Senior Project Controls Engineer

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.

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.

• Produce key project controls deliverables, including detailed project schedules using MS Project, Oracle Primavera P6, or Smartsheets; feasibility estimates, risks, forecasts, and what‑if scenario analysis; project cost reports and trend analysis; comprehensive weekly and monthly project summary reports for stakeholders; critical path analysis; preparing agendas, leading meetings, tracking risk, actions, issues, decisions for the team; budget estimates.
• Analyze complex project data and deliver clear, articulate, and concise messages in a compelling manner to support decision making.
• Communicate with third‑party vendors on behalf of the client to drive their timelines.
• Gain a general understanding of Earned Value Analysis and PO management tools.
• Maintain internal site tools such as site dashboards and deliverable trackers.
• Create alignment with cross‑functional client departments, including Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering.

• Bachelor’s Degree in Life Science, Engineering, Supply Chain, Construction Management or related discipline (or equivalent work experience in Project Controls, cGMP facility start‑up, project management and/or comparable military experience).
• Minimum 5 years of scheduling and/or project controls experience.
• Experience with Microsoft Project, Primavera P6 and/or Smartsheet necessary.
• Willing to be on‑site full‑time as client projects require.
• Willingness to travel as required to support project and business needs.

Reasonable estimate of the current range: $50,000 - $240,000 USD

• Competitive salary based on experience
• Annual bonus (discretionary)
• Medical, Dental, and Vision insurance effective your 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

As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next‑generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground‑breaking treatments and solutions.

We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams’ and partners’ long‑term success.

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 characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionF