Project Engineer / Senior Project Engineer at Project Farma

Los Angeles, California, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

NoVisa

Pharmaceutical, Life SciencesIndustries

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)
Must live in the area where the job is posted
Willingness to travel as required to support project and business needs
Covid Vaccine required prior to the Team Member’s start date with exceptions for medical and religious accommodations when reasonable
Authorized to work in the United States on a full-time basis (no sponsorship for current or future work visas)
Valid driver's license (cannot employ anyone with an invalid driver's license)

Responsibilities

Provide support and troubleshooting to clients regarding 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
Create alignment with cross-functional client departments including Validation, Manufacturing, Quality, Supply Chain, and Engineering
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

Skills

CQV

cGMP

GxP

SOP

Validation Protocols

Project Management

Troubleshooting

Technical Writing

System Validation

Process Validation

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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