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Technical Operations Intern

Nevakar Inc.
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Internship Title: Technical Operations Intern

Department/Team: Technical Operations

Internship Duration: June 8, 2026 – August 14, 2026 (10 weeks)

Location: Bridgewater, NJ (onsite)

 

Role Overview:

Nevakar Injectables is currently seeking a talented and innovative intern to join our Technical Operations Department located at Bridgewater, New Jersey. As an intern, you will be engaged in the technical development of sterile injectable projects, that include supporting activities relating to strategic planning, execution and verification of design history file documents for combination drug products, and cross-functional collaborative activities with quality, R&D, and regulatory affairs. Mentorship experience would expose the intern to fundamental design history principles, technical documentation for GMP activities and robust understanding of sterile injectable drug products.

 

Responsibilities:

  • Author documents to support design history file of combination drug products
  • Collaborate with R&D in identifying optimal parameters relevant to manufacturing sterile injectables products
  • Perform data analysis, verification, and interpretation
  • Conduct literature search for assigned project
  • Create database of CDMOs for sterile injectable products

 

Learning Objectives:

  • Understand the requirements of design history file of combination products
  • Understand the principles of GMP manufacturing
  • Immerse in bridging the understanding between R&D laboratory-generated knowledge to manufacturing in commercial scale of sterile injectables
  • Gain collaborative experience through interaction with CDMOs on project-related activities

 

Qualifications: 

  • Candidates must be enrolled in either a Bachelors (within 3rd year or higher), Masters, or Doctoral program in Pharmaceutical Science-, Material Science- or Chemical Engineering-related field.
  • Successful candidates must have taken some courses in chemistry, pharmaceutical sciences, chemical engineering, or other relevant courses. Previous experience in pharmaceutical industry or scientific research is a plus.
  • Must be able to work full-time (40 hours/week) during the duration of internship program
  • Should be able to commute on site (Bridgewater, New Jersey) for the duration of internship program
  • Required GPA of 3.5 and above