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Intern, R&D

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Aurobindo Pharma USA, Inc.

2mo ago

  • Internship
    Full-time
    Summer Internship
  • Research & Development
    Healthcare

AI generated summary

  • You should be enrolled in a Pharmaceutics program, knowledgeable in pharmaceutics and ANDA filing, and possess strong communication skills. Experience in formulation development is preferred.
  • You will develop and file generic drug dosage forms, utilize FBD, compression, and encapsulation techniques, and manage projects from bench-top to large-scale manufacturing of submission batches.

Requirements

  • Knowledge of pharmaceutics, pharmacokinetics and process scale-up
  • Understanding of the ANDA (and preferably NDA) filing process in line with QbD elements in generic product development
  • Ability to work and collaborate in a team environment
  • Excellent spoken and written communication skills
  • Must be currently enrolled in a Bachelor's or Master's degree program in Pharmaceutics or a related field
  • Experience in formulation development and process development is preferred
  • Experience in the generic drug industry with ANDA filing and/or working with DEA controlled drug substances and relevant regulations is a plus
  • While performing the duties of this job the employee is required to:
  • Stand, sit; talk, hear, and use hands and fingers to operate a computer and telephone keyboard reach, stoop kneel to install computer equipment
  • Specific vision abilities required by this job include close vision requirements due to computer work
  • Light to moderate lifting is required
  • Moderate noise (i.e. business office with computers, phone, and printers, light traffic).
  • Ability to sit at a computer terminal for an extended period of time
  • Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body.
  • Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
  • No Additional Requirements
  • Blood/Fluid Exposure Risk: Category III: Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.

Responsibilities

  • Develop and file generic drug dosage forms (orals/liquids)
  • Develop products using FBD, Compression and Encapsulation
  • Complete projects from bench-top stage to large scale manufacture of submission batches

FAQs

What is the nature of the internship position?

The internship position is focused on R&D in generic pharmaceutical product development and is a temporary, hands-on role.

What qualifications are required to apply for this internship?

Candidates must be currently enrolled in a Bachelor's or Master's degree program in Pharmaceutics or a related field.

Is prior experience in the pharmaceutical industry necessary?

While it is preferred, prior experience in formulation development, process development, or the generic drug industry with ANDA filing and/or working with DEA controlled substances is not a strict requirement.

What kind of projects will the intern be working on?

The intern will be involved in developing and filing generic drug dosage forms, working on projects from bench-top stage to large-scale manufacture of submission batches.

Are there any physical requirements for this position?

Yes, the position requires light to moderate lifting and involves sedentary work, including sitting at a computer for extended periods.

Will the intern receive training in the ANDA filing process?

Yes, understanding the ANDA filing process in line with Quality by Design (QbD) elements is part of the internship responsibilities.

Is there an opportunity for full-time employment after the internship?

The job description does not specify opportunities for full-time employment post-internship; it is designated as a temporary position.

What skills are emphasized for this role?

Strong knowledge of pharmaceutics, pharmacokinetics, process scale-up, and excellent spoken and written communication skills are emphasized for this role.

What is the work environment like?

The work environment is an office setting that may involve moderate noise from computers, phones, and printers, with light traffic.

How does Aurobindo Pharma USA, Inc. approach equal opportunity employment?

Aurobindo Pharma USA, Inc. provides equal employment opportunities and prohibits discrimination and harassment of any type, ensuring compliance with federal, state, and local laws.

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Aurobindo Pharma USA, Inc.

Committed to Healthier Life!

Manufacturing & Electronics
Industry
1001-5000
Employees
1994
Founded Year

Mission & Purpose

Aurobindo USA is committed to delivering a broad portfolio of quality, affordable generic pharmaceuticals to pharmacists and patients. Since its first US ANDA approval in 2004, Aurobindo has expanded its portfolio to include more than 150 product families, representing a wide range of therapeutic categories. Aurobindo has been recognized as the fastest growing pharmaceutical company in 2012,* and in early 2013, thanks to the ongoing support of our customers, became one of the top 10 pharmaceutical companies, brand or generic, in terms of total prescriptions dispensed.**