Operations Internship – Labeling Process & Formulation Laboratory

Cordis, in partnership with Selution, specializes in the development of advanced drug device combination products for healthcare. The Operations Intern will support daily activities in the Labeling Process and Formulation Laboratory, ensuring compliance with quality standards and regulatory requirements.

What you'll do:

• Assist with the preparation, verification, and issuance of product labels in accordance with approved procedures and regulatory requirements
• Support label reconciliation, inspection, and documentation activities
• Verify label accuracy, including product information, lot numbers, expiration dates, and barcode readability
• Participate in label change control and document revision processes
• Help maintain compliance with Good Documentation Practices (GDP) and Standard Operating Procedures (SOPs)
• Assist laboratory personnel in preparing formulations, solutions, and materials according to established procedures
• Support laboratory testing, sample preparation, and data collection activities
• Maintain laboratory equipment cleanliness, calibration records, and inventory of chemicals and consumables
• Record experimental observations and maintain accurate laboratory documentation
• Follow laboratory safety protocols and Good Laboratory Practices (GLP)
• Support production documentation, and quality records
• Collaborate with Manufacturing, Quality Assurance, Regulatory Affairs, and Engineering teams

What they're looking for:

• Currently pursuing a bachelor's degree in a related scientific discipline
• Strong interest in medical device manufacturing and regulated industries
• Basic understanding of laboratory practices and manufacturing operations
• Familiarity with Microsoft Office Suite (Excel, Word, PowerPoint)
• Excellent organizational, analytical, and communication skills
• Ability to work independently and collaboratively in a team environment
• High attention to detail and commitment to quality and compliance
• Knowledge of ISO 13485, FDA Quality System Regulation (21 CFR Part 820), or Good Manufacturing Practices (GMP)
• Experience with laboratory techniques or manufacturing environments through coursework or previous internships
• Exposure to Lean Manufacturing or Six Sigma concepts is an advantage