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.
Seniority level
Internship
Employment type
Full-time
Job function
Management and Manufacturing
Industries
Pharmaceutical Manufacturing
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