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Manufacturing Intern
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Job Description
Manufacturing Intern | Sterling Pharma Solutions
The Tone:
This is a paid 11-week internship at Sterling Pharma Solutions, located in Germantown, WI. Sterling Pharma Solutions is a global contract development and manufacturing organization (CDMO) with over 50 years of experience in developing and manufacturing Active Pharmaceutical Ingredients (APIs). This program offers hands-on experience, allowing interns to build upon classroom knowledge by contributing to a team dedicated to developing life-saving drugs. Interns will learn GMP fundamentals and techniques directly from industry leaders.
The TL;DR
• Role: Internship
• Type: Temporary
• Location: Germantown, WI (On-site)
• Mission: Contribute to GMP manufacturing processes, documentation, and improvement initiatives to support the development of pharmaceutical products.
• Tech Stack: Microsoft Office applications (Outlook, PowerPoint, Word, Excel)
What You’ll Actually Do
• Batch Record Management: Stage, meticulously review, and close batch records while accurately tracking their status within a GMP manufacturing setting.
• Material Labeling: Request and apply labels to materials, ensuring correct identification and compliance with procedural requirements.
• Process Exposure: Gain direct exposure to various stages of batch processes across different manufacturing bays.
• Improvement Contribution: Actively review current processes and contribute to improvement initiatives within manufacturing Bays.
• Documentation Understanding: Become familiar with Standard Operating Procedures (SOPs), work instructions, and other critical GMP documentation.
The Must-Haves
• Background: Minimum qualification: Bachelor’s Degree. Career level: Early Career. Currently enrolled as a Sophomore level or higher in a 2 or 4-year college or university, pursuing a Bachelor’s degree in Chemistry, Biology with a Chemistry Minor, or Pharmaceutical Sciences.
• Experience: No specific years required.
• Skills: Excellent verbal and written communication and documentation skills, strong detail orientation and organizational skills, excellent problem-solving and basic trouble-shooting ability, ability to handle multiple tasks effectively, competency with IT systems and Microsoft Office applications (Outlook, PowerPoint, Word, Excel). Must maintain a cumulative GPA of 2.75 or higher.
• Bonus: Awareness or prior work experience in a GMP environment is preferred.
