Manishmedi Innovations
Website:
manishmediinnovation.net
Job details:
Company Description ManishmediInnovation is dedicated to providing high-quality medical products to healthcare providers worldwide, with a strong focus on urology, gastroenterology, infertility/gynecology, and radiology. The company collaborates closely with leading medical doctors and has built 15 years of experience in developing products that meet demanding clinical requirements. ManishmediInnovation’s solutions are used successfully in more than 40 countries, reflecting its global reach and commitment to quality. The organization adheres to internationally recognized standards and holds certifications including ISO 9001:2003, ISO 13485, EC, and Biocompatibility. This combination of clinical collaboration, global presence, and rigorous certification makes it a stable and quality-driven environment for professionals in the medical sector.
Role Description This is a full-time, on-site role based in Bengaluru. The role involves supporting the development, coordination, and promotion of medical products within the company’s key specialties, ensuring that product information and documentation are accurate and aligned with clinical requirements. Day-to-day tasks may include collaborating with internal teams and healthcare professionals, maintaining product records, assisting in quality-related activities, and contributing to process improvements. The role also requires participating in meetings, preparing reports, and supporting cross-functional projects that help enhance product performance and customer satisfaction. The position calls for a detail-oriented and proactive professional who is comfortable working in a regulated medical environment and engaging with technical and clinical information.
Qualifications
- Background in healthcare, biomedical engineering, life sciences, or a related medical field, with an understanding of urology, gastroenterology, infertility/gynecology, or radiology considered an advantage.
- Experience working with medical products or devices, including familiarity with quality standards, regulatory requirements, or certification processes such as ISO 9001 and ISO 13485.
- Strong analytical and documentation skills, including the ability to interpret clinical or technical information and prepare clear, accurate reports and records.
- Effective communication and collaboration skills for working with cross-functional teams and medical professionals in a structured, regulated environment.
- Proficiency with basic office software and tools, strong organizational skills, and a high level of attention to detail.
- Ability to work on-site in Bengaluru on a full-time basis, demonstrating reliability, adaptability, and a commitment to continuous learning.
- Previous experience in a medical manufacturing, medical products, or healthcare solutions company is beneficial.
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