Project / Validation Engineer at Project Farma

Chicago, Illinois, United States

Project Farma Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
NoVisa
Life Sciences, PharmaceuticalsIndustries

Requirements

  • Bachelor’s Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in CQV engineering, cGMP facility start-up, project management and/or comparable military experience)
  • Authorized to work in the United States on a full-time basis (no sponsorship for work visas)
  • Full-time on-site client presence
  • Willingness to travel as required to support project and business needs
  • Valid driver's license
  • Covid Vaccine required prior to start date (with exceptions for medical and religious accommodations when reasonable)
  • Thrive in a fast-paced environment
  • Detail-oriented with natural leadership qualities
  • Currently or will live in the area where the job is posted
  • Philanthropic drive embodying Patient Focused and People First Mission

Responsibilities

  • Provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes
  • Create alignment with cross-functional client departments including Validation, Manufacturing, Quality, Supply Chain, and Engineering
  • Proactively identify and escalate roadblocks
  • Utilize critical thinking and problem-solving skills to identify creative solutions to problems and roadblocks
  • 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

Skills

Key technologies and capabilities for this role

Validation EngineeringProject EngineeringManufacturing ProcessesQuality AssuranceSupply Chain ManagementTroubleshootingProblem SolvingCritical Thinking

Questions & Answers

Common questions about this position

What are the salary details for this Project Engineer position?

This information is not specified in the job description.

Is this Project Engineer role remote or on-site?

The position requires full-time on-site client presence.

What qualifications are required for the Project Engineer role?

A Bachelor’s Degree in Life Science, Engineering, or related discipline is required, or equivalent work experience in CQV engineering, cGMP facility start-up, project management, or comparable military experience. Candidates must also be authorized to work full-time in the US without sponsorship.

What is the company culture like at Project Farma?

The company features a dynamic, high-performing team of vibrant professionals passionate about innovation, high-quality work, and patient impact in a fast-paced environment. They emphasize a Patient Focused and People First Mission with opportunities for professional development and philanthropy.

What makes a strong candidate for this Project Engineer position?

Strong candidates thrive in fast-paced environments, are detail-oriented with natural leadership qualities, live in the job posting area, are willing to travel significantly, and have hands-on experience in engineering life cycles, validation, and GxP practices.

Project Farma

Biomanufacturing services for cell and gene therapy

About Project Farma

Project Farma specializes in biomanufacturing, focusing on cell and gene therapy. The company develops and implements 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.

Chicago, IllinoisHeadquarters
2016Year Founded
ACQUISITIONCompany Stage
Consulting, Biotechnology, HealthcareIndustries
51-200Employees

Benefits

Health Insurance
Dental Insurance
Vision Insurance
401(k) Company Match
Paid Vacation
Company Paid Maternity and Parental Leave
Continuing Education Assistance

Risks

Emerging biomanufacturing consulting firms increase market competition.
Rapid technological advancements may require significant investment to stay competitive.
Economic downturns could reduce demand from biotech startups.

Differentiation

Project Farma specializes in cell and gene therapy facility builds and compliance.
They offer turnkey solutions, managing projects from planning to execution.
Their focus on philanthropy and professional development sets them apart.

Upsides

Rising demand for cell and gene therapies boosts need for specialized facilities.
Advancements in automation enhance efficiency and cost-effectiveness of services.
Complex regulatory requirements increase demand for Project Farma's consulting expertise.

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