Manager, Project Controls 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

UnknownVisa

Biomanufacturing, Life Sciences, PharmaceuticalsIndustries

Requirements

Bachelor’s Degree in Life Science
Thrive in a fast-paced environment
Detail-oriented
Natural leadership qualities
Enjoy engaging teams and mentoring others
Currently or will live in the area where this job is posted
Philanthropic drive and embodiment of Patient Focused and People First Mission through professional development and philanthropic opportunities

Responsibilities

Create alignment with cross-functional client departments, including Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering
Produce key project controls deliverables, including:
Budget estimates
Detailed project schedules and milestones
Feasibility estimates, risks, forecasts, and scenario analysis
Project cost reports and trend analysis
Comprehensive monthly project summary reports
Analyze complex project data and deliver clear, articulate, and concise messages to support decision-making
Gain a general understanding of Earned Value Analysis and PO management tools
Maintain internal site tools such as site dashboards, deliverable trackers, etc

Skills

Project Scheduling

Budget Estimation

Risk Analysis

Earned Value Analysis

Cost Reporting

Trend Analysis

Scenario Analysis

Data Analysis

Forecasting

PO Management

Dashboard Management

Deliverable Tracking

Stakeholder Alignment

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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