Engineering Intern

Mallinckrodt Pharmaceuticals • Horsham, PA

43d • Onsite

About The Position

Keenova is a leading pharmaceutical company dedicated to developing and manufacturing therapies that improve patient lives. We are committed to the highest standards of quality, safety, and regulatory compliance in everything we do. Keenova is seeking a motivated Engineering Intern to join our Facilities team for Summer 2026. This internship offers hands-on exposure to pharmaceutical systems in a highly regulated GMP environment. The intern will support Engineering and Validation activities, including installation, qualification, and documentation of systems such as Environmental chambers, Autoclaves, Parts washers, Fermentation equipment, and control systems for process equipment. This will include assisting with project management, installation, document preparation, assisting with set up for execution of qualification protocols, compiling data to summarize qualification efforts, and contributing to site goals related to Facilities and Validation objectives. This is an excellent opportunity for students pursuing degrees in life sciences, Engineering, chemistry, biology, or related fields to gain practical industry experience. The Engineering Intern supports projects by compiling data, assisting with various qualifications, reviewing and compiling documents, and following up on action items related to existing projects.

Requirements

• Must be currently enrolled in an undergraduate or graduate program.
• Actively enrolled in a relevant field of study such as Engineering or Project Management
• Skills/Qualifications
• Knowledge of MS Office Suite (MS Word, MS Excel, MS PowerPoint, MS Visio)
• Engineering or other technical coursework
• Strong written and oral communication skills
• Critical thinking
• Effective communication and organizational skills
• Attention to detail

Nice To Haves

• Knowledge of GMP Preferred (Good Manufacturing Practices)

Responsibilities

• Provide project management support related to change management, drawing updates, and scheduling.
• Assist with documentation tasks, validation studies and reports to support timely project completion in compliance with cGMP, FDA regulations, and company SOPs.
• Provide administrative support during departmental meetings as required.
• Support departmental staff in preparation of qualification studies and general facility activities.
• Contribute to current process improvement efforts.
• Perform other duties as assigned by the Validation and Facilities team.

What This Job Offers

• Career Level: Intern
• Education Level: No Education Listed