Lead Production Floor Activities and Execute C&Q, Validation in a State-of-the-Art Facility
A fantastic opportunity awaits you to work on a cutting-edge fill-finish facility and the company's first stand-alone vaccine and biologics plant outside the US. As a Project Engineer, you will be responsible for leading/executing production floor-based activities, participating in a team of engineers, planning/executing C&Q, validation activities, designing/developing engineering studies, and providing technical input into quality notifications.
The ideal candidate will have a Bachelor's Degree or higher in a Science, Engineering, or other technical discipline, with prior related work experience in manufacturing, preferably GMP Setting. Strong knowledge of regulatory/core requirements is essential, along with proficiency in Microsoft Office and job-related computer applications. Effective communication, presentation, and interpersonal skills are also required to interface effectively with colleagues and external customers.
This role offers a unique blend of hands-on experience, collaboration, and technical expertise. If you're passionate about contributing to a world-class facility, we encourage you to apply.