A leading biopharmaceutical company in Boca Raton, FL, is seeking a Senior Project Engineer to provide engineering and project management support. Responsibilities include managing engineering projects, developing commissioning plans, and assisting in regulatory documentation for FDA submissions. The ideal candidate has a minimum of 10 years in a cGMP environment, possesses strong technical writing skills, and can thrive in a high-pressure setting. Competitive benefits package offered, including 401K and health insurance.
Qualifications
Minimum of 10 years of engineering experience in a cGMP Pharmaceutical/Biological manufacturing environment.
Ability to work in high-pressure, deadline-driven environment.
Must possess exceptional organizational and communication skills.
Responsibilities
Manage engineering projects by planning and tracking cross-functional teams.
Develop commissioning plans for process and utility systems.
Assist in writing regulatory documents for FDA submissions.
Skills
Project management
Problem-solving
Technical writing
Analytical skills
Time management
Tools
Microsoft Office
Project management software
Job description
A leading biopharmaceutical company in Boca Raton, FL, is seeking a Senior Project Engineer to provide engineering and project management support. Responsibilities include managing engineering projects, developing commissioning plans, and assisting in regulatory documentation for FDA submissions. The ideal candidate has a minimum of 10 years in a cGMP environment, possesses strong technical writing skills, and can thrive in a high-pressure setting. Competitive benefits package offered, including 401K and health insurance.