The ISM is a key leadership role responsible for the development, implementation, and management of the organization's information security program. The ISM will lead efforts to protect the organization's information assets and infrastructure from cybersecurity threats, ensuring the confidentiality, integrity, and availability of information systems and in medical devices across multiple projects.

　　This is an on-site role in Manchester New Hampshire’s burgeoning technology center. Remote will not be considered. 

　　How you will make an impact:

　　Ensuring compliance with FDA and HHS guidance for the management of cybersecurity in medical devices across multiple projects.

　　Ensuring compliance with Quality System Regulations, ISO 13485, TODO and company Quality System and project specific procedures

　　Providing expertise in security policies and best practices as detailed in in cybersecurity as recommended by leading security frameworks and standards (ie: NIST, CMMP, ISO 27001, SANS Institute, CWE, OWASP, coding standards, and static analysis rule sets)

　　Identifying vulnerabilities in our current network.

　　Keeping up to date with developments in Information security standards and threats.

　　Performing or coordinating penetration tests.

　　Collaborating with IT and project managers to improve security.

　　Documenting any security incidents or breaches and assessing their damage.

　　Educating colleagues about best practices for information security.

　　Representing Company and Affiliates for FDA audits or client audits

　　Skills you will need to be successful:

　　Computer Science, Information Technology, or Engineering degree

　　10+ years of experience designing and implementing large, secure and scalable systems

　　3-5 years experience with NIST and ISO requirements

　　Demonstrated ability to deliver safety critical systems that meet or exceed federal and industry standards for cybersecurity

　　Demonstrated ability to lead technical product teams, using a risk-based SDLC approach

　　Experience with medical devices or FDA regulated software development

　　Experience with cloud-based services

　　Excellent communication skills

　　Strong problem solving skills

　　Strong documentations skills and a good cultural fit will be important

　　Must be able to work on-site at DEKA

　　Desired skills and experience:

　　Experience in an Agile environment

　　Experience in developer operations/cloud operations

　　Solid understanding of Object Oriented design, programming principles, and REST interfaces

　　About DEKA:

　　One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.

　　Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

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