Regulatory Affairs Intern

Roles & Responsibilities

• Research global regulatory requirements for pharmaceuticals, medical devices, biologics, and nutraceuticals
• Support preparation, review, and lifecycle management of CTD and eCTD dossiers
• Assist with regulatory submissions, variations, renewals, and post-approval changes
• Track global regulatory updates, approvals, guidelines, and policy changes
• Maintain and update regulatory databases and regulatory intelligence tools
• Support development of client presentations, regulatory reports, and internal knowledge content
• Collaborate with senior regulatory consultants on active client projects
• Assist in documentation review, data analysis, and compliance-related activities

Qualification

• Pursuing or recently completed B.Pharm, M.Pharm, MSc (Life Sciences), Biotechnology, or Regulatory Affairs

Experience

• Freshers or students with academic exposure to Regulatory Affairs are encouraged to apply
• Prior internship, project work, or coursework in regulatory affairs is an advantage

Skills

• Strong interest in global regulatory frameworks including USFDA, EMA, CDSCO, and ICH
• Good understanding of regulatory documentation and submission processes
• Proficiency in MS Word, Excel, and PowerPoint
• Strong research, analytical, and documentation skills
• Detail-oriented with good written and verbal communication
• Ability to work independently and adapt in a startup consulting environment

About the Organisation

ArtiXio is a fast-growing life sciences consulting startup delivering regulatory affairs, compliance, and regulatory intelligence solutions to global pharmaceutical, medical device, and biotech companies. With a strong focus on practical learning and real-world exposure, ArtiXio provides interns and professionals the opportunity to work on live regulatory projects while building industry-relevant skills in a dynamic consulting environment.