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Pharmaceutical Developer Jobs in Delaware (NOW HIRING)

Prophecy Technologies

R&D CSV Engineer

Wilmington, DE · On-site

The engineer will be responsible for applying core CSV principles and regulatory expertise within a pharmaceutical or life sciences R&D environment. Key Responsibilities: * Ensure strict adherence to ...

Ingersoll-Rand plc

Project Engineer

Frederica, DE · On-site

From space exploration and defense systems to pharmaceutical and industrial applications, ILC Dover ... The Project Engineer supports the successful execution of engineering and production programs ...

New

WuXi AppTec

Engineer - Aseptic Filling

Middletown, DE · On-site

$68K - $88K/yr

The Aseptic Filling Engineer will be a key member of the Engineering Department and serve as the ... Minimum of 5 years of experience in the pharmaceutical or biotechnology industry. * Hands-on ...

New

WuXi AppTec

Engineer - Aseptic Filling

Middletown, DE · On-site

$68K - $88K/yr

The Aseptic Filling Engineer will be a key member of the Engineering Department and serve as the ... Minimum of 5 years of experience in the pharmaceutical or biotechnology industry. * Hands-on ...

New

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All JobsPharmaceutical Developer JobsPharmaceutical Developer Jobs in Delaware

Pharmaceutical Developer information

See Delaware salary details

$17

$52

$81

How much do pharmaceutical developer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for pharmaceutical developer in Delaware is $52.88, according to ZipRecruiter salary data. Most workers in this role earn between $40.43 and $64.71 per hour, depending on experience, location, and employer.

What is a pharmaceutical developer?

Pharmaceutical developers are professionals who design, create, and test new medications and drug therapies. They work on the research and development of pharmaceuticals, ensuring that new drugs are safe, effective, and meet regulatory standards. Their work involves a combination of biology, chemistry, and clinical trials to bring new treatments from the laboratory to the market. Pharmaceutical developers often collaborate with scientists, regulatory agencies, and manufacturers throughout the drug development process.

What are the main challenges a pharmaceutical developer faces during the drug development process?

Pharmaceutical Developers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing lengthy development timelines. Balancing innovation with compliance is crucial, as each stage— from research and formulation to clinical trials— involves rigorous testing and documentation. Collaboration with cross-functional teams like regulatory affairs, quality assurance, and clinical researchers is essential to successfully advance a drug candidate through each development phase.

What are the key skills and qualifications needed to thrive as a pharmaceutical developer, and why are they important?

To thrive as a Pharmaceutical Developer, you need a solid background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree. Familiarity with analytical instruments, Good Laboratory Practice (GLP), regulatory compliance systems, and data analysis software is crucial. Strong problem-solving abilities, attention to detail, and effective teamwork and communication skills help set outstanding professionals apart. These competencies ensure the safe, efficient, and compliant development of new medications in a highly regulated industry.

What is the difference between Pharmaceutical Developer vs Pharmaceutical Scientist?

AspectPharmaceutical DeveloperPharmaceutical Scientist
Required CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fieldBachelor's, Master's, or PhD in Pharmaceutical Sciences, Chemistry, or related field
Work EnvironmentLaboratories, R&D departments, manufacturing settingsResearch labs, academic institutions, pharmaceutical companies
Employer & Industry UsagePharmaceutical companies, biotech firms, R&D centersResearch institutions, pharmaceutical companies, academia
Common Search & ComparisonYesYes

Pharmaceutical Developers focus on designing, developing, and optimizing new drug formulations and delivery methods, often working closely with manufacturing. Pharmaceutical Scientists conduct research to understand drug properties, mechanisms, and efficacy, primarily in laboratory or academic settings. While both roles require similar educational backgrounds and work within the pharmaceutical industry, their core responsibilities differ: development versus scientific research.

How do you become a pharmaceutical developer?

To become a pharmaceutical developer, individuals typically need a bachelor's degree in pharmacy, chemistry, biology, or a related field, followed by relevant experience or advanced degrees such as a master's or Ph.D. in pharmaceutical sciences or medicinal chemistry. Skills in laboratory research, knowledge of drug development processes, and familiarity with regulatory requirements are essential for success in this role.

How much do pharmaceutical developers make?

Pharmaceutical developers typically earn a median annual salary of around $80,000 to $120,000, depending on experience, education, and location. Senior roles or those with specialized skills in drug formulation or regulatory affairs can earn higher salaries, often exceeding $150,000 annually.

What cities in Delaware are hiring for Pharmaceutical Developer jobs?

Cities in Delaware with the most Pharmaceutical Developer job openings:

Pharmaceutical Developer jobs near you
Infographic showing various Pharmaceutical Developer job openings in Delaware as of August 2026, with employment types broken down into 82% Full Time, 6% Part Time, and 12% Contract. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $109,999 per year, or $52.9 per hour.

R&D CSV Engineer

Wilmington, DE • On-site

Prophecy Technologies
Professional, Scientific, and Technical Services • 11 - 50 employees
Learn more about Prophecy Technologiesexternal

Full-time

Posted 28 days ago

Job description

Role Overview:
This role is for a Computer System Validation (CSV) Engineer with strong R&D domain knowledge, focusing on ensuring GxP compliance for various systems. The engineer will be responsible for applying core CSV principles and regulatory expertise within a pharmaceutical or life sciences R&D environment.
Key Responsibilities:
  • Ensure strict adherence to regulatory standards including 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, and ITIL.
  • Author critical validation documentation such as User Requirement Specifications (URS), Functional Specifications (FS), protocols, final reports, and comprehensive validation plans/reports.
  • Conduct activities related to audit/inspection readiness, periodic reviews, access roster management, and audit trail reviews.
  • Manage deviations and Corrective and Preventive Actions (CAPA), ensuring full compliance with Standard Operating Procedures (SOPs) and company policies.
  • Implement risk-based testing methodologies in alignment with Computer Software Assurance (CSA) fundamentals.

Required Skills:
  • Core expertise in Computer System Validation (CSV).
  • In-depth knowledge of regulatory frameworks including 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, and ITIL.
  • Experience in authoring URS/FS, protocols, final reports, and validation plans/reports.
  • High-level understanding of Veeva Vault suites.
  • Proficiency in risk-based testing aligned to CSA fundamentals.
  • Experience with audit/inspection readiness, periodic reviews, access roster, and audit trail reviews.
  • Competence in Deviation/CAPA management and SOP/policy compliance processes.
  • High-level understanding of R&D domains such as Biostatistics, Clinical, Discovery, Medical Affairs, Pharmacovigilance, Regulatory Affairs, RPA GxP BOTs, and R&D AI GxP.

Qualifications:
  • Bachelor of Science OR Bachelor of Technology OR Bachelor's in Pharmacy.
  • Over 8+ years of overall experience.
  • At least 5 years of experience specifically in Computer System Validation for GxP systems.

Preferred Skills:

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