Consultant / Sr Consultant, CQV Engineering at Project Farma

Raleigh, North Carolina, 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

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
Authorized to work in the United States on a full-time basis (no sponsorship for work visas)
Valid driver's license
Full-time on-site client presence
Willingness to travel as required to support project and business needs (significant travel may be required)
Covid Vaccine required prior to start date (with exceptions for medical and religious accommodations when reasonable)
Currently or will live in the area where the job is posted
Thrive in a fast-paced environment
Detail-oriented and exhibit natural leadership qualities
Enjoy engaging teams and mentoring others
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, 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

Key technologies and capabilities for this role

CQVCommissioningQualificationValidationGMPProject ManagementManufacturing ProcessesTechnical DocumentationCross-Functional CoordinationLeadership

Questions & Answers

Common questions about this position

Is travel required for this CQV Engineering Consultant role?

Yes, this position may require significant travel to support project and business needs.

What is the salary for the Consultant / Sr Consultant, CQV Engineering position?

This information is not specified in the job description.

What skills and qualities are required for this CQV Engineering Consultant role?

Candidates must thrive in a fast-paced environment, be detail-oriented with natural leadership qualities, enjoy engaging and mentoring teams, and have strong collaboration and presentation skills.

What is the company culture like at Project Farma?

Project Farma has a dynamic, high-performing team of vibrant professionals passionate about innovation, delivering high-quality work, and a Patient Focused and People First Mission with professional development and philanthropic opportunities.

What makes a strong candidate for this CQV Engineering Consultant position?

Strong candidates are driven by innovation, thrive in fast-paced environments, love to travel, exhibit leadership and mentoring skills, and align with the Patient Focused and People First Mission.

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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