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Full-Time

Utilities Engineering Consultant

Confirmed live in the last 24 hours

Project Farma

Project Farma

51-200 employees

Biomanufacturing services for cell and gene therapy

Consulting
Biotechnology

Compensation Overview

$50k - $240kAnnually

+ Bonus

Mid

Raleigh, NC, USA

Candidate must currently live or will live in the Raleigh area.

Category
Thermal and Fluid Systems Engineering
Mechanical Engineering
Requirements
  • Bachelor’s Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Full-time on-site client presence.
  • Willingness to travel as required to support project and business needs.
  • Covid Vaccine is required prior to the Team Member’s start date with exceptions for medical and religious accommodations when reasonable.
Responsibilities
  • Participate in and lead technical sessions in aspects of cleanrooms, laboratory, and general building HVAC and building mechanical systems engineering & design.
  • Develop creative and innovative solutions to HVAC and Building Mechanical Engineering challenges.
  • Coordinate vendor startup and execution activities for Site Acceptance Testing.
  • Support and lead system startup activities for GMP Clean and Plant Utilities (such as WFI, Clean Steam, Waste, and Air systems).
  • Comply with Current Good Manufacturing Practices to ensure HVAC and Building Mechanical systems are compliant.
  • Writing and documenting technical reports and reviewing field turnover packages.
  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.

Project Farma specializes in biomanufacturing, focusing on cell and gene therapy. They develop and implement strategies for advanced therapy facilities, helping clients create treatments that modify genes to address diseases. Their services encompass the entire lifecycle of biomanufacturing projects, including facility construction, validation, quality assurance, regulatory compliance, and automation. Project Farma distinguishes itself by offering comprehensive, turnkey solutions that ensure facilities meet Good Manufacturing Practices (GMP), which is essential for producing safe therapies. Their goal is to enhance patient outcomes through effective project execution and they also emphasize philanthropy and professional development within their team.

Company Stage

Acquired

Total Funding

N/A

Headquarters

Chicago, Illinois

Founded

2016

Simplify Jobs

Simplify's Take

What believers are saying

  • Acquisition by Precision Medicine Group could provide additional resources and market reach, enhancing Project Farma's service offerings.
  • Their comprehensive service model covering the entire lifecycle of biomanufacturing projects offers employees diverse opportunities for skill development.
  • Strong philanthropic initiatives and a focus on professional development create a fulfilling work environment.

What critics are saying

  • The niche focus on cell and gene therapy could limit market opportunities compared to broader biomanufacturing services.
  • Integration challenges post-acquisition by Precision Medicine Group could lead to operational disruptions.

What makes Project Farma unique

  • Project Farma specializes in the cell and gene therapy market, offering end-to-end biomanufacturing solutions, unlike competitors who may focus on broader pharmaceutical services.
  • Their turnkey solutions ensure GMP compliance from initial planning to final execution, providing a seamless experience for clients.
  • A strong focus on philanthropy and professional development, such as the PF Cares Weekend, sets them apart in terms of corporate culture and employee engagement.

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