CQV Engineering Consultant Boston, Massachusetts, United States

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 CQV Engineering Consultant. 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 CQV Engineering Consultant, you will coordinate with cross functional client departments providing hands‑on support in navigating the engineering life cycle of cutting‑edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high‑quality fashion. About you: You thrive in a fast‑paced environment. You are detail‑oriented and exhibit natural leadership qualities. You enjoy engaging teams and mentoring others. 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 CQV Engineering Consultant? Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc. Build internal and external understanding, buy‑in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills. Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills. Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way. Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan. Examples of our core services within the life science space: 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, or related discipline and/or comparable military experience. A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience. Willingness to travel as required to support project and business needs. 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. In return for your skills, knowledge, and passion, we offer a wide range of benefits including: 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 Who are we? We are Project Farma, 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. Reasonable estimate of the compensation range for this role: $50,000 - $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. We comply with the federal, state, and local laws for disability accommodation. 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. #J-18808-Ljbffr