Pharma Applications Engineer

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.

• →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.

• 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.

• 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.

• Salary range: $120,000 - $160,000/per year
• This role is on-site in 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

• 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.  

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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