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Biotechnology Project Manager Jobs in Virginia (NOW HIRING)

PSC Biotech

CQV Project Lead

Richmond, VA · On-site

Bachelor's degree in Engineering, Life Sciences, Biotechnology, or a related technical discipline. * 8+ years of experience in CQV, Validation, Engineering, or Project Management within the ...

EMCOR Group Inc

Dynalectric Company

Dulles, VA · On-site

$70K - $100K/yr

... biotech, healthcare, commercial, transportation, and technology companies, as well as many ... Plan and organize a project under the directions of a Project Manager or Senior Project Manager

ATCC Biotechnology

Partnerships Manager

Manassas, VA · On-site

$125 - $150/hr

... sciences, biotechnology, pharmaceutical, diagnostics, technology, academic, or research ... Experience managing multiple projects, opportunity pipelines, timelines, dashboards, metrics, and ...

KBR

Project Controls Lead

Richmond, VA

Bachelor's degree in Engineering, Project Management, Business, Finance, or a related discipline. * Minimum 15 years of project controls experience, supporting pharmaceutical, biotechnology, life ...

KBR, Inc.

Project Controls Lead

Richmond, VA · On-site

Bachelor's degree in Engineering, Project Management, Business, Finance, or a related discipline. * Minimum 15 years of project controls experience, supporting pharmaceutical, biotechnology, life ...

EMCOR Group Inc

Dynalectric Company

Dulles, VA · On-site

$100K - $125K/yr

... biotech, healthcare, commercial, transportation, and technology companies, as well as many ... Execute and manage all terms of project contracts. * Partner with Foreman, Project Engineers ...

EMCOR Group Inc

Dynalectric Company

Dulles, VA · On-site

$26.40 - $36.06/hr

For both new construction and renovation projects, we offer design-build/design-assist, value ... Enter purchase orders into software systems (Viewpoint & Material Management). * Reconcile all ...

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Biotechnology Project Manager information

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How much do biotechnology project manager jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for biotechnology project manager in Virginia is $45.85, according to ZipRecruiter salary data. Most workers in this role earn between $39.81 and $50.29 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 Virginia?

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

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

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

What cities in Virginia are hiring for Biotechnology Project Manager jobs?

Cities in Virginia with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Virginia as of September 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $95,359 per year, or $45.8 per hour.

CQV Project Lead

Richmond, VA • On-site

PSC Biotech
Biotechnology Research and Development • 51 - 200 employees
Learn more about PSC Biotechexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago

Job description


Our goal is to skyrocket our clients' success, and you can be a part of our team's achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success.
The Experience
With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.
We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.
At PSC Biotech®, it's about more than just a job-it's about your career and your future.
Your Role
We are seeking an experienced CQV Project Lead to lead the planning, coordination, and execution of C&Q activities for advanced biologics manufacturing projects. The CQV Project Lead will be responsible for ensuring the successful mobilization of C&Q teams, managing project schedules and resource forecasts, and overseeing the delivery of C&Q activities throughout the project lifecycle. This position requires strong pharmaceutical industry experience, exceptional project management skills, and the ability to effectively coordinate cross-functional stakeholders to ensure projects are executed safely, compliantly, and on schedule
This is a full role based in Richmond, VA, with an anticipated start of Mid-January 2027.
  • Lead and oversee C&Q activities from project initiation through closeout, ensuring alignment with project objectives, timelines, and regulatory requirements.
  • Ensure successful mobilization, onboarding, and coordination of C&Q teams to support project execution.
  • Develop, maintain, and manage project schedules, resource forecasts, and staffing plans to support successful project delivery.
  • Provide oversight of commissioning, qualification, and validation activities, ensuring deliverables are completed in accordance with approved plans and quality standards.
  • Coordinate C&Q activities across Engineering, Manufacturing, Quality Assurance, Validation, and Operations organizations.
  • Monitor project progress, identify risks and issues, and implement mitigation strategies to maintain schedule and budget commitments.
  • Manage external vendors, contractors, and consulting partners supporting C&Q execution.
  • Ensure documentation, protocols, reports, and turnover packages meet GMP and regulatory requirements.
  • Prepare and communicate project status updates, resource requirements, risks, and milestones to clients and senior stakeholders.
  • Support continuous improvement initiatives and promote best practices in C&Q project execution and project management.

Requirements
  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, or a related technical discipline.
  • 8+ years of experience in CQV, Validation, Engineering, or Project Management within the pharmaceutical or biotechnology industry.
  • Demonstrated experience supporting advanced biologics manufacturing facilities and operations.
  • Proven experience leading CQV projects and managing cross-functional teams in GMP-regulated environments.
  • Strong experience developing and managing project schedules, resource forecasts, and staffing plans.
  • Experience overseeing commissioning, qualification, and validation activities, including IQ/OQ/PQ execution and validation documentation.
  • Working knowledge of cGMP regulations, FDA requirements, and industry best practices related to CQV execution.
  • Excellent organizational, leadership, communication, and stakeholder management skills.
  • Experience managing multiple project priorities, vendors, and contractors in a fast-paced project environment.
  • Proficiency with project scheduling and planning tools such as Microsoft Project, Smartsheet, Primavera P6, or equivalent.

Benefits
Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.
  • Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
  • Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more.
  • 401(k) and 401(k) matching
  • PTO, Sick Time, and Paid Holidays
  • Education Assistance
  • Pet Insurance
  • Discounted rate at Anytime Fitness
  • Financial Perks and Discounts

In accordance with Virginia's laws on pay transparency, the hourly rate for this role is set between $60 - $80. The pay offered may be adjusted based on various factors such as the applicant's qualifications, skills, and professional experience.
Equal Opportunity Employment Statement
PSC Biotech is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs,including wellness, social and recreational programs. Employment decisions will be 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.
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