Project Farma (PF)
Consultant, Project Controls Engineering
Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a Consultant, Project Controls Engineering. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe.
If you are looking for a career accelerator, are driven by innovation, thrive in a fast‑paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.
About the Role As a Project Controls Engineering Consultant, you will work collaboratively with clients, vendors, contractors, and other Project Farma Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. You will be responsible for delivering high quality work, forming and maintaining valuable, long‑term relationships with our clients, and continually strengthening your technical and industry knowledge.
Key Responsibilities
Produce key project controls deliverables including detailed project schedules using MS Project, Oracle Primavera P6, or Smartsheets.
Prepare feasibility estimates, risk, forecasts, and What‑if scenario analysis.
Generate project cost reports and trend analysis.
Create comprehensive weekly and monthly project summary reports for stakeholders.
Conduct critical path analysis.
Prepare agendas, lead meetings, and track risk, actions, issues, decisions for the team.
Estimate budgets and analyze complex project data to deliver clear insights that support decision making.
Communicate with 3rd‑party vendors on behalf of the client to drive timelines.
Gain a general understanding of earned value analysis and PO management tools.
Maintain internal site tools such as site dashboards and deliverable trackers.
Align with cross‑functional client departments including Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering.
Qualifications
Bachelor’s Degree in Life Science, Engineering, Supply Chain, Construction Management or related discipline (or equivalent work experience).
Minimum 5 years of scheduling and/or project controls experience.
Proficiency with Microsoft Project, Primavera P6 and/or Smartsheet.
Willingness to be on‑site full‑time as client projects require.
Willingness to travel as required to support project and business needs.
Authorization to work in the United States on a full‑time basis.
Valid driver’s license; no violations.
Location & Travel Candidates should be located in or willing to relocate independently to Chicago, IL or Indianapolis, IN. This position may require significant travel to support project and business needs.
Benefits
Competitive salary based on experience.
Annual discretionary bonus.
Medical, dental, and vision insurance effective first day of employment.
401(k) plan with company match.
Paid time off and company paid holidays.
Company paid maternity and parental leave.
Continuing education assistance.
Core Services Examples of our core services within the life science space include capital project management (including project controls and scheduling), facility management & builds, tech transfers, validation life cycle (commissioning and qualification, process validation, computer system validation, etc.), GxP automated systems, due diligence & business strategy, quality, regulatory, & compliance.
Equal Opportunity Statement Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other protected characteristics. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
Benefits & Compensation Estimate Reasonable estimate of the current range: $50,000 USD – $240,000 USD.
Seniority Level Mid‑Senior level.
Employment Type Full‑time.
Job Function Management and Manufacturing.
Industries Technology, Information and Internet.
Referrals Referrals increase your chances of interviewing at Project Farma (PF) by 2x.
#J-18808-Ljbffr
If you are looking for a career accelerator, are driven by innovation, thrive in a fast‑paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.
About the Role As a Project Controls Engineering Consultant, you will work collaboratively with clients, vendors, contractors, and other Project Farma Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. You will be responsible for delivering high quality work, forming and maintaining valuable, long‑term relationships with our clients, and continually strengthening your technical and industry knowledge.
Key Responsibilities
Produce key project controls deliverables including detailed project schedules using MS Project, Oracle Primavera P6, or Smartsheets.
Prepare feasibility estimates, risk, forecasts, and What‑if scenario analysis.
Generate project cost reports and trend analysis.
Create comprehensive weekly and monthly project summary reports for stakeholders.
Conduct critical path analysis.
Prepare agendas, lead meetings, and track risk, actions, issues, decisions for the team.
Estimate budgets and analyze complex project data to deliver clear insights that support decision making.
Communicate with 3rd‑party vendors on behalf of the client to drive timelines.
Gain a general understanding of earned value analysis and PO management tools.
Maintain internal site tools such as site dashboards and deliverable trackers.
Align with cross‑functional client departments including Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering.
Qualifications
Bachelor’s Degree in Life Science, Engineering, Supply Chain, Construction Management or related discipline (or equivalent work experience).
Minimum 5 years of scheduling and/or project controls experience.
Proficiency with Microsoft Project, Primavera P6 and/or Smartsheet.
Willingness to be on‑site full‑time as client projects require.
Willingness to travel as required to support project and business needs.
Authorization to work in the United States on a full‑time basis.
Valid driver’s license; no violations.
Location & Travel Candidates should be located in or willing to relocate independently to Chicago, IL or Indianapolis, IN. This position may require significant travel to support project and business needs.
Benefits
Competitive salary based on experience.
Annual discretionary bonus.
Medical, dental, and vision insurance effective first day of employment.
401(k) plan with company match.
Paid time off and company paid holidays.
Company paid maternity and parental leave.
Continuing education assistance.
Core Services Examples of our core services within the life science space include capital project management (including project controls and scheduling), facility management & builds, tech transfers, validation life cycle (commissioning and qualification, process validation, computer system validation, etc.), GxP automated systems, due diligence & business strategy, quality, regulatory, & compliance.
Equal Opportunity Statement Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other protected characteristics. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
Benefits & Compensation Estimate Reasonable estimate of the current range: $50,000 USD – $240,000 USD.
Seniority Level Mid‑Senior level.
Employment Type Full‑time.
Job Function Management and Manufacturing.
Industries Technology, Information and Internet.
Referrals Referrals increase your chances of interviewing at Project Farma (PF) by 2x.
#J-18808-Ljbffr