Manager, Technical Manufacturing at Project Farma

Houston, Texas, United States

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, PharmaceuticalsIndustries

Requirements

Bachelor’s Degree or Master’s Degree in Life Science, Engineering, or related discipline and/or comparable military experience
Typically, a minimum of 4-6 years of advanced therapy, life science, pharmaceutical, or biotech experience
Typically, 4-6+ years of managing high-performing teams
Typically, 4+ years business development, lead generation, or sales experience
Willingness to travel as required to support project and business needs
Currently or will live in the area where this job is posted
Thrive in a fast-paced environment
Detail-oriented and exhibit natural leadership qualities
Excel as a leader and enjoy increasing your own knowledge base while lifting others up alongside you
Philanthropic drive and embody Patient Focused and People First Mission through professional development and philanthropic opportunities

Responsibilities

Direct, manage, and build high performing teams executing projects within Project Farma's practice areas across various client sites/locations with overall responsibility for technical solutions, cost, quality, and client satisfaction
Represent Project Farma by collaborating with clients as a trusted Partner, Account, Site and/or Project Owner
Set and lead project direction and strategy based on client vision and expected outcomes throughout the entire project delivery life cycle
Lead initiatives and projects by ensuring Team Members understand team and individual goals and responsibilities, managing priorities, and ensuring timely and high-quality completion of work
Act as a Subject Matter Expert providing technical direction, training, career development, and performance assessments for project Team Members
Develop strategies for the success of the service line or market target such as planning, scheduling, estimating, monitoring, progress measurement, risk management, training, and reporting procedures
Manage new and existing client accounts, focusing on project delivery, actively seeking to maintain and grow accounts in line with organizational growth targets
Apply understanding of Project Farma's target industries including how each sector works together, interdependencies, emerging trends, and key challenges to strategic initiatives

Skills

Key technologies and capabilities for this role

CQVCommissioningQualificationValidationProject ManagementTeam LeadershipEngineering ManagementClient CollaborationTechnical SolutionsLife Sciences

Questions & Answers

Common questions about this position

Is this position remote or does it require being in a specific location?

The role requires you to currently live or be willing to live in the area where the job is posted, and involves working across various client sites/locations.

What salary or compensation does this role offer?

This information is not specified in the job description.

What key skills and qualities are needed for the CQV Engineering Manager role?

Candidates need to thrive in a fast-paced environment, be detail-oriented with natural leadership qualities, and excel at leading teams while developing technical expertise in CQV engineering.

What is the company culture like at Project Farma?

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

What makes a strong candidate for this Manager, CQV Engineering position?

Strong candidates thrive in fast-paced environments, demonstrate natural leadership and detail-orientation, love to travel, and align with the company's patient-focused mission while having CQV expertise.

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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