Regulatory Affairs Intern at ArtiXio in Remote
Company Overview
ArtiXio is an emerging life sciences consulting organization that supports pharmaceutical, medical device, and healthcare companies with regulatory strategy, compliance, and global submissions. Operating with a modern, technology-driven approach, ArtiXio works closely with clients across different regions to help them meet international regulatory requirements efficiently. The company is known for providing practical, project-based exposure to young professionals who want to build strong careers in regulatory affairs and compliance consulting.
With a focus on quality, accuracy, and continuous learning, ArtiXio offers an excellent environment for fresh graduates and students who want to gain real-world experience in global regulatory systems while working remotely. Regulatory Affairs Intern at ArtiXio in Remote
Job Location & Employment Type
- Job Location: Remote (India)
- Base Location: Hyderabad, Telangana
- Employment Type: Paid Internship
- Work Mode: Fully Remote
- Industry: Pharmaceutical & Life Sciences Regulatory Consulting
Open Positions / Department Details
- Position Name: Regulatory Affairs Intern
- Department: Regulatory Affairs & Compliance Consulting
- Number of Positions: Multiple (based on project requirements)
- Suitable For: Freshers, final-year students, and recent graduates
This internship role is designed for candidates who want structured exposure to regulatory affairs across pharmaceuticals, medical devices, biologics, and related healthcare products. Regulatory Affairs Intern at ArtiXio in Remote
Key Roles & Responsibilities
Selected candidates will be actively involved in ongoing regulatory projects under the guidance of experienced regulatory professionals. Responsibilities may include, but are not limited to: Regulatory Affairs Intern at ArtiXio in Remote
- Conducting detailed research on global regulatory guidelines applicable to pharmaceuticals, medical devices, biologics, and nutraceuticals.
- Assisting in the preparation, review, and maintenance of regulatory documentation required for international submissions.
- Supporting lifecycle management activities such as variations, renewals, amendments, and post-approval changes.
- Working with CTD and eCTD dossier structures and understanding module-wise documentation requirements.
- Tracking updates from global health authorities and regulatory agencies to support regulatory intelligence activities.
- Maintaining internal regulatory databases, trackers, and compliance records accurately.
- Preparing summaries, reports, and presentations for internal teams and external clients.
- Collaborating with senior consultants on live client projects and learning regulatory consulting workflows.
- Supporting internal knowledge-building initiatives related to regulatory trends, policies, and compliance standards.
This role offers hands-on learning rather than theoretical exposure, making it highly valuable for candidates aiming to build long-term careers in regulatory affairs. Regulatory Affairs Intern at ArtiXio in Remote
Eligibility Criteria
Education
Candidates should meet one of the following educational requirements:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- MSc in Life Sciences or related disciplines
- Biotechnology or equivalent life sciences qualification
- Regulatory Affairs or regulatory-focused academic background
Final-year students awaiting results may also apply if they can commit to the internship duration.
Experience
- Freshers are encouraged to apply.
- No prior industry experience is mandatory.
- Candidates with academic projects, internships, or certifications related to regulatory affairs will have an added advantage.
Skills Required
- Strong interest in pharmaceutical and healthcare regulatory systems.
- Basic understanding of global regulatory authorities such as USFDA, EMA, CDSCO, and ICH guidelines.
- Good research and analytical skills for reviewing regulations and guidance documents.
- Proficiency in MS Word, Excel, and PowerPoint for documentation and reporting.
- Attention to detail and ability to manage regulatory data accurately.
- Good written and verbal communication skills in English.
- Willingness to learn, adapt, and work in a fast-paced consulting environment.
Regulatory Affairs Intern at ArtiXio in Remote
Salary & Benefits
- Stipend: ₹15,000 – ₹25,000 per month (indicative)
- Compensation Type: Paid Internship
- Other Benefits:
- Practical exposure to global regulatory affairs projects
- One-to-one mentorship from experienced regulatory professionals
- Learning opportunities across pharma, medical devices, and biologics regulations
- Exposure to regulatory consulting and client-facing work
- Strong potential for Pre-Placement Offer (PPO) based on performance
- Remote working flexibility
Selection Process
The selection process for the Regulatory Affairs Intern position may include the following stages:
- Application screening based on educational background and interest in regulatory affairs.
- Initial interaction or interview with the regulatory or HR team.
- Final selection based on suitability, communication skills, and learning mindset.
Only shortlisted candidates will be contacted for further steps. Regulatory Affairs Intern at ArtiXio in Remote
How to Apply
Interested and eligible candidates can apply using the following method:
- Apply via Email: careers@artixio.com
Applicants are advised to send an updated resume highlighting their education, regulatory interest, and any relevant academic or internship experience. Regulatory Affairs Intern at ArtiXio in Remote
Important Dates
- Job Posted On: 22 January 2026
- Application Deadline: Not specified (apply at the earliest)
Why Apply for This Pharma Job?
This Regulatory Affairs Internship at ArtiXio is an excellent opportunity for candidates who want more than classroom learning. The role provides direct exposure to real regulatory projects, helping interns understand how global submissions and compliance work in the pharmaceutical and healthcare industries. Regulatory Affairs Intern at ArtiXio in Remote
Unlike many internships that are limited to observation, this position allows interns to actively contribute to documentation, research, and regulatory intelligence tasks. The remote working model also makes it accessible to candidates across India, while the paid structure ensures professional value for the time invested.
For freshers aiming to build a career in regulatory affairs, consulting, or global pharma compliance, this internship can serve as a strong foundation and may open doors to full-time opportunities through performance-based PPOs. Regulatory Affairs Intern at ArtiXio in Remote
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical job information platform. We are not directly associated with ArtiXio or any hiring organization. Job details are shared for informational purposes only. Candidates are advised to verify all information directly with the employer before applying. Regulatory Affairs Intern at ArtiXio in Remote
Final Call-to-Action
If you are a pharmacy or life sciences graduate looking to begin your professional journey in Regulatory Affairs with real-world exposure, this remote paid internship at ArtiXio could be the right starting point. Review the eligibility criteria carefully and apply as soon as possible to take the next step toward a career in global regulatory affairs. Regulatory Affairs Intern at ArtiXio in Remote
