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Biotechnology Project Manager Jobs in Delaware (NOW HIRING)

Bloom Energy

Welding Team Lead-Day Shift

Newark, DE

Provide hands on welding support to manufacturing areas and engineering projects * Answer technical ... Cycle counts and inventory management * Create, document, and sustain standardized work practices

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Biotechnology Project Manager information

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$46

$76

How much do biotechnology project manager jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for biotechnology project manager 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 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 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 are popular job titles related to Biotechnology Project Manager jobs in Delaware? For Biotechnology Project Manager jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Delaware look for? The top searched job categories for Biotechnology Project Manager jobs in Delaware are:
What cities in Delaware are hiring for Biotechnology Project Manager jobs? Cities in Delaware with the most Biotechnology Project Manager job openings:
Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Delaware as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $96,267 per year, or $46.3 per hour.

Research Scientist - In vitro DMPK

QPS, LLC

Newark, DE • On-site

$80K - $92K/yr

Full-time

Life, Retirement

Posted 16 days ago

Job description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As a Research Scientist, you will be a key contributor in QPS’ Drug Metabolism and Pharmacokinetics (DMPK) department in the In Vitro group. As the Principal Investigator, incumbent will fill the role of Technical Leader, and be responsible for completing portions of/entire, projects, and providing quality and timely results, as well as collaborating and communicating with Clients, QPS management, and external resources.


QPS’ Story:

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.


Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.


If this sounds like your ideal work environment, then we would love to speak with you, so apply today!


Please visit our website (www.qps.com) for more information and to see all current openings.


The Job

  • Independently understand, recognize and initiate/prepare study protocols and reports.
  • Independently perform in vitro metabolism studies using S9, microsomes, cytosol and cDNA expressed enzymes.
  • Perform cell culture and maintain cell lines, prepare cells and conduct the metabolic as well as drug transport studies.
  • Conduct enzyme induction studies using fresh/cryopreserved human hepatocytes.
  • Isolate and purify mRNA, quantify mRNA by qRT-PCR and determine the enzyme induction status.
  • Simultaneously handle lab work as well as routine projects.
  • Prepare data summaries and data interpretation.
  • Evaluate significance of data and report findings.
  • Supervise, train and/or mentor junior scientists.
  • Prepare materials for presentations and publications.


Work Location

  • This job will be 100% QPS-office/facility based


Requirements

  • The successful candidate will hold an advanced degree in Pharmaceutical Sciences, Biochemistry, Pharmacology, or related scientific discipline as follows:
    • Ph.D. degree
    • Master’s degree with ≥ 6 years’ of relevant experience
  • Understanding of experimental design and planning associated with assigned area, as well as data collection and analysis software.
  • Proven ability to successfully work in a team environment.
  • Excellent oral and written communication skills.
  • Ability to make independent decisions.


Why You Should Apply

  • Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
  • Structured Career Ladders that provide excellent growth based on your personal aspirations.
  • Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
  • Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance
  • Park-like setting in Newark, Delaware
  • Internal committees designed with the needs and enjoyment of QPS employees in mind.


QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.