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Live In Fda Scientist Jobs in Indiana (NOW HIRING)

Elanco

Sr Research Scientist

Indianapolis, IN · Hybrid

$94K - $120K/yr

As a global leader in animal health, we are dedicated to innovation and delivering products and ... g., FDA/CVM, EMA) on analytical topics. What will give you a competitive edge (preferred ...

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Live In Fda Scientist information

What is the difference between Live In Fda Scientist vs Fda Reviewer?

AspectLive In Fda ScientistFda Reviewer
Required credentialsBachelor's or Master's in Life Sciences, relevant experienceSimilar credentials, often with advanced degrees
Work environmentOn-site, often in government or research facilitiesOffice-based, reviewing submissions at FDA headquarters or regional offices
Employer and industry usageFederal government, regulatory scienceFederal government, regulatory review
Common search intentJob duties, qualifications, work conditionsComparison of roles, responsibilities, career path

The Live In Fda Scientist and Fda Reviewer roles both require scientific expertise and federal employment credentials. While the Live In Fda Scientist often involves conducting research and scientific analysis on-site, the Fda Reviewer primarily focuses on evaluating regulatory submissions and documentation. Both roles are integral to FDA operations, but they differ in daily tasks and work environment, with the scientist more research-oriented and the reviewer more review-focused.

Is it hard to get hired by the FDA?

Getting hired as a Live In FDA Scientist can be competitive due to strict qualification requirements, including relevant education, experience, and certifications such as a background in regulatory science or laboratory work. The hiring process often involves multiple interviews, background checks, and demonstrating expertise in areas like compliance, data analysis, and scientific research.

What are the key skills and qualifications needed to thrive as a Live-In FDA Scientist, and why are they important?

To thrive as an FDA Scientist, you need a strong background in life sciences or chemistry, typically with an advanced degree (MS or PhD) and experience in research or regulatory affairs. Familiarity with laboratory instrumentation, data analysis software, and FDA regulatory systems is essential, and certifications like RAC (Regulatory Affairs Certification) can be advantageous. Attention to detail, critical thinking, and excellent communication skills help you interpret data accurately and collaborate effectively with multidisciplinary teams. These skills ensure scientific integrity, regulatory compliance, and the advancement of public health through safe and effective products.

What is a Live In FDA Scientist?

A Live In FDA Scientist typically refers to a regulatory scientist who works for the U.S. Food and Drug Administration (FDA) and may be involved in on-site or continuous monitoring of studies, often in clinical or laboratory settings. Their role includes evaluating scientific data, ensuring compliance with federal regulations, and overseeing the safety and efficacy of products such as drugs, biologics, or medical devices. Live-in positions might be required for research facilities needing 24/7 oversight, although such roles are rare and specialized. These scientists play a crucial role in public health by supporting the FDA’s mission to protect consumers.

What are some unique challenges faced by a Live-In FDA Scientist, and how can they be managed?

A Live-In FDA Scientist often works in environments such as research facilities or clinical trial sites where on-site presence is essential. This setup can present challenges like maintaining work-life balance, adapting to extended hours, and managing confidentiality due to the sensitive nature of ongoing research. Successful candidates typically develop strong time management skills, set clear personal boundaries, and foster open communication with team members to ensure both professional responsibilities and personal well-being are balanced. Collaboration with multidisciplinary teams is frequent, and adaptability is key to thriving in this dynamic role.
What are the most commonly searched types of Fda Scientist jobs in Indiana? The most popular types of Fda Scientist jobs in Indiana are:
What cities in Indiana are hiring for Live In Fda Scientist jobs? Cities in Indiana with the most Live In Fda Scientist job openings:
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Senior Software Engineer for Medical Device Startup

Senior Software Engineer for Medical Device Startup

Levisonics

Fishers, IN • On-site, Remote

$114K - $151K/yr

Other

Medical, Dental, Vision, PTO

Posted 18 days ago

Job description

About Us: 
We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device. Our full-time team currently comprises a CEO/Biomedical Engineer, and an Electrical Engineer. 

Job Summary: 
We are seeking a talented and experienced Senior Software Engineer to join our team and lead the development and optimization of software workflows for our innovative acoustic tweezing technology-based medical devices. The ideal candidate will have a Master's degree in Computer Science, Software Engineering, or a related field, with a minimum of 5 years of experience. This role requires strong coding skills in Python and C/C++, proficiency in developing intuitive and visually engaging graphical user interfaces, and expertise in SQL for effective data management and database design. Experience with version control systems, particularly Git, is essential, along with the ability to understand and generate code from workflow diagrams. As the first and only software engineer on the team, you will play a pivotal role in shaping the software development efforts for our groundbreaking technology. This role is critical to the success of our product and involves working on multiple federal grants and projects. 

Startup Environment: 
We operate in a fast-paced startup environment where innovation, adaptability, and a proactive mindset are key to success. We are looking for individuals who are passionate about working in a startup setting and thrive in dynamic and challenging situations. We value individuals who are not just seeking a job but are driven by a genuine passion for creating impactful solutions and driving change in the medical device industry. Our team members are expected to work well under pressure, juggle multiple projects, and be flexible in their roles as the needs of the company evolve. If you are excited about the opportunity to make a meaningful impact and are ready to roll up your sleeves and tackle challenges head-on, we encourage you to apply. 

Key Responsibilities: 

  1. Optimize and Enhance Existing Software: 

  • Improve the efficiency of our existing software written in Python. 

  • Increase processing speed for short-term operation on laptops. 

  • Convert and optimize the software for embedded computing devices inside the medical device long-term. 

  1. Software Packaging and Security: 

  • Secure the code to prevent reverse engineering. 

  • Package the software into executable files for easy installation and deployment. 

  1. Connectivity and Data Management: 

  • Ensure the software can connect to the internet. 

  • Implement connectivity to an online database for long-term data management. 

  • Incorporate Data Science, Machine Learning, and AI for handling large amounts of health data. 

  1. Health Data Security: 

  • Ensure the highest level of security for software and health data management. 

  1. New Technique Development: 

  • Convert and develop existing crude MATLAB codes and technology algorithms into efficient software for commercial use. 

  • Create executable files with efficient large data handling capabilities. 

  • Develop complex data processing software and manage large data analysis. 

  • Develop a user-friendly interface for healthcare professionals. 

  • Implement a remote kill switch for the software. 

  • Apply all relevant requirements from existing software. 

  1. Parallel Processing and Language Conversion: 

  • Implement efficient parallel processing techniques. 

  • Convert existing Python code to C/C++ or another suitable low-level efficient language to run software optimally on embedded hardware. 

  1. Other Responsibilities: 

  • Develop high-quality, efficient, and maintainable code. 

  • Design intuitive and visually engaging user interfaces. 

  • Proactively take on new responsibilities and suggest innovative ideas for product and company growth. 

  • Participate in grant writing and fundraising activities. 

  • Engage in FDA-related activities and adhere to quality protocols. 

  • Perform other relevant software-related tasks as needed for the company. 

Minimum Qualifications: 

  • Master’s degree in Computer Science, Software Engineering, or a related field. 

  • Minimum of 5 years of experience in software development. 

  • Strong coding skills in Python, C, and C++ (JavaScript is a plus). 

  • Proficiency in developing intuitive and visually engaging graphical user interfaces. 

  • Proficiency in SQL for effective data management and database design. 

  • Experience with version control systems, particularly Git. 

  • Ability to understand and generate code from workflow diagrams. 

  • Knowledge of integrating multiple devices and establishing centralized control. 

  • Familiarity with IDEs, preferably PyCharm. 

  • Excellent problem-solving skills and ability to work independently. 

  • Strong written and verbal communication skills. 

Preferred Qualifications: 

  • Experience working in the medical device industry. 

  • Familiarity with Agile development methodologies. 

  • Knowledge of machine learning techniques and algorithms. 

  • Experience with Docker and containerization technologies. 

  • Familiarity with cloud platforms such as AWS or Azure. 

  • Prior experience working in startups. 

  • Experience with embedded systems and medical device software development. 

  • Strong knowledge of data security, especially related to health data. 

  • Knowledge of parallel processing and algorithm optimization. 

  • Innovative mindset with a track record of proactive contributions. 

  • Experience in grant writing and regulatory compliance (FDA). 

What We Offer: 

  • Competitive salary 

  • Health, dental, and vision insurance coverage 

  • Generous paid time off 

  • Professional development opportunities 

  • Potential to receive stock options 

  • Opportunities for growth within the company 

  • Flexible work arrangements, including remote work options 

  • Dynamic and innovative startup environment 

  • Opportunity to make a meaningful impact in the medical device industry

Apply