1

Biotech Project Management 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 ...

Project Manager, Services

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology company. Founded in 2012, EpiCypher ® was created in response to the growing demand ... Candidate will leverage skills in project management and knowledge of molecular biology to support ...

Project Executive (Life Sciences)

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biotechnology market sectors. This role requires a strong focus on stakeholder management, the ... Oversee and direct construction projects from conception to completion. * Work with customer ...

Project Executive (Life Sciences)

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biotechnology market sectors. This role requires a strong focus on stakeholder management, the ... Oversee and direct construction projects from conception to completion. * Work with customer ...

... Biotechnology market sectors. This role requires a strong focus on stakeholder management, the ... Oversee and direct construction projects from conception to completion. * Work with customer ...

Senior Project Manager, COA

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

At least five years of relevant experience in clinical localization, clinical operations, clinical technology, or project management within a pharmaceutical, biotechnology, CRO, or related ...

Showing results 41-60

Biotech Project Management information

See Raleigh, NC salary details

$37.4K

$99.8K

$157.5K

How much do biotech project management jobs pay per year?

As of Aug 19, 2026, the average yearly pay for biotech project management in Raleigh, NC is $99,815.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,300.00 and $119,600.00 per year, depending on experience, location, and employer.

What is a biotech project management?

A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.

What are the key skills and qualifications needed to thrive in biotech project management?

To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.

What are the most common challenges faced by professionals in biotech project management?

Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.

What are the most commonly searched types of Biotech Project Management jobs in Raleigh, NC?

The most popular types of Biotech Project Management jobs in Raleigh, NC are:

What are popular job titles related to Biotech Project Management jobs in Raleigh, NC?

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

What job categories do people searching Biotech Project Management jobs in Raleigh, NC look for?

The top searched job categories for Biotech Project Management jobs in Raleigh, NC are:

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

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

Infographic showing various Biotech Project Management job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $99,815 per year, or $48 per hour.

Senior Project Manager - Operational Readiness

PSC Biotech

Raleigh, NC • On-site

$120 - $160/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Job description

Senior Project Manager - Operational Readiness

Raleigh/Durham, United States | Posted on 07/15/2026

PSC Biotech provides essential services to the life sciences, ensuring that health care products are developed, manufactured, and distributed to the highest standards and in compliance with all applicable regulatory requirements.

Our Senior Project Managers lead biopharma projects, providing strategic delivery guidance, reducing execution risk, ensuring regulatory compliance, and optimizing overall project performance.

  • Develop project plans and execution strategies, defining and integrating cross‑functional operational readiness workstreams, proactively driving communication, issue resolution, and execution activities.
  • Develop, manage, and maintain integrated schedules and risk registers.
  • Proactively identify and resolve potential risks, ensuring adherence to quality standards and regulatory requirements.
  • Lead recurring meetings, working sessions, workshops, and execution forums to support progress, issue resolution, and accountability.
  • Partner with other project managers to maintain coordinated execution across interdependent project activities.
  • Effectively communicate project status updates and plans to management.
  • Ensure Operational Readiness plans remain aligned with construction, commissioning, qualification, and overall site readiness activities.
  • Support issue management, gap identification, risk mitigation planning, and cross‑functional decision‑making throughout the project lifecycle.
  • Facilitate workshops to improve team alignment, resolve project challenges, and support broader site strategy and readiness planning.
Requirements
  • Bachelor's or advanced degree in engineering or related life sciences discipline. PMP certification is a plus.
  • Minimum of 10 years leading and managing projects within the life sciences and regulated manufacturing operations.
  • Experience in and strong working knowledge of biologics drug substance manufacturing operations is required.
  • Advanced knowledge of regulatory requirements and guidelines.
  • Proven experience supporting operational readiness and related project execution activities.
  • Strong background supporting biopharma new product introduction, technology transfer, or manufacturing launch/readiness activities.
  • Proven background in and knowledge of validation lifecycle and CQV activities.
  • Experience in manufacturing and operations systems such as Trackwise, LIMS, Maximo, MES, and related.
  • Strong analytical skills to establish strategic plans, identify issues, evaluate progress, and make informed decisions that align with project goals.
  • Strong stakeholder management, communication, and meeting facilitation skills.
  • Ability to work effectively in a matrixed, cross‑functional environment and drive alignment across multiple workstreams and stakeholders.
  • Adaptable and flexible, capable of adjusting plans and strategies in response to evolving requirements, priorities, or constraints.
  • Must be authorized to work in the US.
  • No C2C at this time.
Benefits
  • Medical, Dental, and Vision – PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents.
  • Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability, and related insurance options.
  • 401(k) and 401(k) matching.
  • PTO, sick time, and paid holidays.
  • Education assistance.
  • Pet insurance.
  • Fitness perks and discounted rates.
  • Financial perks and discounts.
Equal Opportunity Employment Statement

PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, the company complies with all applicable federal, state and local laws concerning employment discrimination. Accordingly, discrimination is prohibited in all aspects of employment, including recruitment, interviewing, hiring, evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination, and employer‑sponsored activities. Employment decisions are made without regard to an applicant’s, employee’s, or intern’s actual or perceived race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.

#J-18808-Ljbffr