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Pharma Validation Jobs (NOW HIRING)

PR · On-site

Bachelor's degree in engineering, life science discipline, or equivalent experience in the pharma/biotech industries. * Highly capable of developing, executing, and reviewing validation life cycle ...

Pharma IT Business Analyst * Proven experience working as a Business Analyst (BA) or Senior ... Partner with Validation teams to support system validation activities and ensure compliance with ...

New

Drive system validation activities in conjunction with Business, IT, Equipment, Validation and QA ... Experience working in life sciences, pharma/biotech, or high-tech industries with a preference for ...

Drive system validation activities in conjunction with Business, IT, Equipment, Validation and QA ... Experience working in life sciences, pharma/biotech, or high-tech industries with a preference for ...

Drive system validation activities in conjunction with Business, IT, Equipment, Validation and QA ... Experience working in life sciences, pharma/biotech, or high-tech industries with a preference for ...

CSPO Job requirements Role: - Pharma Product Manager Location: - Remote JD:-Pharma domain Software ... Familiarity with cloud native software development, validation, audit readiness, and change control ...

CSPO Job requirements Role: - Pharma Product Manager Location: - Remote JD:-Pharma domain Software ... Familiarity with cloud native software development, validation, audit readiness, and change control ...

MES Validation Engineer

Hillsboro, OR · On-site +1

$70 - $80/hr

Experience with MES Pharma Suite Writing is preferred. * Professional certifications such as Certified Quality Engineer (CQE) or Certified Software Validation Specialist (CSVS) are preferred. (H)

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Pharma Validation information

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$22

$51

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How much do pharma validation jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for pharma validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is pharma validation?

Pharma validation is the process of ensuring that pharmaceutical manufacturing processes, equipment, and systems consistently produce products meeting predetermined quality standards and regulatory requirements. This process involves documenting and verifying each step in the manufacturing process to ensure safety, efficacy, and compliance. Validation activities include installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). Proper validation helps minimize risks, ensures patient safety, and is a critical requirement for regulatory approval by agencies like the FDA.

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

To thrive in Pharma Validation, you need a strong background in pharmaceutical sciences, regulatory compliance, and validation protocols, often supported by a relevant degree such as pharmacy, chemistry, or engineering. Familiarity with validation tools, Good Manufacturing Practice (GMP) guidelines, and quality management systems is essential, along with certifications like Six Sigma or Lean Manufacturing being advantageous. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring thorough documentation and collaboration with cross-functional teams. These skills ensure all processes and products meet stringent regulatory standards, safeguarding product quality and patient safety.

What is the difference between Pharma Validation vs Quality Assurance Specialist?

AspectPharma ValidationQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality departments, production sites
Industry UsageEnsures equipment, processes meet standardsMaintains quality systems, audits

Pharma Validation focuses on verifying that equipment, processes, and systems meet regulatory standards through validation protocols. Quality Assurance Specialists oversee overall quality systems, conduct audits, and ensure compliance. While both roles aim to ensure product quality, Validation is more technical and process-specific, whereas QA Specialists handle broader quality management and compliance activities.

What are some typical challenges faced by professionals in pharma validation, and how can they be addressed?

Pharma validation professionals often encounter challenges such as keeping up with ever-evolving regulatory requirements, managing tight project timelines, and ensuring thorough documentation throughout the validation process. Addressing these challenges requires ongoing training on current Good Manufacturing Practices (cGMP), effective project management skills, and close collaboration with cross-functional teams such as quality assurance and production. Proactively communicating with stakeholders and staying organized can help mitigate risks and ensure compliance.
More about Pharma Validation jobs
What cities are hiring for Pharma Validation jobs? Cities with the most Pharma Validation job openings:
What states have the most Pharma Validation jobs? States with the most job openings for Pharma Validation jobs include:
Infographic showing various Pharma Validation job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Applications Engineer - Pharma

Varda Space Industries

El Segundo, CA

$120K - $160K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 15 days 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 any other key operational efficiency. Your contributions will immediately impact functional operations and have 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 the pharma business unit, supporting lab systems, spend tracking, and data automation.
  • Administer and optimize the pharma platform stack (ERP, CRM, ELN, LIMS, QMS) to support current R&D and scale with the clinical pipeline.
  • Build internal applications (low-code and custom-built) that automate repetitive data tasks across the pharma org.
  • Design dashboards and solutions in Power BI, SQL, and Python to surface decisions for pharma leadership.
  • Evaluate and support integrations between LIMS, ELN, instrument software, and downstream data processing.
  • Uphold data integrity, audit logs, and user controls aligned with GxP and FDA 21 CFR Part 11.
  • Build, pilot, and deploy AI-powered tools, including LLM-based agents and generative tooling - across pharma workflows.
  • Lead training and enablement that drives adoption and reduces shadow IT across pharma.

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).
  • 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).
  • Comfortable gathering requirements directly from end users and iterating prototypes to production.
  • Strong written and verbal communication skills with the ability to produce system design documentation, SOPs, and training materials for non-technical pharma stakeholders.

Preferred Skills and Qualifications
  • 3+ years of experience in a pharma-regulated or compliance-driven environment.
  • Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
  • Familiarity with pharmaceutical industry operations, including regulatory submissions, drug lifecycle management, or commercial data flows.
  • Hands-on experience with ETL tools (Alteryx, dbt, SSIS, or Informatica) and cloud data platforms (Snowflake, Databricks, AWS Redshift).
  • Salesforce administration or development experience (Flows or Lightning).
  • Track record of building workflow automation or custom tooling with quantifiable outcomes such as hours saved, error reduction, or user adoption metrics in a regulated environment.
  • Information Technology Infrastructure Library (ITIL), Project Management Professional (PMP), or Lean Six Sigma certification.

Compensation
  • Applications Engineer - Pharma: $120,000 - $160,000/per year
  • Leveling and base salary are determined by job-related skills, education level, experience level, and job
  • performance
  • You will be eligible for long-term incentives in the form of stock options and/or long-term cash awards
  • Offer compensation also includes the ability to purchase company stock through the Employee Stock Purchase Plan

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.
Benefits
Varda offers a comprehensive benefits package designed to support health, financial well-being, and a high-quality workplace experience. Below is an overview of what full-time employees receive (at this time, interns receive a subset of benefits):
Health & Wellness
  • Flexible PTO policy + 12 paid holidays
  • 100% company-paid Medical, Dental, and Vision insurance plans for employees and dependents with FSA and employer-matched HSA options
  • Voluntary accident, hospital, critical illness, and pet insurance
  • $120/month wellness reimbursement for gym and fitness expenses
  • 12 weeks of parental leave (with supplemental disability leave for CA mothers)
  • Family building, pregnancy, parenting and menopause benefits via Maven Clinic
  • Sponsored One Medical memberships for employees and their dependents

Financial & Retirement
  • Substantial incentive equity in a fully funded space start-up
  • 401(k) retirement plan with 6% employer match (immediately vested)
  • $20/pay period cell phone reimbursement
  • Relocation support for new hires, if needed

Workplace Experience & Perks
  • Fully stocked kitchen with lunch provided daily and dinner provided twice weekly
  • Company and team-bonding events, happy hours and mission-success celebrations
  • Complimentary EV charging
  • Dog-friendly office space

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.
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.
E-Verify Notice Right To Work Notice
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