Job Description
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.
Qualifications
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.
