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Biotech Director Project Management Jobs in Delaware

Croda

Head of Project Management

New Castle, DE · On-site

Being involved as a project manager and not solely as a discipline lead. • Former direct people management experience. • Prior commissioning experience • Experience on the owners' side within a ...

HK Recruiting

Program Director R&D PMO

Newark, DE · On-site +1

As Program Director, R&D PMO, you will provide strategic program management and operational leadership for the execution of high-impact programs, guiding them from development through ...

Sobieski

Assistant Project Manager

Newark, DE · On-site

$50K - $60K/yr

... management, or architecture OR associate degree with equivalent work-related experience * 0-3 years of direct project experience in the construction industry * Knowledge of mechanical systems ...

Hologic

Program Director, R&D PMO

Newark, DE · On-site

$170K - $303K/yr

As Program Director, R&D PMO , you will provide strategic program management and operational leadership for the execution of high-impact programs, guiding them from development through ...

Hologic Inc.

Program Director, R&D PMO

Newark, DE · On-site +1

$170K - $303K/yr

As Program Director, R&D PMO , you will provide strategic program management and operational leadership for the execution of high-impact programs, guiding them from development through ...

ATI Restoration

Project Director

Wilmington, DE · On-site

Project Director FLSA Status: Salaried, Exempt Status: Full-Time Position Summary The Project ... Support Project Manager to resolve scope discrepancies and customer concerns; ensure project ...

ATI Restoration

Project Director

Wilmington, DE · On-site

Position Summary The Project Director (PD) is a client-facing, revenue-generating, role responsible ... Support Project Manager to resolve scope discrepancies and customer concerns; ensure project ...

ABB

Data Center COE Project Management Leader

DE · Remote

$119K - $190K/yr

Director, Data Center Services Center of Excellence __ This role leads the performance, quality ... Manage a team and oversee portfoliolevel project management through reviews, proper project closure ...

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Biotech Director Project Management information

What does a Biotech Director of Project Management do?

A Biotech Director of Project Management oversees the planning, execution, and successful completion of projects within a biotechnology organization. They coordinate cross-functional teams, manage timelines, budgets, and resources, and ensure that projects align with the company's strategic goals. This role also involves risk management, stakeholder communication, and compliance with industry regulations. Ultimately, they are responsible for delivering projects on time and within scope, contributing to the company's innovation and growth.

What is the difference between Biotech Director Project Management vs Biotech Project Manager?

AspectBiotech Director Project ManagementBiotech Project Manager
CredentialsAdvanced degrees (MBA, PhD), PMP certification often preferredBachelor's or Master's degree, PMP or similar certification beneficial
Work EnvironmentStrategic leadership, overseeing multiple projects and teamsDay-to-day project execution, managing specific projects
ResponsibilitiesSetting project goals, resource allocation, stakeholder communicationPlanning, executing, and monitoring individual projects

The Biotech Director Project Management typically holds a higher strategic role, overseeing multiple projects and teams, while the Biotech Project Manager focuses on managing specific projects' execution. Both roles require strong project management skills, but the director's position involves broader leadership and strategic planning.

What are the key skills and qualifications needed to thrive as a Biotech Director of Project Management, and why are they important?

A Biotech Director of Project Management requires expertise in project management methodologies, a strong background in life sciences, and advanced degrees such as a PhD or MBA. Familiarity with project management tools like MS Project, regulatory systems (FDA/EMA), and certifications such as PMP are commonly expected. Exceptional leadership, strategic planning, and communication skills help drive cross-functional teams and stakeholder engagement. These competencies ensure successful project delivery, regulatory compliance, and alignment with organizational objectives in the complex biotech environment.

How does a Biotech Director of Project Management typically collaborate with cross-functional teams to ensure project success?

A Biotech Director of Project Management often acts as a central liaison between research scientists, regulatory affairs, clinical operations, and commercial teams. They coordinate project timelines, facilitate regular progress meetings, and ensure that all stakeholders are aligned on goals and deliverables. Effective communication and conflict resolution skills are essential, as the director must navigate differing priorities and integrate feedback from various departments. This collaborative approach helps to mitigate risks, address challenges early, and keep projects on track for timely completion.
What are popular job titles related to Biotech Director Project Management jobs in Delaware? For Biotech Director Project Management jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Biotech Director Project Management jobs in Delaware look for? The top searched job categories for Biotech Director Project Management jobs in Delaware are:
What cities in Delaware are hiring for Biotech Director Project Management jobs? Cities in Delaware with the most Biotech Director Project Management job openings:
Biotech Director Project Management jobs near you
Infographic showing various Biotech Director Project Management job openings in Delaware as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 88% Full Time, 4% Part Time, 4% Contract, and 2% Summer. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution.
Senior Manager, Biologics CMC Project Management

Senior Manager, Biologics CMC Project Management

Incyte Corporation

Wilmington, DE • On-site

Full-time

Posted 9 days ago

Job description

Overview
Job Summary (Primary function)
As a member of the Incyte Technical Operations (Tech Ops) Global Biologics Development (GBD) group, the Senior Manager, Biologics CMC Project Management provides project management leadership and operational coordination for assigned biologics CMC programs, workstreams, or cross-functional initiatives across development stages. The role partners with the GBD technical lead and cross-functional stakeholders to support translation of program strategy into integrated development plans, track priorities, identify risks and dependencies, and help drive timely, aligned execution across Tech Ops, Discovery, Regulatory Affairs, Quality, Supply Chain, and external partners, including CMOs, CROs, and collaborators. The Senior Manager coordinates cross-functional project team activities, supports scenario planning, governance preparation, and decision-ready project communications, and contributes to consistency, visibility, and execution discipline across assigned programs and project management practices.
Essential Functions of the Job (Key Responsibilities)
  • Coordinate and help drive cross-functional project team activities for assigned biologics CMC programs, workstreams, or initiatives, supporting alignment on priorities, deliverables, critical path activities, and execution across functions.
  • Develop and maintain integrated, phase-appropriate project plans that connect CMC, regulatory, technical, and operational activities, and identify dependencies, constraints, and key decision points for review with program/project leadership.
  • Identify, track, and help escalate risks and issues that could affect scope, timelines, cost, quality, or supply, and support mitigation planning and follow-up actions.
  • Support resource and budget tracking for assigned programs by maintaining key assumptions, inputs, trade-offs, and program impacts for review with functional and GBD leadership.
  • Support governance preparation by compiling program status, scenarios, risks, options, and proposed next steps to enable timely and informed decision-making.
  • Coordinate project management activities with external partners, including CMOs, CROs, and collaborators, to support alignment on plans, deliverables, risks, and execution milestones.
  • Maintain dashboards, integrated project timelines, and team SharePoint sites, ensuring project information is current, accurate, and decision ready.
  • Support execution of mid- to late-stage CMC deliverables, including submission-related timelines, readiness activities, and life cycle management tracking for commercial products as needed.
  • Support onboarding, knowledge sharing, and best practices with peers and junior colleagues as appropriate and contribute to continuous improvement of biologics CMC project management tools and ways of working.

Qualifications/Professional Experience Requirements
  • Relevant experience supporting or managing cross-functional biologics product development projects, workstreams, or program deliverables is required.
  • Experience coordinating CMC project activities within the pharmaceutical/biotech industry is required.
  • Understanding of phase-appropriate CMC development and regulatory submission requirements is preferred.
  • Strong project management, communication, and facilitation skills with the ability to influence without authority are required.
  • Experience supporting resource tracking, budget inputs, and program reporting is preferred.
  • Experience with monoclonal antibody drug development is advantageous.
  • Minimum of 4-6 years of project management and/or product development experience within the pharmaceutical/biotech industry, or equivalent skills and knowledge, is required.
  • Degree, such as BS/MS/PhD, in Biological Sciences or related discipline, or equivalent experience.
  • PMP certification and strong technical background are preferred but not required.
  • Willingness to travel as needed - occasional international travel to partner(s) and CMO facilities, with accommodations available for individuals with disabilities.
  • Excellent interpersonal skills with the ability to adapt effectively to changes in organization, structures, and dynamics.
  • Collaborative, self-motivated, organized, and capable of problem-solving, sound judgment, and managing multiple priorities.
  • Excellent written, verbal, and presentation skills.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
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