Kentro Spine @ Rivarp Medical Pvt. Ltd.
Website:
rivarpmedical.com
Job details:
Company Description Rivarp Medical Pvt. Ltd. is a medical device company founded by professionals with decades of experience in design and development, manufacturing, marketing, sales, and distribution. The team has worked extensively in India and major global markets, bringing deep industry knowledge and regulatory familiarity. Rivarp Medical focuses on delivering high-quality, reliable medical devices that support better clinical outcomes and patient safety. The company fosters a collaborative, innovation-driven culture where diverse expertise is valued and knowledge sharing is encouraged. Team members have the opportunity to contribute to products that directly impact healthcare delivery worldwide.
Role Description This is a full-time, remote role focused on surgical implant devices at Rivarp Medical. The professional in this role will support the lifecycle of surgical implant products, including reviewing design documentation, assisting with product specifications, and collaborating with cross-functional teams such as engineering, quality, and regulatory. Daily tasks may include preparing and updating technical files, supporting clinical and market research activities, and assisting in the development of training and educational materials for healthcare professionals. The role will also involve coordinating with manufacturing and supply chain teams to ensure product quality, availability, and compliance with relevant standards. In addition, the individual will help create product-related content for internal and external stakeholders, respond to technical inquiries, and contribute to continuous improvement initiatives for the surgical implant portfolio.
Qualifications
- Strong foundation in medical devices or biomedical engineering, with familiarity in surgical implant concepts, materials, and basic anatomy/physiology.
- Experience or coursework related to product lifecycle activities such as design support, documentation, quality, or regulatory compliance in the medical device or healthcare sector.
- Excellent written and verbal communication skills, with the ability to prepare clear technical documentation, reports, and training materials for diverse audiences.
- Demonstrated ability to work independently in a remote setting, manage multiple tasks, and collaborate effectively with cross-functional and cross-cultural teams.
- Proficiency with standard productivity tools (e.g., spreadsheets, presentations, document management systems) and comfort working with digital collaboration platforms.
- Bachelor’s degree in biomedical engineering, mechanical engineering, life sciences, healthcare, or a related field; advanced degrees or relevant certifications are a plus.
- Understanding of medical device quality systems and regulatory frameworks (e.g., ISO standards, regional regulations) is highly desirable.
- Prior experience in surgical implants, operating room environments, or clinical support roles is an advantage but not mandatory.
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