AutoCAD.
  • Degree, preferably in Mechanical, Chemical, Electrical or other industry related discipline.
  • Certification in Project Management would be an asset.
  • Travel may be required on occasion. Ability to travel to the US would be an asset.
Equal Employment Opportunity and Reasonable Accommodations

MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

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