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Pharma Software Jobs (NOW HIRING)

Rhodes Wolfe

$200K/yr

Director, Consultative Sales - Pharma & Life Sciences Location: United States (Must reside in ... To be successful in this role, you must bring experience selling end-to-end custom software and ...

US Tech Solutions

Software Engineer

Indianola, PA

Title: Software Engineer Duration: 12Months Location: Indianola,PA,15051 Candidate must have a ... Thanks & Regards, Pramod Sharma Clinical/Pharma Recruiter 10 Exchange Place, Suite # 1820 Jersey ...

ARL

Software Developer

Oklahoma City, OK · On-site

$65K - $80K/yr

ARL Bio Pharma is the leading Pharmeceutical testing Company in the nation with a stellar reputation for quality science and reliability. We are seeking a skilled Software Developer with experience ...

Collins Consulting

Customer Service - Pharma

Lake Forest, IL · Hybrid

$15.75 - $21.50/hr

Pharma Customer Service - Demonstrates the ability to work collaboratively, gives customer service ... Must have proven skills in the following PC software products MS Outlook, MS Excel, MS Word. The ...

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How much do pharma software jobs pay per year?

As of Jun 9, 2026, the average yearly pay for pharma software in the United States is $174,017.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,500.00 and $205,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Pharma Software position, and why are they important?

To succeed in Pharma Software roles, you need strong skills in software development or engineering, a solid understanding of pharmaceutical industry regulations (such as FDA or GxP), and often a degree in computer science or a related field. Familiarity with programming languages like Python or Java, experience with validated systems, and knowledge of tools such as LIMS, ERP, or electronic lab notebooks are commonly required. Strong analytical thinking, teamwork, and effective communication set outstanding candidates apart. These abilities ensure the delivery of compliant, secure, and efficient software solutions essential for pharmaceutical operations.

What types of projects or software systems do Pharma Software professionals typically work on?

Pharma Software professionals commonly work on systems that support drug development, clinical trials, laboratory data management, and regulatory compliance, such as LIMS (Laboratory Information Management Systems), electronic data capture tools, and manufacturing execution systems. Daily tasks often include collaborating with scientists, regulatory teams, and other IT specialists to design, validate, and maintain software that must meet stringent industry regulations. This role offers unique opportunities to work at the intersection of technology and life sciences, providing valuable insights into both software engineering and pharmaceutical workflows. As you gain experience, there are career paths toward leading project teams, specializing in systems validation, or advancing into IT management within the pharmaceutical sector.

What is a Pharma Software job?

A Pharma Software job involves developing, implementing, and maintaining software solutions tailored for the pharmaceutical industry. Professionals in this role work on applications that support drug development, regulatory compliance, clinical trials, and supply chain management. They collaborate with healthcare professionals, regulatory bodies, and IT teams to ensure software meets industry standards and enhances efficiency. Skills in programming, data management, and knowledge of pharma regulations like FDA and GxP are often required.

More about Pharma Software jobs
What cities are hiring for Pharma Software jobs? Cities with the most Pharma Software job openings:
What states have the most Pharma Software jobs? States with the most job openings for Pharma Software jobs include:
What job categories do people searching Pharma Software jobs look for? The top searched job categories for Pharma Software jobs are:
Pharma Software jobs near you
Infographic showing various Pharma Software job openings in the United States as of June 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $174,017 per year, or $83.7 per hour.

Pharma Applications Engineer

Varda Space Industries

El Segundo, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 23 hours ago

Job description

About Varda
Low Earth orbit is open for business. Varda is accelerating the development of commercial space infrastructure, from in-orbit pharmaceutical processing to reliable and economical reentry capsules.
From life-saving pharmaceuticals to more powerful fiber optics, there is a world of products used on Earth today that can only be manufactured in space. Varda is accelerating innovation in the orbital economy by creating both the products and infrastructure needed so space can directly benefit life on Earth. Our mission is to expand the economic bounds of humankind.
Our team is uniquely suited to accomplishing this goal, with leadership and staff comprised of veterans from SpaceX, Blue Origin, major pharmaceutical companies and Silicon Valley. Varda was founded in January 2021 by Will Bruey and Delian Asparouhov with significant backing from world class investors including Khosla Ventures, Lux Capital, Founders Fund, Caffeinated Capital, General Catalyst, and Also Capital.
Varda is headquartered in El Segundo, California, where we have offices and a production facility where our vehicles, equipment, and materials are built, integrated, and tested. Varda also has offices in Washington, DC and Huntsville, AL.
Join Varda, and work to create a bustling in-space ecosystem.
About This Role
Varda is seeking a Pharma Applications Engineer to join our team. In this role, you will be responsible for leading efforts to develop, deploy, improve, and manage all Pharma applications. You will manage the implementation of these solutions through the entire product life cycle, from opportunity identification to support and sustainment. You will work cross-functionally with teams across Varda to lead initiatives to enhance company processes, execution insight, and infrastructure robustness. Projects will include a wide range of desired outcomes, including cycle time reduction, cost reduction, improved decision-making, risk reduction, and other key operational efficiencies. Your contributions will immediately impact functional operations and provide an opportunity to contribute to Varda's overall growth and success. This role will report to the Director of Enterprise Applications.
This is a full-time, exempt position located in our El Segundo headquarters.
Responsibilities
  • Serve as the embedded technology partner for a pharmaceutical business unit, supporting data management solutions to facilitate spend tracking and automation for data analysis, while administering core lab systems to ensure data integrity and compliance readiness.
  • Administer and optimize enterprise platforms (ERP, CRM, ELN, LIMS, QMS) to support current R&D needs while preparing to scale with clinical pipeline.
  • Design and build custom analytics dashboards and reports using tools like Power BI, SQL, and Python to help facilitate spend tracking.
  • Enable systems to help automate manual data management tasks to help eliminate manual bottlenecks, ensure compliance with best practices with respect to ELN/LIMS and/or QMS to reduce cycle times, and improve data capture at the source.
  • Develop and maintain internal applications (low-code/no-code and custom-built) that automate repetitive tasks and augment data tasks across the pharma org.
  • Evaluate and support integrations between LIMS, ELN, instrument software, and downstream data processing tools that balance speed-to-value with long-term maintainability.
  • Where needed, support data integrity principles, audit logs, and user controls that are aligned with compliance standards GxP, FDA 21 CFR Part 11)
  • Provide desktop support to resolve application issues, coordinate with vendors on escalations, and manage release cycles for system updates and patches.
  • Create training materials and lead hands-on enablement sessions to drive user adoption and reduce shadow IT across the pharma organization.
  • Support evaluation, pilot, and deployment of AI-powered tools to enterprise standards.
  • Facilitate and enable data governance and quality standards set by the pharma organization
  • Assist IT and Infosec with permissions-based access, tracking, and compliance.
  • Evaluate new tools, platforms, and vendors to support make/buy decisions for data systems to ensure pharma systems integrate cleanly into the broader enterprise architecture.
  • Track and report on system health, adoption KPIs, and project status to pharma leadership and enterprise stakeholders.

Basic Qualifications
  • Bachelor's degree in Computer Science, Information Systems, Data Analytics, Engineering, or a related technical field.
  • 3+ years of experience supporting or managing enterprise applications (ERP, CRM, QMS, or LIMS) in a pharma-regulated or compliance-driven environment.
  • The capability to gather business requirements from stakeholders and take a project from initial concept to finished product.
  • Ability to work with end users to rapidly iterate prototype applications by solving end-user issues.
  • Hands-on experience with business process mapping and re-engineering using structured methodologies.
  • Ability to work independently as the sole technical resource within a business unit, managing competing priorities without day-to-day technical oversight.
  • Ability to translate technical concepts to non-technical audiences for stakeholders, internal and external to the organization.
  • Proficiency in SQL and at least one scripting/programming language (Python, JavaScript, or similar).
  • Demonstrated experience building reports and dashboards in a BI platform (Power BI, Tableau, or equivalent).
  • Familiarity with regulated industry data domains and willingness to develop deep expertise in pharmaceutical data standards and workflows.
  • Familiarity with data integration patterns (ETL/ELT) and tools such as Alteryx, dbt, SSIS, or Informatica.
  • Strong written and verbal communication skills with the ability to produce system design documentation, SOPs, and training materials for non-technical pharma stakeholders.
  • Familiarity with AI/ML concepts and hands-on experience using LLM-based tools in a professional setting.
  • Familiarity with version control systems (Git) and software development lifecycle fundamentals, including code review and CI/CD practices.

Preferred Skills and Qualifications
  • Graduate degree in Computer Science, Information Systems, or related fields.
  • 5+ years of experience supporting or managing enterprise applications (ERP, CRM, QMS, or LIMS) in a pharma-regulated or compliance-driven environment.
  • Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
  • Proficiency with low-code/no-code platforms (Alteryx, Power Apps, or similar) for rapid application development.
  • Experience with cloud data platforms (Snowflake, Databricks, AWS Redshift) and modern ELT architectures.
  • Experience with Microsoft products (Teams, Jira, Confluence, Bitbucket) and their APIs
  • Proven track record of architecting and sustaining AI-powered solutions that drove measurable adoption across large user populations.
  • Salesforce administration or development experience (Flows or Lightning).
  • Experience with aerospace and defense enterprise systems, manufacturing workflows, or supply chain operations, enabling cross-functional impact beyond the pharmaceutical business unit.
  • Information Technology Infrastructure Library (ITIL), Project Management Professional (PMP), or Lean Six Sigma certification.
  • Track record of building workflow automation or custom tooling that eliminated manual processes, with quantifiable outcomes such as hours saved, error reduction, or user adoption metrics in a regulated environment.
  • Familiarity with pharmaceutical industry operations, including regulatory submissions, commercial data flows, or drug lifecycle management.
  • Experience conducting or contributing to platform trade studies or build-vs-buy evaluations for data infrastructure.

Pay Range
  • Salary range: $120,000 - $160,000/per year
  • This role is on-sitein El Segundo, CA
  • Leveling and base salary are determined by job-related skills, education level, experience level, and job performance
  • You will be eligible for incentives in the form of stock options and/or long-term cash awards

ITAR Requirements
  • Varda, like all employers, must ensure that its employees working in the United States are lawfully authorized to work in the U.S. Additionally, our employees are exposed to and have access to certain export-controlled items. At present, some of our technology to which employees have access requires a license to be exported to individuals other than "U.S. Persons" as defined in U.S. export regulations. Because our employees are provided access to export-controlled items, our current policy is to only hire "U.S. persons" who are permitted to have access to our technology without an export license.
    "US person" means: U.S. citizen, U.S. lawful permanent resident, or protected individual as defined by 8 U.S.C. 1324b(a)(3) (i.e., individual admitted to the U.S. as a refugee or granted asylum in the U.S.)
    Learn more about the ITAR here.
Benefits
  • Exciting team of professionals at the top of their field working by your side
  • Equity in a fully funded space startup with potential for significant growth (interns excluded)
  • 401(k) matching (interns excluded)
  • Unlimited PTO (interns excluded)
  • Health insurance, including Vision and Dental
  • Lunch and snacks provided on site every day. Dinners provided twice a week.
  • Maternity / Paternity leave (interns excluded)

Varda Space Industries is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Candidates and employees are always evaluated based on merit, qualifications, and performance. We will never discriminate on the basis of race, color, gender, national origin, ethnicity, veteran status, disability status, age, sexual orientation, gender identity, martial status, mental or physical disability, or any other legally protected status.
E-Verify Statement
Varda Space Industries, Inc. participates in the U.S. Department of Homeland Security E-Verify program. The E-Verify program is an Internet-based employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Learn more about the E-Verify program.
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