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Biotechnology Project Manager Jobs in Silver Spring, MD

CareMetx

Project Manager

Bethesda, MD · On-site

Project Manager POSITION SUMMARY : The Project Manager (PM) role within the Project Management ... Preferred experience in the pharmaceutical, medical device, biotech or healthcare hub services ...

CareMetx

Project Manager

Bethesda, MD · On-site

Project Manager POSITION SUMMARY : The Project Manager (PM) role within the Project Management ... Preferred experience in the pharmaceutical, medical device, biotech or healthcare hub services ...

Black Canyon Consulting

Project Manager

Bethesda, MD · On-site +1

Overview Black Canyon Consulting (BCC) is actively looking for Project Manager for SRA to support our work for the National Center for Biotechnology Information (NCBI) at the National Library of ...

Black Canyon Consulting

Project Manager

Bethesda, MD · On-site

Overview Black Canyon Consulting (BCC) is actively looking for Project Manager to support our work for the National Center for Biotechnology Information (NCBI) at the National Library of Medicine ...

Black Canyon Consulting

Project Manager

Bethesda, MD · On-site

Overview Black Canyon Consulting (BCC) is actively looking for Project Manager to support our work for the National Center for Biotechnology Information (NCBI) at the National Library of Medicine ...

Black Canyon Consulting

Project Manager

Bethesda, MD · On-site

Overview Black Canyon Consulting (BCC) is actively looking for Project Manager for SRA to support our work for the National Center for Biotechnology Information (NCBI) at the National Library of ...

PharmaOut

Clinical Project Manager

Gaithersburg, MD · On-site

Life sciences or medical background is required. 6+ years of industry experience (biotech/pharma) with at least 2-5 (will determine level) years of project management experience Experience in Phase 1 ...

Dynalectric Company

Project Manager

Dulles, VA

$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 ...

Dynalectric Company

Project Manager

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 ...

Dynalectric Company

Assistant Project Manager

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

Mettler Toledo

Software Project Manager

Columbia, MD · On-site

Manage end-to-end software project lifecycle, aligning with hardware milestones. * Develop and ... biotechnology, and chemical industries the information they need to deliver life-changing products.

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How much do biotechnology project manager jobs pay per hour?

As of May 29, 2026, the average hourly pay for biotechnology project manager in Silver Spring, MD is $47.66, according to ZipRecruiter salary data. Most workers in this role earn between $41.39 and $52.26 per hour, depending on experience, location, and employer.

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 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 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 Silver Spring, MD? For Biotechnology Project Manager jobs in Silver Spring, MD, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Silver Spring, MD look for? The top searched job categories for Biotechnology Project Manager jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Biotechnology Project Manager jobs? Cities near Silver Spring, MD with the most Biotechnology Project Manager job openings:
Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Silver Spring, MD as of May 2026, with employment types broken down into 86% Full Time, 9% Part Time, and 5% Contract. Highlights an 98% Physical, and 2% Hybrid job distribution, with an average salary of $99,129 per year, or $47.7 per hour.

CQV Project Manager

IPS-Integrated Project Services

Germantown, MD • On-site

$107.65K - $143.50K/yr

Full-time

Posted 15 days ago

Job description

Job Description
At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry. We are looking for a dedicated Project Manager of CQV to join our team at our office located in Germantown, Maryland.
In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS' clients. You will follow IPS and client standards and requirements, overall good industry practices for C/Q/V services, and regulatory requirements.
You will also interface directly with IPS clients in the delivery of projects, including routine communications, leading project meetings, tracking, and reporting project metrics (financial and deliverables), self-directing and directing the assigned project team, maintaining positive client relationships, etc. You may also manage and perform standalone commissioning services for non-FDA-regulated clients.
Additional Responsibilities
  • Directly responsible for the successful delivery of commissioning and compliance projects to IPS' clients.
  • Leads multiple concurrent small, mid-sized, or large projects on behalf of IPS.
  • IPS point of contact to the client for overall project delivery. Runs meetings, communicates status and project issues, frequently checks in with client representative(s), and facilitates general project coordination activities.
  • Coordinates project activities with the IPS Project Lead.
  • Perform work to meet IPS budget requirements and quality standards. Provide consistent, complete, and timely feedback and reports to IPS clients or management on project status and issues.
  • Develop project schedules, deliverable tracking reports, scope adjustment notices, etc.
  • Support, train, mentor, and guide commissioning and validation specialists/engineers and project leaders in the delivery of C/Q/V services for assigned projects.
  • Assist or take lead in proposal development, including scope definition, attending bid meetings, development of hours and cost budgets, proposal presentations, etc.
  • Write and manage others in the preparation of C/Q/V documents following established standards and templates, including but not limited to the following:
    • C/Q/V Master Plans
    • Commissioning Forms
    • C/Q/V Protocols and Summary Reports
    • Standard Operating Procedures
    • Impact Assessments
    • Specifications (URS/FRS/DDS)
    • FATS/SATs
  • Perform and manage others during field/site activities, including, but not limited to, the following:
    • Attend and witness FATs and SATs as a representative of IPS clients.
    • Execution of commissioning forms and witnessing of vendor start-up and testing.
    • Execution of C/Q/V protocols.
    • Walkdown and verification of system drawings (P&IDs, as-builts, etc.)
  • Perform and manage staff in compiling data packages and preparing reports for completed C/Q/V activities, including ETOPs, protocol data packages, etc.
  • Responsible for deviation investigation and resolution of problems and issues encountered during field execution activities.
  • Audit project deliverables to assure compliance with established standards.
  • Review the work of the assigned project team.
  • Ensure the quality of the IPS project work.
  • Act as an IPS representative for developing new opportunities and continue to support repeat business.
  • Demonstrated/recognized areas of expertise by industry (Sterile, OSD, Biotech, Medical Device), by equipment/systems (lyos, autoclaves, packaging, compression/encapsulation, etc.), or by validation activity (process, cleaning, CSV, methods, etc.).
  • Provide working knowledge in the delivery of technical projects in these areas.
  • Develop client relationships and act as IPS liaison (point of contact) on project/client sites.
  • Assist in recruiting new staff members and promoting IPS to potential hires.
  • Make recommendations to IPS for possible project and procedural improvements.
  • Other duties as assigned.

The salary range for this role is $107,650 to $143,500, depending on experience and skills.
Qualifications & Requirements
  • Bachelor's degree in Engineering, Project Delivery, or a related discipline, or an equivalent technical degree.
  • 7+ years of experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.
  • Experience with Risk-Based Approach to Commissioning and Qualification.

Preferred Qualifications
  • General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.
  • Experience with Cleaning, Process, Computer System, Methods, and other validation activities and processes.
  • Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software.
  • Project Management Professional (PMP) certification or Professional Engineer (PE) license.

Physical Demands
  • Must be able to: stand, sit, and walk for prolonged periods, stoop, kneel, crouch, and crawl as required.
  • Must be able to lift and move objects weighing up to 50 pounds and climb ladders as necessary.

Work Environment
  • Can work in both indoor and outdoor environments, which may include exposure to varying working conditions.
  • Can adhere to strict cleanroom gowning protocols.

Travel
  • This position will have up to 50% travel, or as required by the assigned project.
  • Position may be assigned to the client site for an extended period.
  • Overnight travel or staying in the city of the Client's location is possible, depending on the assignment.
  • Travel will be per the IPS Travel Policy, client-specific travel policy, or project-specific travel plan.
  • Must have access to reliable transportation.

Safety
  • This position is a safety-sensitive position.
  • The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.

All interviews are conducted either in person or virtually, with video required.
About Us
IPS, a Berkshire Hathaway company, is a global leader in technical consulting, architecture, engineering, procurement, construction management, commissioning, qualification, and validation services for technically complex facilities. Integration is how we think and work. It requires the ability to unite existing and emerging technologies into a process that reliably delivers products and accelerates speed to market. That end-to-end mindset allows us to be agile and anticipate challenges as we move projects toward operational readiness. IPS applies design and delivery expertise, client-side experience, and supplier-side insight to every project. We infuse our curiosity, our passion, and our commitment to partnership in delivering solutions at any scale. We meet our clients where they are and get them to where they need to go. That's only possible when we care as much as our clients do.
Specialties
Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV, and Staffing Services.
All qualified applicants will receive consideration for employment at IPS without regard to race, creed, color, religion, national origin, sex, age, disability, sexual orientation, gender identity or expression, genetic predisposition or carrier status, veteran, marital, or citizenship status, or any other status protected by law. IPS is proud to be an affirmative action and equal opportunity employer.
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