Looking to kickstart your career in Regulatory Affairs? Aurobindo Pharma is offering a 6-month internship in Hyderabad. Walk-In on 29th Sept 2024. Apply by 27th Sept 2024. MPharm freshers welcome.
Aurobindo Pharma Job Overview
| Job Role | Global Regulatory Affairs Intern |
|---|---|
| Qualification | M.Pharm Fresher (Pharmaceutics, Regulatory Affairs, PA&QA) |
| Company Website | www.aurobindo.com |
| Experience | Fresher |
| Salary | ₹12,000/month |
| Job Type | Internship (6 months) |
| Location | Hyderabad (Miyapur, Bachupally) |
| Skills/Requirements | CMC document review, Knowledge of eCTD, Learning agility |
About Aurobindo Pharma
Aurobindo Pharma is one of the top pharmaceutical companies in India, exporting to over 150 countries worldwide. With several international regulatory approvals, the company is known for its robust R&D initiatives, rapid filing of Drug Master Files (DMFs), and formulation dossiers.
Role and Responsibilities
As a Global Regulatory Affairs Intern, you will:
- Help with the assignment of regulatory filings, including their preparation, review, and compilation.
- Acquire practical experience in examining Chemistry, Manufacturing, and Controls (CMC) documentation pertaining to oral dosage forms, including liquid and solid.
- Learn how to use the electronic Common Technical Document (eCTD) system with ease.
This role is a great opportunity for M.Pharm freshers to gain valuable industry experience and global exposure.
Internship Highlights
- Work closely with leadership: Gain mentorship and guidance from experienced professionals.
- Global exposure: Experience the international aspects of regulatory affairs.
- Hands-on learning: In-depth understanding of CMC documentation for pharmaceutical products.
Preferred Candidate Profile
To be considered for this role, you should be:
- A M.Pharm Fresher with a focus on Pharmaceutics, Regulatory Affairs, Pharmaceutical Chemistry, or PA&QA.
- Eager to learn and adapt, with strong learning agility.
Aurobindo Pharma Walk-In Details
Date: 29th September 2024 (Sunday)
Time: 10:00 AM to 12:00 Noon
Location: Aurobindo Pharma Ltd Research Centre-1 (APLRC1), Bachupally, Miyapur, Hyderabad
Important Dates:
- Apply by: 27th September 2024
- Start Date: 3rd October 2024
How to Apply
- Click the Apply Link: Begin your application process by clicking the provided link on the official website.
- Complete the Application: Fill in your details and submit the required documents before the 27th of September 2024.
- Prepare for the Walk-In: Attend the walk-in interview on 29th September at the specified location.
Resume Keywords for Global Regulatory Affairs Intern at Aurobindo Pharma
Incorporating the right keywords into your resume is crucial for passing through Applicant Tracking Systems (ATS) and standing out during manual reviews. Here are tailored resume keywords for the Global Regulatory Affairs Intern role at Aurobindo Pharma, along with suggestions on where to insert them:
1. Resume Keywords
These keywords are aligned with the job description and should be sprinkled throughout your resume in the following sections:
- Objective/Summary
- Work Experience/Internships
- Skills
- Projects
- Education
| Category | Keywords to Use |
|---|---|
| Regulatory Affairs | Regulatory Submissions, eCTD, Regulatory Filings, Global Compliance, CMC Documentation |
| Pharma/Science Skills | Solid Oral Dosage Forms, Liquid Oral Dosage Forms, M.Pharm, Pharmaceutics, PA&QA |
| Technical Skills | Document Review, Drug Master Files (DMF), ANDA, FDA Submissions, Dossier Preparation |
| Software/Tools | eCTD Software, Microsoft Office, Data Entry, Regulatory Software |
| Soft Skills | Learning Agility, Attention to Detail, Time Management, Critical Thinking |
| Industry Terms | Pharmaceutical Chemistry, Regulatory Affairs, GMP (Good Manufacturing Practices) |
| Communication Skills | Report Writing, Technical Documentation, Team Collaboration |
Where to Insert Them:
- Objective/Summary Section:
- Example: “Detailed Oriented Graduate of M.Pharm program with practical expertise in regulatory filings and CMC documentation for both liquid and solid oral dosage forms. competent in regulatory filings for international markets and eCTD systems.”
- Skills Section:
- List specific technical and industry skills like:
- Regulatory Submissions (eCTD), CMC Documentation, Solid and Liquid Dosage Forms, Learning Agility, GMP Knowledge
- Experience/Projects Section:
- If you have any internship experience, even from academia, mention relevant terms like:
- “Developed expertise in FDA and international regulatory submissions by preparing and reviewing CMC documentation for solid oral dosage forms.”
- For academic projects:
- “Worked on a formulation project involving regulatory submission requirements for liquid oral dosage forms.”
- Education Section:
- You can mention coursework or academic experience with regulatory affairs, formulation, and CMC in your degree:
- M.Pharm in Pharmaceutics with coursework in Regulatory Affairs, CMC, and Pharmaceutical Chemistry.
Interview Tips for the Global Regulatory Affairs Intern Role
Preparing for the interview at Aurobindo Pharma involves a mix of technical and behavioral readiness. The following advice will help you succeed:
1. Understand the Role
- Familiarize yourself with the basics of regulatory filings, especially the eCTD system, and CMC documentation for pharmaceutical products. Research on how these documents play a role in regulatory compliance for solid and liquid oral dosage forms.
- An example question would be, “Can you explain the significance of CMC documentation in the process of approving drugs?”
2. Research the Company
- Know about Aurobindo Pharma’s global presence, their regulatory approvals, and key markets. Highlight any specific knowledge of the company’s work in regulatory filings for international markets, including FDA or EU GMP.
- Example Question: “What do you know about Aurobindo Pharma’s regulatory filing process?”
3. Brush Up on Pharma Regulations
- Be ready to discuss major regulatory agencies (e.g., FDA, EU GMP, MHRA), and their requirements. Understand key terms like ANDA (Abbreviated New Drug Applications) and DMF (Drug Master File).
- Example Question: “What are the key regulatory bodies in the pharmaceutical industry, and what role do they play?”
4. Demonstrate Soft Skills
- Emphasize your learning agility, attention to detail, and time management. Regulatory affairs require meticulous work and a quick adaptation to changing regulations.
- Example Question: “How do you ensure accuracy when reviewing large volumes of regulatory documents?”
5. Technical Skills Demonstration
- If you have prior experience with eCTD software or handling regulatory documentation (even through academic projects), share specific examples.
- Example Question: “What systems or technologies have you utilized for regulatory submissions, and how have you used them in a project?”
6. Ask Insightful Questions
- Prepare questions that show your interest in learning and growing within the regulatory field, such as:
- “What opportunities are available for interns to learn more about global regulatory processes at Aurobindo?”
- “Can you describe a typical day in the Regulatory Affairs department?”
Final Note:
Make sure to practice mock interviews, especially on technical topics like CMC documentation and regulatory submissions. It’s also important to demonstrate your enthusiasm for working in a highly regulated field like pharmaceuticals.
Frequently Asked Questions (FAQs)
Q1: Who is eligible to apply for this internship?
- M.Pharm freshers specializing in Pharmaceutics, Regulatory Affairs, Pharmaceutical Chemistry, or PA&QA are eligible to apply.
Q2: What is the duration of the internship?
- The internship will last for 6 months, starting from 3rd October 2024.
Q3: Is prior experience required?
- No, this role is specifically for freshers with no prior experience.
Q4: What are the walk-in details?
- The walk-in interview will take place on 29th September 2024, from 10:00 AM to 12 Noon at Aurobindo Pharma Ltd Research Centre-1 (APLRC1), Bachupally, Miyapur, Hyderabad.
Q5: Will I get a full-time role after the internship?
- While this is a 6-month internship, outstanding performance could lead to potential full-time opportunities within the company.
Disclaimer:
This post is for informational purposes only, and no fees are charged to apply for this role. All the information provided here has been sourced from official company websites and reliable resources.
Also Check:
2 thoughts on “Aurobindo Pharma: Global Regulatory Affairs Internship (Paid)”