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"Regulatory Affairs Intern Hiring at ArtiXio | Paid Remote Internship for Pharmacy & Life Sciences"
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"Regulatory Affairs Intern Hiring at ArtiXio – Paid Remote Internship"
(Regulatory Affairs Intern Hiring at ArtiXio)
Introduction
If you are a pharmacy or life sciences student looking to start your career in Regulatory Affairs, getting real-world exposure is more important than theoretical knowledge alone. Regulatory Affairs is a highly specialized and globally relevant domain, and early hands-on experience can make a huge difference in long-term career growth.
ArtiXio has announced an excellent opportunity for freshers and students by opening applications for a Regulatory Affairs Intern (Paid – Remote) role. This internship is designed for candidates who want practical exposure to global pharmaceutical and medical device regulations, CTD/eCTD dossiers, and regulatory consulting projects.
About the Company – ArtiXio
ArtiXio is a fast-growing life sciences regulatory and compliance consulting startup that supports pharmaceutical, medical device, biologics, and nutraceutical companies across global markets. The company focuses on providing end-to-end regulatory solutions, regulatory intelligence, and compliance consulting to help clients navigate complex global regulatory frameworks.
Company Overview
Company Name: ArtiXio
Industry: Life Sciences Consulting & Regulatory Affairs
Headquarters: Hyderabad, Telangana, India
Founded: 2023
Employees: 20+ regulatory professionals and consultants
ArtiXio works in a startup-driven environment where interns get direct exposure to live global projects, making it an ideal place to start a Regulatory Affairs career.
Job Overview Summary
The Regulatory Affairs Intern role at ArtiXio is a paid, fully remote internship based out of Hyderabad. Interns will work closely with experienced regulatory consultants on active client projects involving pharmaceuticals, medical devices, biologics, and nutraceuticals.
This internship is best suited for students or fresh graduates who want hands-on exposure to global regulatory submissions, dossier management, and regulatory research instead of routine academic internships.
Vacancy Details
Job Title: Regulatory Affairs Intern
Company: ArtiXio
Location: Remote (Base: Hyderabad, Telangana)
Internship Type: Paid Internship
Work Mode: Fully Remote
Industry: Pharmaceutical & Life Sciences Consulting
Experience Required: Fresher / Student
Job Role Explanation – Regulatory Affairs Intern
As a Regulatory Affairs Intern at ArtiXio, you will be actively involved in real regulatory projects. Unlike traditional internships, this role focuses on practical regulatory work aligned with industry standards.
Interns will gain exposure to:
Global pharmaceutical regulations
Medical device regulatory pathways
Regulatory submissions and lifecycle management
Consulting-based regulatory strategy development
Responsibilities Explanation
During the internship, you will support the regulatory team in multiple areas, including:
Researching and analyzing global regulatory requirements for pharma, medical devices, biologics, and nutraceuticals
Assisting in the preparation, review, and maintenance of CTD and eCTD dossiers
Supporting regulatory submissions, variations, renewals, and lifecycle activities
Tracking global regulatory updates, approvals, and policy changes
Maintaining regulatory databases and documentation records
Preparing regulatory reports, client presentations, and internal knowledge materials
Working closely with senior regulatory consultants on live client assignments
This hands-on exposure helps interns understand how regulatory decisions impact real pharmaceutical products.
Eligibility Criteria (Official)
This Regulatory Affairs Internship is suitable for candidates who meet the following criteria:
Pursuing or completed B.Pharm, M.Pharm, MSc (Life Sciences), Biotechnology, or Regulatory Affairs
Strong interest in global regulatory frameworks (USFDA, EMA, CDSCO, ICH)
Willingness to learn regulatory documentation and compliance processes
Comfortable with regulatory research and data handling
Skills Required
To succeed in this role, candidates should have:
Basic understanding of pharmaceutical and medical device regulations
Good documentation and report-writing skills
Proficiency in MS Word, Excel, and PowerPoint
Strong attention to detail and compliance mindset
Good written and verbal communication skills
Ability to work independently in a remote startup environment
Curiosity and willingness to learn regulatory consulting practices
Salary / Stipend Estimate
Estimated Stipend: ₹15,000 – ₹25,000 per month
This is a paid Regulatory Affairs internship, which is rare in the pharma regulatory domain, especially for freshers.
Interview Details
Interview Mode: Online (Virtual)
Selection Process:
Resume Shortlisting
Technical & Regulatory Discussion
Final HR Interaction
Candidates with strong regulatory fundamentals and learning intent will be preferred.
Required Documents
Applicants should keep the following documents ready:
Updated Resume (Regulatory-focused preferred)
Educational Certificates / Mark Sheets
Government ID Proof
Internship / Training Certificates (if available)
Cover Email highlighting interest in Regulatory Affairs
FAQs – Regulatory Affairs Internship at ArtiXio
Q1. Is this a paid Regulatory Affairs internship? Yes, ArtiXio offers a paid internship with a monthly stipend.
Q2. Is the internship fully remote? Yes, this is a completely remote internship.
Q3. Can freshers apply for this internship? Yes, students and fresh graduates from pharmacy and life sciences backgrounds can apply.
Q4. Is there a PPO opportunity after an internship? Yes, high-performing interns may receive a Pre-Placement Offer (PPO).
Q5. What regulatory areas will interns work on? Interns will work on pharma, medical devices, biologics, CTD/eCTD dossiers, and regulatory intelligence.
How to Apply
Interested candidates can apply using the following methods:
The Regulatory Affairs Intern position at ArtiXio is an excellent opportunity for pharmacy and life sciences students who want to build a strong foundation in global regulatory affairs. With a paid stipend, remote working, live regulatory projects, and PPO potential, this internship can act as a career-launching platform in Regulatory Affairs and compliance consulting.
If you are serious about a long-term career in pharma regulatory affairs, this internship is worth applying for.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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Pharma Duniya is a trusted pharma education and career guidance platform dedicated to B.Pharm, M.Pharm, Pharm.D, MSc, BSc, and Life Sciences students. We publish verified pharma job updates, walk-in interviews, internships, career guides, and interview preparation content to help students and professionals grow in the pharmaceutical and healthcare industry.
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