Project Farma (PF)
Manager, Project Controls Engineering
Project Farma (PF), Raleigh, North Carolina, United States, 27601
Overview
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.
Responsibilities
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.
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 in support of 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.
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 (including Commissioning and Qualification, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.
Required
Bachelor’s Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
Minimum 3 years of scheduling and/or project controls experience.
Experience with Smartsheet, Microsoft Project, and/or Primavera P6 highly preferred.
Full-time on-site client presence.
Willingness to travel as required to support project and business needs.
Benefits
Competitive salary based on experience
Aggressive bonus structure
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
About Project Farma Project Farma is the leading advanced therapy technical operations consulting company in the life science industry. 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.
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.
Reasonable estimate of the current range: $50,000 USD - $240,000 USD
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.
Seniority level Mid-Senior level
Employment type Full-time
Job function Project Management and Information Technology
Industries Technology, Information and Internet
#J-18808-Ljbffr
Responsibilities
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.
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 in support of 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.
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 (including Commissioning and Qualification, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.
Required
Bachelor’s Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
Minimum 3 years of scheduling and/or project controls experience.
Experience with Smartsheet, Microsoft Project, and/or Primavera P6 highly preferred.
Full-time on-site client presence.
Willingness to travel as required to support project and business needs.
Benefits
Competitive salary based on experience
Aggressive bonus structure
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
About Project Farma Project Farma is the leading advanced therapy technical operations consulting company in the life science industry. 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.
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.
Reasonable estimate of the current range: $50,000 USD - $240,000 USD
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.
Seniority level Mid-Senior level
Employment type Full-time
Job function Project Management and Information Technology
Industries Technology, Information and Internet
#J-18808-Ljbffr