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.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Project Farma does not provide relocation assistance. Candidates should be located in (or willing to relocate independently to) Chicago, IL or Indianapolis, IN.

About you:
• You thrive in a fast-paced, and sometimes challenging environment.
• You are naturally detail-oriented, organized and exhibit natural leadership qualities.
• You enjoy engaging teams and mentoring others.
• You are comfortable acting as the sole Controls consultant for a client site.
• You work well in a team environment and can communicate to all levels of leadership.
• You are curious and ask questions to learn and understand our clients projects.
• You are currently or will live in the area where this job is posted.
• You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.

How will you spend your days as a Consultant, Project Controls Engineering?

• Produce key project controls deliverables, including:
  o Detailed project schedules using MS Project, Oracle Primavera P6, or Smartsheets.
  o Feasibility estimates, risks, forecasts, and What-if scenario analysis
  o Project cost reports and trend analysis
  o Comprehensive weekly and monthly project summary reports for stakeholders.
  o Critical Path Analysis
  o Preparing Agendas, leading meetings, tracking Risk, Actions, Issues, Decisions for the team.
  o Budget estimates
• Analyze complex project data and then deliver clear, articulate, and concise messages in a compelling manner to support decision making.
• Communicating with 3rd party vendors on behalf of the client to drive to their timelines.
• Gain a general understanding of Earned Value Analysis and PO management tools.
• Maintain internal site tools such as site dashboards, deliverable trackers, etc.
• Create alignment with cross-functional client departments, including Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering. (Moved to bottom).

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 (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:
• Bachelor's Degree in Life Science, Engineering, Supply Chain, Construction Management or related discipline (OR a combination of 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.

In return for your skills, knowledge, and passion, we offer a wide range of benefits including:
• Competitive salary based on experience
• Annual bonus (discretionary)
• Medical, Dental, and Vision insurance effective your first day of employment
• 401k Plan with company match
• Paid Time Off and Company Paid Holidays
• Company Paid Maternity and Parental Leave
• Continuing Education Assistance

Who are we?
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 is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$50,000-$240,000 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

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 QuestionForHR@precisionmedicinegrp.com.

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. 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.

---