Infinity MedTech Consultants is hiring for the position of QA / RA Intern to join its team in Ahmedabad, Gujarat. This paid internship opportunity is ideal for freshers and candidates with 0–1 year of experience looking to build a career in medical device quality assurance and regulatory affairs.
The internship program offers hands-on exposure to medical device regulatory affairs, ISO 13485 standards, quality management systems (QMS), technical documentation, and USFDA regulatory processes.
About Infinity MedTech Consultants
Headquartered in Lucknow, Infinity MedTech Consultants operates as a specialized medical device consulting firm for India, supporting clients with USFDA, ISO, technical documentation, 3D design, training, and certifications.
The organization’s core specialties include medical device consultancy, 510(k) submissions, CDSCO registrations, ISO 13485 compliance, CAD design, technical documentation, and country registrations. The firm works closely with medical technology developers and manufacturers to ensure compliance with domestic and international regulatory frameworks.
For more information, visit the official website: https://infinitymedtechconsultants.com/
QA / RA Intern Vacancy Details
Infinity MedTech Consultants is looking for dedicated interns to support its growing medical device consulting operations in Ahmedabad.
- Position: QA / RA Intern
- Industry: Medical Devices
- Location: Ahmedabad, Gujarat
- Experience: Freshers / 0–1 Year
- Employment Type: Paid Internship
Eligibility Criteria and Qualifications
Candidates interested in this internship opportunity should meet the following educational requirements:
Preferred Qualification: B.Tech, M.Tech, B.Pharm, M.Pharm, Biomedical, Biotechnology, or a related field.
Experience Level: Freshers or candidates with 0–1 year of relevant academic or early professional exposure.
Key Responsibilities of the QA / RA Intern
The internship combines learning opportunities with practical responsibilities across quality assurance and regulatory affairs, including:
- Supporting Quality Assurance and Regulatory Affairs activities.
- Assisting in the preparation and review of technical documentation.
- Supporting QMS documentation and Standard Operating Procedure (SOP) activities.
- Assisting with ISO 13485 compliance-related activities.
- Supporting regulatory submissions and documentation.
- Maintaining records, trackers, and document control systems.
- Coordinating with QA and RA teams for ongoing projects.
What You Will Learn During the Internship
Interns will gain practical experience and professional exposure in key areas of medical device compliance, including:
- Medical Device Regulatory Affairs
- ISO 13485 & Quality Management Systems (QMS)
- Technical Documentation
- CDSCO and USFDA regulatory processes
- QA documentation and compliance
How to Apply for This Internship Vacancy
Interested candidates can apply by sharing their updated CV through email provided below:
Application Email: infinitymedtechconsultants@gmail.com
Ensure that your resume highlights your educational background in pharmacy, engineering, biotechnology, or biomedical sciences before applying.
Candidates are advised to verify recruitment communications through official channels before sharing personal or professional documents. Avoid engaging with unverified intermediaries requesting fees or unauthorized payments.
Frequently Asked Questions
1. What qualifications are required for the QA / RA Intern vacancy?
Candidates with a B.Tech, M.Tech, B.Pharm, M.Pharm, Biomedical, Biotechnology, or related degree are eligible to apply.
2. Is prior experience mandatory for this position?
No, the role is open to freshers and candidates with 0–1 year of experience.
3. Where is the internship located?
The position is located in Ahmedabad, Gujarat.
4. How can candidates apply?
Candidates can share their CV via email at infinitymedtechconsultants@gmail.com.