Full-Time

Validation Engineer

Confirmed live in the last 24 hours

Project Farma

Project Farma

51-200 employees

Biomanufacturing services for cell and gene therapy

Consulting
Biotechnology
Healthcare

Compensation Overview

$63.8k - $69.3kAnnually

+ Bonus

Junior, Mid

San Diego, CA, USA

Full time on-site client presence required.

Category
QA & Testing
Quality Assurance
Requirements
  • Bachelor’s degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • Covid Vaccine is required prior to the Team Member’s start date with exceptions for medical and religious accommodations when reasonable.
  • Full time on-site client presence
  • Willingness to travel up to 100% or as required to support project and business needs.
Responsibilities
  • Create alignment with cross-functional client departments including but not limited to Validation, Manufacturing, Quality, Supply Chain, and Engineering.
  • Provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes.
  • Perform due diligence on system and subject domains to generate high-quality project deliverables.
  • Author technical documents such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Execute system and process validation protocols using GxP best practices.
  • Proactively identify and escalate roadblocks and utilize critical thinking skills and knowledge of problem-solving skills to identify creative solutions to those problems and roadblocks.
  • Contribute to and embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.
  • Build meaningful internal and external relationships presenting Project Farma as a service to clients as needed.

Project Farma specializes in biomanufacturing, particularly in the cell and gene therapy market, where they develop strategies for advanced therapy facilities. They provide comprehensive services that include facility construction, regulatory compliance, and project management, ensuring adherence to Good Manufacturing Practices (GMP). Their clients range from biotech startups to pharmaceutical companies, and they charge fees for their consulting services. The company's goal is to enhance patient outcomes by delivering safe and effective therapies through meticulous project execution.

Company Stage

Acquired

Total Funding

N/A

Headquarters

Chicago, Illinois

Founded

2016

Simplify Jobs

Simplify's Take

What believers are saying

  • Rising demand for cell and gene therapies boosts need for Project Farma's expertise.
  • Advancements in automation enhance efficiency, benefiting Project Farma's service offerings.
  • Complex regulatory requirements increase demand for Project Farma's specialized consulting services.

What critics are saying

  • Emerging biomanufacturing consulting firms increase competition for Project Farma.
  • Rapid technological advancements may require significant investment to maintain competitiveness.
  • Economic downturns could reduce demand for Project Farma's consulting services.

What makes Project Farma unique

  • Project Farma specializes in cell and gene therapy facility builds and compliance.
  • They offer end-to-end solutions, from planning to execution, ensuring GMP compliance.
  • Their focus on philanthropy and professional development sets them apart in the industry.

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