Serigen Mediproducts Pvt. Ltd., an innovation-driven tissue regeneration products company, is offering a 6-month Regulatory Affairs Internship in Pune, Maharashtra. This opportunity is perfect for life sciences, pharmacy, biomedical engineering, and regulatory affairs students or freshers who want hands-on experience in the medical device industry.
This internship provides exposure to regulatory compliance, clinical trial documentation, and product registration processes essential for bringing medical devices to the Indian market.
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Key Responsibilities
As a Regulatory Affairs Intern, you will:
- Assist in compiling and reviewing clinical trial documentation such as study protocols, informed consent forms, and clinical evaluation reports.
- Maintain regulatory databases and tracking systems for product registrations and submissions.
- Conduct research on regulatory requirements for medical devices and clinical trials.
- Assist in preparing documents for regulatory approvals in India.
- Support senior management and perform additional tasks as assigned.
Qualifications
Ideal candidates should have:
- Current enrollment or a recent degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, or related fields.
- Strong attention to detail and organizational skills.
- Excellent written and verbal communication skills in English.
- Ability to work collaboratively in a team environment.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Benefits
- Practical experience in Regulatory Affairs within the medical device industry.
- Exposure to real-world regulatory compliance and clinical trial processes.
- Networking opportunities with industry professionals.
- Mentorship and learning opportunities within a dynamic team.
How to Apply
Interested candidates can apply by filling out the Google Form below:
Apply Here
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