Summer 2025 Engineer Intern/Co-op - Underground Construction & Tunneling
About Our Program:
Our co-op and intern program offers eligible college students an opportunity to alternate sessions of work and school with the added benefit of graduating with relevant work experience. Working in a variety of locations throughout the U.S. allows exposure to diverse work groups while providing invaluable leadership experience.
If relocation is required, it will be paid for by Traylor Bros. Interns may be assigned to any of our active projects or offices nationwide. This is opportunity is full-time requiring 40+ hours per week. This can be an internship or co-op position, depending on the university requirements of the student. This opportunity will last from approximately September - December 2024, but we can be flexible on start and end dates.
This position provides a variety of hands on experience and training needed to become an effective, well-rounded Civil Construction Engineer by exposure to both technical and administrative duties.
Open opportunities in for Underground Interns Fall 2024: CA, TX, VA
Typical responsibilities require applying critical engineering and management thinking which includes: estimating, design, scheduling, compliance review, procurement, surveying, production tracking, change order preparation, material testing and analysis, and cost report management. We are seeking professionals who are committed to safety, quality, and productivity.
THIS IS IN PERSON, ONSITE AT A JOB SITE INTERNSHIP! THIS IS NOT REMOTE!
Responsibilities Include:
Skills & Qualifications:
Physical Requirements:
EEO Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Required Skills
Required Experience
Minimum:
• High School Diploma or GED equivalent is required.
• Bachelor’s degree plus 2-4 years experience in Regulatory Affairs. In lieu of degree, 4+ years of experience in Regulatory Affairs will be considered.
• Minimum of 2 years of experience in Medical Device or related industry.
• Working knowledge with quality systems regulations and guidelines.
• Understanding of international submission requirements and regulatory framework, including how to comply with international standards and regulations.
• Must have the ability to develop clear, concise and timely oral and written reports, plus communicate tactfully with all levels of personnel.
• Working knowledge of medical devices, procedures and terminology.
• Proficiency with MS Office.
• Experience establishing and managing plans and timelines to achieve desired outcomes.
• Ability to solve problems through the application of critical thinking skills.
• Effective written and verbal communication skills, technical writing and editing skills.
• Ability to convey technical materials concisely to audiences of varying degrees of familiarity.
• Must be able to work in fast-paced, growing environment under management direction.
Preferred:
• 4+ yrs of experience in Medical Device industry or related field
• Bachelor’s degree
• International market submission experience
• High level of planning and organizational skills
• Effective research and analytical skills
• RAC certification
• SAP experience
• RIMS database experience
Other:
• Requires intense concentration to accurately assess compliance to applicable regulations for medical device manufacturers.
• The work is detail-oriented, often with multiple priorities
• The environment is deadline sensitive, with frequent high-pressure situations.
• Travel requirements are minimal.