CQV Engineering Consultant at Project Farma

Boston, Massachusetts, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, PharmaceuticalsIndustries

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
Thrive in a fast-paced environment
Detail-oriented and exhibit natural leadership qualities
Enjoy engaging teams and mentoring others
Currently or will live in the area where this job is posted
Philanthropic drive and embody Patient Focused and People First Mission

Responsibilities

Coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes
Lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion
Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc
Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentation skills
Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills
Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way
Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan

Skills

CQV

Commissioning

Qualification

Validation

SOP Development

Testing Protocols

Technical Documentation

GMP

Pharmaceutical Engineering

Project Leadership

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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