2025 Summer Internship - Manufacturing Technical Services

The intern will collaborate with industry professionals to gain a deeper understanding of cleaning validation, process optimization, and regulatory compliance in a pharmaceutical manufacturing environment.

Key Responsibilities:

• Assist with cleaning validation projects, ensuring compliance with industry standards.
• Support process validation efforts, including data collection and analysis.
• Participate in process engineering investigations to troubleshoot and improve manufacturing operations.
• Collaborate with cross-functional teams to enhance manufacturing efficiency and compliance.
• Gain hands-on experience in pharmaceutical engineering principles and industry best practices.
• Document findings and support regulatory submissions as needed.

Qualifications & Skills:

• Currently pursuing or recently completed a degree in Pharmaceutical Engineering, Biomedical Engineering, or Pharmaceutical Manufacturing.
• Strong problem-solving and analytical skills.
• Ability to work effectively in a team-oriented environment.
• Excellent written and verbal communication skills.
• Knowledge of validation processes and regulatory compliance is a plus.

Benefits of the Internship:

• Gain real-world experience in pharmaceutical manufacturing and technical services.
• Work alongside experienced professionals in a fast-paced industry.
• Develop skills in process validation, cleaning validation, and engineering investigations.

Education:

• High School diploma or GED—Required
• Current full-time enrollment in an accredited college or university undergraduate or graduate program—Required
• Minimum cumulative GPA of 3.0—Required

Additional Requirements:

• Must be at least 18 years old.
• Must be legally authorized to work in the United States.
• Must commit to the full 10-12-week duration of the internship.

To be considered, candidates must meet all the above criteria.