As the Director of CQV for our Life Sciences North America (LSNA) team, you'll be at the forefront of delivering innovative solutions and ensuring the seamless manufacturing of life-changing GMP products. This is your chance to join the #1 Global Engineering, Procurement, Construction, and Validation organization and partner with clients that are transforming lives through their groundbreaking products. We are seeking a leader in either Conshohocken, PA, Cary, NC or Cincinnati, OH who thrives on collaboration, sets high expectations, and isn’t afraid to challenge the status quo. If you’re passionate about driving excellence and innovation in CQV solutions, this role is your opportunity to shine. What You’ll Do: • Lead cross-functional teams in executing commissioning, qualification, validation, and process transfer activities to achieve company and client goals. • Champion our mission and core values, inspiring a high-performance CQV team of 90+ professionals to excel. • Spearhead strategies that drive growth, optimize processes, and elevate our CQV operations. • Build and strengthen relationships with clients and partners, serving as a trusted advisor and industry thought leader. • Take charge of business development initiatives, crafting innovative proposals and expanding our reach in the life sciences sector. • Mentor and empower your team, fostering an environment of accountability, collaboration, and growth. • Represent the organization at industry conferences, showcasing our expertise and amplifying our presence in the life sciences community. • Ensure ongoing compliance with ever-evolving regulatory standards and implement risk management best practices. Please note: The closing date for this opportunity is COB May 21, 2025. • A visionary people leader with a BS/MS in Engineering, Technical, or Life Science disciplines and a track record of building and managing high-performing teams. • Armed with 5+ years of leadership experience and 10+ years of CQV expertise in the biopharmaceutical industry, with in-depth technical knowledge and project management mastery. • A strategic thinker with business acumen, sales/proposal experience with comfort selling to clients, stellar communication skills, and a results-driven mindset. • Engineering knowledge of, and experience with, manufacturing equipment, process equipment, HVAC, utilities, instrumentation, controls, and automation to support clients • Adept at navigating regulatory landscapes, including US FDA (21 CFR 210, 211, 810) and EU EMEA guidelines, and experienced with industry standards like ISPE Baseline Guide 5, GAMP V, and ASTM E2500. • Flexible and ability to travel. #LifeSciences, #Bio/Pharma, #EPCMV, #globallifescience #LI-SH1 Jacobs is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, religion, creed, color, national origin, ancestry, sex (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, medical condition, marital or domestic partner status, sexual orientation, gender, gender identity, gender expression and transgender status, mental disability or physical disability, genetic information, military or veteran status, citizenship, low-income status or any other status or characteristic protected by applicable law. Learn more about your rights under Federal EEO laws and supplemental language.