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Pharmaceutical Software Developer Jobs in Virginia

Arclin

Project Engineer/Project Manager

Richmond, VA · On-site

... pharmaceuticals. These vital, everyday products can't fail, and we're here to give the world an ... similar software. * Strong analytical, organizational, and problem-solving skills. * Excellent ...

Arclin

Project Engineer/Project Manager

Richmond, VA · On-site

... pharmaceuticals. These vital, everyday products can't fail, and we're here to give the world an ... similar software. * Strong analytical, organizational, and problem-solving skills. * Excellent ...

CoolSys

Sales Engineer

Reston, VA · On-site

$75K - $90K/yr

... pharmaceuticals. No wonder Newsweek named CoolSys one of America's Greatest Workplaces! We ... Proficiency with HVAC selection/design software (e.g., AutoCAD, Carrier HAP) and Microsoft Office ...

CoolSys

Sales Engineer

Sterling, VA · On-site

$75K - $90K/yr

... pharmaceuticals. No wonder Newsweek named CoolSys one of America's Greatest Workplaces! We ... Proficiency with HVAC selection/design software (e.g., AutoCAD, Carrier HAP) and Microsoft Office ...

CoolSys

Sales Engineer

Sterling, VA · On-site

$75K - $90K/yr

... pharmaceuticals. No wonder Newsweek named CoolSys one of America's Greatest Workplaces! We ... Proficiency with HVAC selection/design software (e.g., AutoCAD, Carrier HAP) and Microsoft Office ...

CoolSys

Sales Engineer

Reston, VA · On-site

$75K - $90K/yr

... pharmaceuticals. No wonder Newsweek named CoolSys one of America's Greatest Workplaces! We ... Proficiency with HVAC selection/design software (e.g., AutoCAD, Carrier HAP) and Microsoft Office ...

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Showing results 41-60

All JobsPharmaceutical Software Developer JobsPharmaceutical Software Developer Jobs in Virginia

Pharmaceutical Software Developer information

See Virginia salary details

$47.6K

$110.9K

$164.6K

How much do pharmaceutical software developer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for pharmaceutical software developer in Virginia is $110,886.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,200.00 and $128,900.00 per year, depending on experience, location, and employer.

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

To thrive as a Pharmaceutical Software Developer, you need strong programming skills, knowledge of pharmaceutical regulations, and a relevant degree in computer science, software engineering, or a related field. Familiarity with industry-specific tools such as LIMS (Laboratory Information Management Systems), GxP compliance software, and experience with scripting languages like Python or Java are typically required. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring software accuracy. These skills and qualities are vital for developing compliant, reliable software that supports critical pharmaceutical processes and meets regulatory standards.

What is the difference between Pharmaceutical Software Developer vs Medical Software Engineer?

AspectPharmaceutical Software DeveloperMedical Software Engineer
Required CredentialsBachelor's in Computer Science, Life Sciences, or related field; knowledge of pharmaceutical regulationsBachelor's in Computer Science, Biomedical Engineering, or related; familiarity with healthcare standards
Work EnvironmentPharmaceutical companies, biotech firms, regulated labsHospitals, healthcare tech companies, medical device firms
Employer & Industry UsagePharmaceutical industry, biotech, drug developmentHealthcare industry, medical device, clinical software
Common Search & ComparisonYesYes

Pharmaceutical Software Developers focus on creating software for drug development, clinical trials, and pharmaceutical processes, often working within regulated environments. Medical Software Engineers develop applications for patient care, medical devices, and healthcare management. While both roles require programming skills and knowledge of healthcare standards, their primary industries and applications differ.

What does a pharmaceutical software developer do?

A Pharmaceutical Software Developer designs, develops, and maintains software applications that support the pharmaceutical industry. This can include systems for drug discovery, clinical trials management, regulatory compliance, and pharmaceutical manufacturing. These professionals work closely with scientists, pharmacists, and regulatory teams to ensure the software meets industry standards and helps streamline workflows. Their work is critical in ensuring the accuracy, security, and compliance of data within pharmaceutical companies.

How does a pharmaceutical software developer typically collaborate with cross-functional teams in the drug development process?

Pharmaceutical Software Developers work closely with scientists, regulatory experts, and quality assurance teams to build and maintain software that supports research, clinical trials, and compliance. Collaboration often involves regular meetings to gather requirements, troubleshoot data integration issues, and ensure that software aligns with strict industry regulations such as FDA guidelines. Developers play a key role in translating scientific needs into robust digital solutions, making strong communication and teamwork skills essential. This collaborative environment also provides opportunities to learn from diverse disciplines and contribute directly to the success of new drug development.
What are popular job titles related to Pharmaceutical Software Developer jobs in Virginia? For Pharmaceutical Software Developer jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Software Developer jobs in Virginia look for? The top searched job categories for Pharmaceutical Software Developer jobs in Virginia are:
What cities in Virginia are hiring for Pharmaceutical Software Developer jobs? Cities in Virginia with the most Pharmaceutical Software Developer job openings:
Pharmaceutical Software Developer jobs near you
Infographic showing various Pharmaceutical Software Developer job openings in Virginia as of August 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $110,886 per year, or $53.3 per hour.

Engineer II, Manufacturing Engineering

Thermo Fisher Scientific

Middletown, VA • On-site

$64K - $82K/yr

Full-time

Re-posted 12 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 422 frontline employees who took The Breakroom Quiz

196th of 536 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Thermo Fisher Scientific's Clinical Diagnostic Reagents (CDR) group is seeking a Manufacturing / Industrial / Process Engineer to support manufacturing and process development activities for clinical diagnostic reagents. This role will contribute to the design, optimization, validation, and lifecycle support of reagent manufacturing processes within a cGMP, FDA, and ISO 13485 regulated environment.
This position will help drive end-to-end performance of multiple high-volume and high-mix manufacturing lines with a variety of equipment with various levels of automation. They will help lead cross-functional execution of engineering projects and deliver measurable gains in OEE, FPY, scrap, cycle time, changeover, and equipment uptime. They will also help drive engineering improvement initiatives, including tooling and equipment design and automation, and must be able to manage multiple projects simultaneously from scope and feasibility assessment through sustainment and end of life obsolescence.
Location: Middletown, VA. Relocation assistance is NOT provided.
KEY RESPONSIBILITIES:
  • Support daily manufacturing operations to ensure consistent product quality, yield, and throughput
  • Assist in developing, validating, and optimizing manufacturing processes for diagnostic reagent production including formulation, filling, labeling and packaging processes
  • Author, review, and revise controlled documents including SOPs, batch records, work instructions, and validation protocols/reports
  • Participate in process validation activities (IQ/OQ/PQ) and equipment CQV activities
  • Investigate deviations, nonconformances, and CAPAs; lead root cause analysis investigations and implementation of corrective actions
  • Monitor process performance using statistical tools and identify opportunities for improvement
  • Collaborate with Quality, R&D, Regulatory, and Operations teams to ensure compliance with cGMP, FDA, and ISO 13485 requirements
  • Assist with change control activities (MOC), risk assessments, and failure mode analyses
  • Maintain accurate documentation in compliance with data integrity standards (ALCOA+)
  • Support internal and external audits and regulatory inspections as needed
  • Develop equipment tooling design improvements and/or advance levels of equipment automation

REQUIREMENTS/QUALIFICATIONS:
  • Bachelor's Degree in Mechanical Engineering, Industrial Engineering, Biomedical/Biochemical Engineering, Chemical Engineering, or related technical discipline
  • 2-3 years of experience with manufacturing, industrial, or process engineering (within a regulated industry such as Medical Device or Pharmaceutical preferred)
  • Strong mechanical design aptitude and familiarity with equipment and process design lifecycle components from conception through end of line obsolescence
  • Relevant technical certifications or apprenticeships are valued
  • Strong knowledge of cGMP, ISO standards, and regulatory standards
  • Experience with lean manufacturing principles and continuous improvement methodologies
  • Proficient in statistical analysis, root cause investigation, and problem-solving techniques
  • Expertise with CAD software, manufacturing systems, and data analysis tools
  • Experience with engineering documentation, specifications, and change control processes
  • Experience with automation, controls, and equipment/tooling design preferred
  • Knowledge of equipment qualification and process validation
  • Lean Six Sigma Green/Black belt certification a plus
  • Knowledge of aseptic processing or reagent formulation a plus
  • Must be legally authorized to work in the United States without sponsorship.
  • Must be able to pass a comprehensive background check, which includes a drug screening.

Core Competencies
  • Excellent written and verbal communication skills
  • Attention to detail and commitment to quality
  • Proactive mindset with continuous improvement focus
  • Strong project management abilities and experience leading cross-functional initiatives
  • Ability to work in cleanroom environments and comply with required PPE/gowning procedures
  • Proficiency with Microsoft Office suite software
  • Strong analytical and troubleshooting capabilities
  • Ability to mentor and train manufacturing personnel
  • Must be able to occasionally lift up to 50 lbs with assistance

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