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Research Assistant Intern

2 weeks ago

Singapore VENTAS BIO PTE. LTD. Full time

Are you ready to be a part of something transformative? Ventas Bio is not just another medical technology company; we are the change-makers in regenerative medicine With a team of leading scientists and seasoned industry professionals, we take biology to the next level to heal bodies better and faster.

Our "Think Biology" mantra is our DNA. We are obsessed with pioneering new paths in tissue and bone regeneration and wound healing, and we are just getting started

So, if you are as passionate about pushing the boundaries of medicine as we are, hop on board Let's shape the future, redefine healing, and improve lives together.

**Position Overview**:
As a Research Assistant Intern focusing on regulatory affairs, you will support our research and compliance teams in ensuring that our medical devices and biologics meet all regulatory requirements. Your role will involve conducting literature reviews, data collection and analysis, report preparation, and assisting with regulatory submissions. We are looking for a detail-oriented, enthusiastic individual eager to learn and contribute to our mission of advancing healthcare.

**Key Responsibilities**:

- Conduct comprehensive literature reviews and synthesize relevant findings to support regulatory submissions.
- Assist in the design and implementation of research methodologies and experiments related to regulatory compliance.
- Collect, analyze, and interpret data from preclinical and clinical studies.
- Prepare detailed research reports, regulatory documents, presentations, and manuscripts for publication.
- Support the preparation and submission of regulatory filings, including Investigational Device Exemptions (IDEs), 510(k) notifications, and Biologics License Applications (BLAs).
- Coordinate and manage research-related administrative tasks, including maintaining regulatory documentation and databases.
- Collaborate with team members to ensure compliance with local and international regulatory standards (e.g., FDA, EMA, HSA).
- Participate in team meetings and contribute to discussions on research findings, regulatory strategies, and compliance issues.

**Qualifications**:

- Currently pursuing or recently completed a degree in Regulatory Affairs, Biomedical Engineering, Life Sciences, or a related field.
- Strong understanding of regulatory requirements and guidelines for medical devices and biologics.
- Excellent analytical and critical thinking skills.
- Superior written and verbal communication abilities.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Experience with statistical software (e.g., SPSS, R, Stata) is a plus.
- Ability to work both independently and collaboratively.
- High attention to detail and strong organisational skills.
- Passionate about regulatory affairs and eager to develop new skills in the medical device and biologics sectors.

**What We Offer**:

- Hands-on experience in a dynamic and collaborative research and regulatory environment.
- Mentorship and guidance from experienced professionals in regulatory affairs.
- Opportunities to contribute to impactful and meaningful projects in healthcare.
- A supportive and inclusive work culture.
- Potential for future career opportunities within the organization.