The Engineering Intern will provide support on capital projects and continuous improvement initiatives at our facility located in Wilmington, Ohio. The Intern will assist with the execution of engineering tasks under the supervision and direction of the Engineering Services department. The Intern will be tasked with reviewing mechanical system drawings, field verification new and existing equipment, reviewing equipment files from completed projects, supporting the documentation of project implementation, and data collection and analysis from control systems.
The Intern will be provided with opportunities for training and exposure to pharmaceutical HVAC, electrical, water purification, steam, compressed process gases, waste treatment, and pharmaceutical process system design practices. The Intern will support continuous improvement initiatives by performing detailed engineering studies of utility systems to determine existing utilization, excess capacity, and opportunities for efficiency improvement.
Responsibilities
Review mechanical system diagrams and construction drawings throughout the design and implementation of capital projects
Perform field verification of new equipment, mechanical drawings, and construction documentation after the implementation of capital projects
Compile and review project turnover documentation packages
Support the completion of project documentation and system commissioning, including the completion of Engineering Checklists and the generation of cGMP forms
Support review and creation of equipment files
Support the identification and implementation of continuous improvement projects, primarily focused on energy efficiency and waste reduction
Manage the implementation of departmental projects as delegated by Engineering Services
Perform all documentation in accordance with cGMP, GEP and Regulatory requirements
Qualifications
Currently enrolled in an educational program working towards a degree in Engineering
Sophomore-Senior status in Mechanical Engineering or Chemical Engineering preferred
Proficient in Word, Excel
Excellent data analysis and problem-solving skills
Fast learner, self-motivated, able to prioritize many tasks and provide feedback on workload
Ability to communicate and comfortably interact with employees at all levels of the organization and across different department functions
Excellent written and verbal communication skills
Knowledge of cGMP documentation practices and system commissioning preferred
Previous experience in the Pharmaceutical industry or other relevant cGMP industry preferred