Project / Validation Engineer

6 days ago


Houston, United States Project Farma (PF) Full time

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 Project Engineer. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. About the Role As a Project Engineer, you will provide hands‑on support and troubleshooting for clients navigating the engineering life cycle of cutting‑edge equipment and manufacturing processes. In your role, you will create alignment with cross‑functional client departments including, but not limited to, Validation, Manufacturing, Quality, Supply Chain, and Engineering. You will proactively identify and elevate roadblocks and utilize critical thinking skills and knowledge of problem‑solving skills to identify creative solutions to those problems and roadblocks. 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. About You You thrive in a fast‑paced environment. You are detail‑oriented and exhibit natural leadership qualities. 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 involvement in professional development and philanthropic opportunities. How Will You Spend Your Days As a Project Engineer Provide support and troubleshooting to clients regarding equipment and manufacturing processes. Perform due diligence on system and subject domains to generate high‑quality project deliverables. Author technical documents such as SOPs, requirements specifications, testing protocols, summary reports, etc. Execute system and process validation protocols using GxP best practices. Required Bachelor’s Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in CQV engineering, cGMP facility start‑up, project management and/or comparable military experience). Full‑time on‑site client presence. Willingness to travel as required to support project and business needs. 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. Benefits 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. 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 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 Entry level Employment Type Full‑time Job Function Quality Assurance Industries Technology, Information and Internet #J-18808-Ljbffr


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