Engineering Intern

STAQ Pharma; Columbus (OH); On-site; USD 24,796 - 34,440; Full time

Job summary

STAQ Pharma is seeking an Engineering Intern to support maintenance and cGMP system tasks with experienced engineers, contributing to various engineering projects and taking ownership of special tasks.

You will assist in applying engineering principles, manage project schedules, and execute validation activities on manufacturing equipment while collaborating with production operators and vendors.

Qualifications

• Current enrollment in an accredited Chemical, Mechanical, or Biomedical Engineering program.
• Sophomore, Junior, Senior, or graduate level.
• Excellent oral communication and technical writing skills.
• Microsoft Word and Excel experience.
• AutoCAD Microsoft Excel experience preferred.

Responsibilities

• Assist engineers in applying engineering principles, methods, and techniques.
• Lead assigned projects and manage schedules and daily progress.
• Execute validation activities on critical manufacturing equipment and utilities.
• Investigate and execute manufacturing process improvement projects.
• Create and update asset management documents related to maintenance and calibration.

Skills

Team player

Attention to detail

Manufacturing experience

Education

Engineering student (Chemical/Mechanical/Biomedical)

Sophomore/Junior/Senior or graduate level

Oral communication & technical writing

MS Word & Excel

AutoCAD experience preferred

Tools

AutoCAD

Microsoft Excel

Job description

Job Summary

The Engineering Intern is responsible for various maintenance and cGMP system tasks. Will have the opportunity to work closely with experienced engineers and contribute to various aspects of engineering projects. Should have the willingness to take on special projects and be naturally inclined to take ownership of tasks.

The Engineering Intern is responsible for various maintenance and cGMP system tasks. Will have the opportunity to work closely with experienced engineers and contribute to various aspects of engineering projects. Should have the willingness to take on special projects and be naturally inclined to take ownership of tasks.

Responsibilities

• Assist engineers in the application of principles, methods, and techniques of engineering.
• Serve as leader of assigned projects and manage a schedule and tracking daily progress
• Execute Validation activities on critical manufacturing equipment and utilities.
• Investigating and executing manufacturing process improvement projects
• Create and update asset management documents related to preventative maintenance and calibration requirements.
• Writing process, utilities, and validation procedures, evaluating test results, writing reports, and processing action to be taken with in the quality system.
• Driving practical knowledge of science and technology into all levels of the manufacturing organization for improved plant performance
• Lead cross functional teams to achieve improvement objectives, and monitor daily operations to find improvement opportunities
• Work with production operators, maintenance technicians and vendors staff on solving technical problems

Required Skills/Abilities

• Must be a team player and effectively collaborate with internal departments.
• Excellent attention to detail.
• Experience in a regulated manufacturing industry.
• Demonstrates ability to handle multiple responsibilities at any given time.

Education And Experience

• Current enrollment in an accredited Chemical, Mechanical, or Biomedical Engineering program. Other related Majors may be considered.
• Sophomore, Junior, Senior, or graduate level.
• Excellent oral communication and technical writing skills.
• Microsoft word and excel experience.
• AutoCAD Microsoft excel experience preferred. Current human resources and/or compensation credentials or certification preferred.

Physical Requirements

Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 15 pounds at times. The application window for this position is anticipated to be open at least 25 days