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As a CQV Engineering Consultant at Precision Medicine Group, you will be at the forefront of innovation in patient-centered treatments. This role is designed for individuals who are passionate about delivering high-quality work and making a real impact in the life sciences industry. You will coordinate with cross-functional client departments, providing hands-on support throughout the engineering life cycle of cutting-edge equipment and manufacturing processes. Your responsibilities will include leading, overseeing, and executing client project initiatives, ensuring that team deliverables are completed in a timely and high-quality manner. In this fast-paced environment, you will develop technical documentation such as Standard Operating Procedures (SOPs), requirements specifications, testing protocols, and summary reports. You will also be responsible for building internal and external understanding and commitment to decisions through effective collaboration and presentation skills. Mentoring and coaching internal team members will be a key part of your role, as you help them develop industry best practices and project-driven technical skills. Additionally, you will support business development initiatives by maintaining professional networks and identifying client needs along with proposed support plans. Precision for Medicine, Manufacturing Solutions is committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. As a leader in the life sciences space, we offer a wide range of services including Capital Project Management, Facility Management, Tech Transfers, Validation Life Cycle, and Quality, Regulatory, & Compliance. This position is ideal for someone who thrives in a collaborative environment and is eager to contribute to the success of our partners and the patients we serve.