Software Test Manager Tijuana, MX (Hybrid)
Full-time
Description
<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left">Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have improved the lives of hundreds of thousands of patients by using innovative technology that is wearable, waterproof, and lifestyle accommodating.</p><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left">We are looking for highly motivated, performance driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!</p></div></div></div></div><p style="text-align:inherit"></p><p><b><span style="font-size:14px">osition Overview</span></b></p><p><span style="font-size:14px">This position is responsible for Software Test Manger leading software test activities throughout the Software Development Lifecycle for new product development and sustenance initiatives. This includes ensuring that the software test process and methodologies are compliant with applicable standards, regulations and software test guidance for medical devices. This role will interface with other Insulet departments (e.g. Software Development, System Engineering, Hardware team, Manufacturing, Quality assurance and Regulatory Affairs) as well as other external parties on issues related to product development, launch and product support. The ability to effectively communicate software test design development, applicable regulations, optimize the verification process, and ensure ambiguities and conflicting requirements are resolved are critical to the success of the position. This position also includes direct reports.</span></p><p> </p><p><b><span style="font-size:14px">Responsibilities</span></b></p><ul><li><p><span style="font-size:14px">Manage the software testing team and ensure Software verification is conducted in accordance with the FDA standards to deliver high quality software.</span></p></li><li><p><span style="font-size:14px">Manage a team of 4-8 software application Manual/SDET test engineers.</span></p></li><li><p><span style="font-size:14px">Mange Design Control and Software Test initiatives to develop appropriate Design History File documents for FDA Class II and Class III medical devices.</span></p></li><li><p><span style="font-size:14px">Responsible for the generation, review and approval of design control documentation with primary focus on software test deliverables.</span></p></li><li><p><span style="font-size:14px">Collaborate with Project Management to support and optimize the schedules.</span></p></li><li><p><span style="font-size:14px">Support software development teams on the validation of software tools.</span></p></li><li><p><span style="font-size:14px">Work with software, hardware, user experience, marketing, manufacturing, and quality assurance on generation, documentation, verification and validation of requirements.</span></p></li><li><p><span style="font-size:14px">Lead the creation of necessary documentation to comply with regulatory requirements and industry best practices.</span></p></li><li><p><span style="font-size:14px">Establish and maintain software test programs, processes, procedures and controls to ensure compliance with FDA regulations and established standards such as IEC 62304.</span></p></li><li><p><span style="font-size:14px">Ensures compliance to IEC 62304, and FDA Guidance on Software Contained in a 510(k) Submission.</span></p></li><li><p><span style="font-size:14px"> Provide guidance and participate in software development activities including design and code reviews, requirements analysis and tracing, defect tracking and configuration management, review requirements, specifications, product design documents, validation protocols, test plans, test cases, and other documentation as required and provide timely feedback.</span></p></li><li><p><span style="font-size:14px">Applies a good working knowledge of Software Development Life Cycle (IEC 62304), Design Controls (ISO 13485) and other regulatory requirements and agencies as it relates to software test activities in software development.</span></p></li><li><p><span style="font-size:14px">Work closely with the software development team to identify improvements.</span></p></li><li><p><span style="font-size:14px">Influence the requirements definition and software design to maximize testability.</span></p></li><li><p><span style="font-size:14px">Oversee and influence development of test objects to meet needs of protocol.</span></p></li><li><p><span style="font-size:14px">Develop and extend protocols and plans as device features evolve.</span></p></li><li><p><span style="font-size:14px">Participate in product design reviews.</span></p></li><li><p><span style="font-size:14px">Represent software test in the core team meetings.</span></p></li><li><p><span style="font-size:14px">Creating and executing test plans, test designs and test cases and generating test reports.</span></p></li><li><p><span style="font-size:14px">Creating and updating Trace matrices between requirements and Tests.</span></p></li><li><p><span style="font-size:14px">Work with the scrum Master and product owners to prioritize or deprioritize the backlog.</span></p></li><li><p><span style="font-size:14px">Keep track of the Testing board and tools inventory for the team.</span></p></li><li><p><span style="font-size:14px">Performs other duties as required.</span></p></li></ul><p> </p><p><b><span style="font-size:14px">Required Leadership/Interpersonal Skills & Behaviors</span></b></p><ul><li><p><span style="font-size:14px">Self-motivated</span></p></li><li><p><span style="font-size:14px">Proactive</span></p></li><li><p><span style="font-size:14px">Quick learner</span></p></li><li><p><span style="font-size:14px">Mentor</span></p></li><li><p><span style="font-size:14px">Ability to represent the team cross functionally.</span></p></li><li><p><span style="font-size:14px">Generate metrics for the team as required.</span></p></li></ul><p> </p><p><b><span style="font-size:14px">Required Skills and Competencies</span></b></p><ul><li><p><span style="font-size:14px">Effective verbal and written communication skills.</span></p></li><li><p><span style="font-size:14px">Working knowledge of software testing tools.</span></p></li><li><p><span style="font-size:14px">Able to communicate at multiple levels of an organization.</span></p></li><li><p><span style="font-size:14px">Deep knowledge of software testing (Manual, Automation and code Inspection)</span></p></li><li><p><span style="font-size:14px">Software test group experience strongly preferred.</span></p></li><li><p><span style="font-size:14px">Strong written, verbal, interpersonal and presentation skills</span></p></li></ul><p> </p><p><b><span style="font-size:14px">Education and Experience</span></b></p><ul><li><p><span style="font-size:14px">BS in Software Engineering, Computer Science or similar field; 6-8 years hands on experience in software testing in regulated industry and/or equivalent combination of education and experience.</span></p></li><li><p><span style="font-size:14px">Experience of 1+ years being the Software Test Lead/Manager.</span></p></li><li><p><span style="font-size:14px">Thorough understanding of software test principles, practices and metrics as well as software development and testing best practices that foster high quality software.</span></p></li><li><p><span style="font-size:14px">Hands on experience using modern software development and software test tools.</span></p></li><li><p><span style="font-size:14px">Proven record developing and executing software test protocols for complex medical devices.</span></p></li><li><p><span style="font-size:14px">Familiarity with IEC 62304, ISO 14971, FDA regulations and international standards applicable to medical device software development, verification and validation a plus.</span></p></li><li><p><span style="font-size:14px">Experience working with products from the prototype through 510(k)/ISO clearance and commercialization is preferred.</span></p></li></ul><p> </p><p><b><span style="font-size:14px">Additional Information</span></b></p><p><span style="font-size:14px">NOTE: This position is eligible for hybrid working arrangements (requires on-site work from an Insulet office at least 1x/week; may work remotely other days). #LI-Hybrid </span></p><p><span style="font-size:14px"> </span></p>
Insulet
BIOTECHNOLOGY
Insulin Pump
LocationACTON, MA
Employees201-500
Open Jobs390
Metabolic Diseases
View Company ProfilePipeline
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