Intern, Engineering (High School Students ONLY)

Exela Pharma Sciences

Applications Closed

Posted 4 months ago

Internship

Lenoir, North Carolina

In Person

Smart Summary

The Engineering Intern will assist with equipment maintenance, support design modifications, and participate in process optimization efforts. They will also analyze production data and ensure compliance with industry standards.

This internship is designed for high school students interested in gaining hands-on experience in engineering within a pharmaceutical manufacturing setting. The role involves assisting with equipment maintenance, process improvement, and data analysis, requiring basic knowledge of engineering principles, strong problem-solving skills, and proficiency in Microsoft Office. Must be enrolled in high school (Junior or Senior preferred) and at least 18 years old.

Must Have Skills for ATS

Engineering Principles

Problem-Solving

Analytical Skills

Microsoft Office Suite

Teamwork

Communication Skills

Regulatory Standards

Manufacturing Processes

Quality Control

GMP

CAD Software

Process Optimization

Technical Documentation

Equipment Maintenance

Data Analysis

Root Cause Analysis

Job Description

Position Summary  

The Engineering Intern will support the engineering team in daily operations and projects within our pharmaceutical manufacturing plant. The intern will gain valuable hands-on experience in engineering design, process improvement, equipment maintenance, and safety protocols in a regulated environment. This role offers an excellent opportunity for those looking to apply their engineering knowledge in the pharmaceutical manufacturing sector.

*Must be enrolled in high school*

Job Responsibilities  

  • Assist with equipment maintenance and troubleshooting to ensure efficient plant operations.
  • Support the design and modification of plant systems, processes, and equipment.
  • Participate in process optimization efforts, including identifying inefficiencies and suggesting improvements.
  • Analyze production data and create reports for senior engineers and management.
  • Assist in ensuring compliance with industry standards and regulatory requirements (e.g., FDA, cGMP).
  • Contribute to root cause analysis and corrective actions for operational issues.
  • Participate in team meetings, offering ideas and support on current projects.
  • Collaborate with cross-functional teams, including quality control, operations, and maintenance departments.
  • Support the preparation of technical documentation, such as Standard Operating Procedures (SOPs) and engineering reports.

Experience Requirements  

  • Basic knowledge of engineering principles and practices.
  • Strong problem-solving and analytical skills.
  • Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
  • Ability to work independently and in a team environment.
  • Strong written and verbal communication skills.
  • Understanding of regulatory standards in the pharmaceutical industry (preferred but not required).
  • Previous internship or co-op experience in manufacturing or engineering is a plus.
  • Familiarity with CAD software (e.g., AutoCAD, SolidWorks).
  • Knowledge of manufacturing processes, such as batch production or continuous manufacturing.
  • Understanding of quality control processes and GMP (Good Manufacturing Practices).

 Education Requirements  

  • Must be enrolled in high school (Junior or Senior preferred)
  • Must be at least 18 years old

 EOE, including disability/vets 

Exela Pharma Sciences

Exela Pharma Sciences, a fast-growing specialty pharmaceutical company, focuses on developing, manufacturing and marketing generic and proprietary injectable and sterile ophthalmic products that keep the healthcare provider and patient in mind. Our goal is to deliver high quality, affordable products that make a difference in people’s lives, and also meet the needs of the healthcare providers that treat them. Exela targets the development and manufacturing of generic and proprietary injectable and sterile ophthalmic products with high barriers to market entry, via an Abbreviated New Drug Approval or 505(b)(2) regulatory pathway. We develop products that enhance the patient or provider experience such as easing the burden of administration, providing an improved safety profile, faster drug preparation, or reduce drug waste. In other words, we strive to improve patient outcomes while reducing overall health care costs.

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