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Project Manager Biotech Jobs in Delaware (NOW HIRING)

Amazon

Operations Manager

Middletown, DE · On-site

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

QPS, LLC

Safety Officer II - Pharmacovigilance

Newark, DE · On-site

$90K - $100K/yr

QPS is a global, full-service CRO supporting pharmaceutical, biotechnology, and medical device ... Participate in client meetings and project discussions, providing project updates, responding to ...

ChristianaCare

Research Scientist - Gene Editing

Newark, DE · On-site

$73K - $117K/yr

Strong project management skills will be essential for role. At the ChristianaCare Gene Editing ... Master's degree with 4-5 years' experience in molecular biology, biotechnology, cell biology, or a ...

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All JobsProject Manager Biotech JobsProject Manager Biotech Jobs in Delaware

Project Manager Biotech information

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$21

$46

$76

How much do project manager biotech jobs pay per hour?

As of Jun 21, 2026, the average hourly pay for project manager biotech in Delaware is $46.28, according to ZipRecruiter salary data. Most workers in this role earn between $40.19 and $50.77 per hour, depending on experience, location, and employer.

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.

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 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, and why are they important?

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.
What are popular job titles related to Project Manager Biotech jobs in Delaware? For Project Manager Biotech jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Delaware look for? The top searched job categories for Project Manager Biotech jobs in Delaware are:
What cities in Delaware are hiring for Project Manager Biotech jobs? Cities in Delaware with the most Project Manager Biotech job openings:
Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Delaware as of June 2026, with employment types broken down into 100% Full Time. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $96,267 per year, or $46.3 per hour.
6269 - Facilities Project Manager / Project Manager

6269 - Facilities Project Manager / Project Manager

Verista, Inc.

Newark, DE • On-site

Other

Posted 14 days ago

Job description

Facilities Project Manager Job Responsibilities:

  • Lead full lifecycle capital projects with a focus on pharmaceutical utilities and facilities systems (HVAC, clean utilities, WFI, clean steam), ensuring delivery on scope, schedule, and budget
  • Manage concurrent engineering projects including facility upgrades, infrastructure improvements, packaging, and inspection systems
  • Provide technical leadership for GMP-regulated facility and utility projects, ensuring compliance with CQV and validation requirements
  • Develop and control capital budgets and forecasts, track spend, and manage financial performance across projects
  • Oversee construction activities and contractor execution (preferred), including bid evaluation, field coordination, and safety compliance
  • Ensure adherence to project governance, design reviews, change control, and validation documentation (IQ/OQ/PQ)
  • Collaborate cross-functionally with Facilities, Manufacturing, Quality, Validation, and EHS to support site readiness and operational reliability
  • Manage external vendors, contractors, and engineering firms to ensure quality, safety, and timely project delivery

Job Requirements:

  • Bachelor's degree in Engineering required; strong project scheduling, budgeting, and leadership skills expected
  • 7-10+ years of experience in pharmaceutical/biotech environments with a focus on utilities, facilities, and capital projects
  • Advanced proficiency with Microsoft Project or similar tools for complex project scheduling
  • Strong experience in capital budgeting, forecasting, and cost control, particularly for facility and construction projects
  • Strong knowledge of GMP requirements and equipment qualification
  • Deep understanding of pharmaceutical utility systems (HVAC, clean rooms, WFI, clean steam, process gases, building management systems)
  • Experience with facility design, equipment layout, and infrastructure integration
  • Knowledge of GMP requirements, equipment qualification (IQ/OQ/PQ), and validation lifecycle
  • 100% on-site presence required (Newark, DE)

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