Associate Director, Manufacturing

WHO WE ARE

RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.

THE ROSLINCT WAY

Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.

ACCELERATING YOUR FUTURE

The Associate Director of Manufacturing is responsible for leadership and oversight of cell therapy manufacturing. How You Will Make an Impact Ensure safety of manufacturing areas and work practices in alignment with site Health, Safety, and Environmental programs. Lead and develop a high-performing team to execute departmental objectives; ensure effective resource utilization through performance management and employee development. Provide leadership and direction to staff in alignment with cGMP requirements, and department goals. Partner with Scheduling and Supply Chain to support development and execution of production schedules and drive adherence within the functional area. Establish and monitor key performance indicators aligned with departmental goals; track and communicate performance metrics. Compliance/Training/Deviations Ensure staff are appropriately trained and qualified to perform assigned responsibilities. Oversee execution of the departmental training plan and ensure training materials are accurate and up to date. Ensure manufacturing instructions and batch records reflect current practices and are aligned with cGMP and company standards. Oversee timely completion of deviations, investigations, CAPAs, and Change Controls within the department. Quality & Regulatory Partnership Partner with Quality Assurance to support “right first time” execution and real-time process review. Maintain inspection readiness within assigned manufacturing areas. Review and approve manufacturing documentation and support implementation of process or documentation changes. Participate in regulatory inspections and client audits as a manufacturing subject matter expert. Continuous Improvement Identify and implement opportunities to improve manufacturing processes, efficiency, and compliance. Partner with cross-functional teams to troubleshoot operational issues and support timely resolution. Lead departmental projects and contribute to cross-functional initiatives, ensuring appropriate controls and follow-through. Leadership RoslinCT leaders motivate, inspire, build, and retain highly effective manufacturing team while managing for high performance and developing others. They are versatile learners and courageous decision makers. Create an environment of strong team spirit, timely and effective communications, sense of urgency, high motivation and inspire team to achieve goals in the immediate and longer term. Manage and administer people processes including selection, hiring, promotion, and compensation and provide training of personnel on company and department policies systems and processes. Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and exercising sound judgment in performing our jobs. Build a culture based on company values. What You Will Bring A highly organized work style that ensures timely execution of tasks. A mindset that ensures accurate results. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). Effective problem-solving capabilities. Strong oral and written communication skills. Qualifications Bachelor's degree in sciences or engineering discipline with a minimum of 10-15 years of industry experience or a master’s degree with a minimum of 8-10 years of industry experience. 8-10 years in managing direct reports or project teams. 5 years of direct experience in cell therapy GMP manufacturing facilities. Experience in GMP documentation and compliance. Ability to operate and thrive in a fast-paced, high-growth environment. Strong skills in change management. Excellent communication skills. Final compensation will be based on a variety of factors, including education, experience, technical expertise, specialized skill sets, market demand, internal equity, and business needs. At RoslinCT, we offer more than just competitive pay. Our comprehensive Total Rewards package is designed to support your health, financial well-being, and professional development throughout your career. Benefits include medical, dental, and vision insurance, educational assistance, a 401(k) program, and a variety of additional resources to help you thrive both personally and professionally.

OUR COMMITMENT

All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. RoslinCT is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics. #J-18808-Ljbffr RoslinCT US