Project/Validation Engineer at Project Farma

Washington, District of Columbia, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, Pharmaceuticals, BiotechnologyIndustries

Requirements

Bachelor’s degree in Life Science, Engineering, or a related discipline and/or comparable military experience
Covid Vaccine required prior to the Team Member’s start date with exceptions

Responsibilities

Create alignment with cross-functional client departments including Validation, Manufacturing, Quality, Supply Chain, and Engineering
Provide hands-on support and troubleshooting for clients navigating the engineering lifecycle 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

Skills

Key technologies and capabilities for this role

GxPValidation ProtocolsSOPsTesting ProtocolsRequirements SpecificationsProject ManagementEngineeringTroubleshootingManufacturing ProcessesQuality ComplianceSupply Chain

Questions & Answers

Common questions about this position

Is this position remote?

Yes, this is a remote position.

What is the salary for this role?

This information is not specified in the job description.

What qualifications are required for this position?

A Bachelor’s degree in Life Science, Engineering, or a related discipline and/or comparable military experience is required.

What is the company culture like at Project Farma?

Project Farma offers a collaborative environment with a commitment to a 'Patient Focused & People First' mission, opportunities for professional development, and philanthropic activities.

What skills make a strong candidate for this role?

Strong candidates will have knowledge of life sciences, GxP best practices, experience with validation protocols, technical writing skills for documents like SOPs and protocols, and critical thinking for troubleshooting and problem-solving.

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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