IIT Bombay MSc Biotechnology Project Research Job With High Pay – Apply Online
IIT Bombay MSc Biotechnology Project Research Job With High Pay – Apply Online. Biotechnology jobs. MSc Biotechnology Project Research Associate job. Interested and eligible applicants can check out all of the details on the same below
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INDIAN INSTITUTE OF TECHNOLOGY BOMBAY
POWAI, MUMBAI 400076.
Advertisement No.: IRCC/EXT287/2023
Job Title: Project Research Associate
Job Reference Number: 50493152
Application End Date: 05.09.2023
Type of Employment: Proj. Staff Contract
No. of Position(s): 1
IITB Project Recruitment:
Project title: ICMR-DHR-CoE IIT Bombay
About the project: BETIC, IIT Bombay is a leading center of medical device innovation, with team members drawn from mechanical, Biomed, design, electronics, materials, and software backgrounds, who are working closely with leading doctors to develop, test and commercialize a variety of innovative and affordable products. The center is funded by several government agencies (RGSTC, DST, DBT, BIRAC, ICMR, NSE Foundation and others). ICMR-DHR CoE – BETIC Hub is for medical-grade pilot manufacturing and pre-compliance testing along with relevant expertise and quality management system. The work environment provides considerable scope for learning and networking.
General information:
- The position is temporary for a period of 1 year and tenable only for the duration of the project.
- The appointment is for time bound project and the candidate is required to work mainly for the successful completion of the project. The selection committee may offer lower or higher designation and lower or higher salary depending upon the experience and performance of the candidate in the interview.
- Candidates called for an interview will be required to attend at his/ her own expense.
- For any queries/clarification please contact [email protected].
Essential Qualifications & Experience: MSc in Biotechnology with 2 years of relevant experience
Job Profile:
- Leading the project and relevant design and development of the Medical Devices individually.
- Product officer delivers specific operations to meet the requirements for medical device
development. Define measurable design requirements, regulatory requirements for the project. - Lead in the planning, design, development, prototyping, testing and clinical validation of medical devices.
- Collaborate to build 3D CAD models from engineering drawings or sketches for medical device assemblies, subassemblies, fixtures and tooling.
- Collaborate with engineering teams, coordinate with product teams for development, and report test findings
- Prepare engineering drawings with tolerances and manufacturing plans.
- Interface between various stakeholders to ensure product safety and performance and inform the stakeholders updated on the progress of the product development
- Implement design and development activities as per QMS like ISO 13485.
- Disseminate knowledge and good practices through courses, events, demos, visits, and exhibitions.
- Support training, admin-related, events, and other activities associated with the project.
Pay Details: Level PR-O1: Salary range from Rs.33600 to Rs 67200 + Rs.6250.00/- Out Of Campus Allowance (if applicable) p.m.
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Here are five possible interview questions for the position of Project Research Associate, along with their answers:
Question 1: Can you provide an overview of your educational background and the relevant experience you have in the field of biotechnology, specifically related to medical device development? Answer: Certainly. I hold an MSc degree in Biotechnology and have accumulated 2 years of practical experience in the field. During this time, I have been actively involved in projects related to the design, development, and prototyping of medical devices, which has equipped me with a solid foundation for the role of Project Research Associate.
Question 2: The role involves leading the project and contributing to the design and development of medical devices. Can you share a specific example of a medical device project you have worked on and your role in its design and development? Answer: Of course. In a previous project, I was responsible for leading the design and development of a wearable medical monitoring device. My role included defining design and regulatory requirements, collaborating with engineering teams to create 3D CAD models, conducting prototyping, and overseeing clinical validation. This experience has provided me with insights into the end-to-end process of medical device development.
Question 3: The job profile mentions collaborating with various stakeholders and implementing design and development activities as per ISO 13485. Can you describe how you ensure effective communication and collaboration among different teams and how you adhere to quality management standards? Answer: Effective communication and collaboration are vital in multidisciplinary projects. I ensure regular meetings with engineering and product teams to align objectives, share progress, and address concerns. As for ISO 13485, I have a strong understanding of its requirements and apply them throughout the design and development process, ensuring that the product adheres to quality and regulatory standards.
Question 4: How do you approach the planning and execution of clinical validation for medical devices? Could you elaborate on your role in ensuring the safety and performance of these devices during validation? Answer: Clinical validation is a critical phase. I meticulously plan clinical trials, defining protocols and objectives. My role involves coordinating with medical professionals, collecting and analyzing data, and ensuring that the device meets safety and performance benchmarks. Regular reporting to stakeholders and adjustments based on feedback are crucial to refining the device for its intended use.
Question 5: The role also involves disseminating knowledge and good practices through various means. Can you share an example of an event, course, or exhibition where you’ve showcased your work and engaged with others in the field? Answer: Certainly. I participated in a medical technology exhibition where I presented a prototype of a novel surgical instrument I had contributed to designing. The exhibition provided a platform to interact with industry experts, gather feedback, and share insights. I believe such events are essential for cross-sharing knowledge and learning from peers in the field.
Remember to tailor your responses based on your own experiences and understanding of the role’s requirements.
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Msc biotechnology