• Build and support software that uses AI and machine learning to solve real business problems • Develop code using Python, Java, or C++ • Use machine learning libraries such as TensorFlow, PyTorch, or scikit-learn • Analyze data using SQL and apply math concepts like linear algebra, probability, and statistics • Work with engineers, product managers, and analysts to design solutions • Help troubleshoot and improve complex systems • Share your findings and explain technical concepts to teammates • Stay current with new tools, trends, and technologies in AI, ML, and cloud engineering

• As an Entry-Level Product Engineer, you will help build digital products that make a real impact • You will work with modern technologies, learn strong engineering practices, and collaborate with other engineers, product managers, and designers. • Use programming languages and modern tech stacks to build and enhance applications • Apply core concepts like algorithms, data structures, database normalization, and coding best practices • Learn and use modern engineering techniques such as TDD (Test Driven Development), CI/CD (Continuous Integration/Continuous Delivery) • Identify processes that can be automated and build solutions that make teams more efficient • Support the full product lifecycle from coding to deployment • Write software that supports real value for the product and the business • Help write technical stories, estimate effort, and partner with a Digital Product Manager on prioritization • Use human-centered design principles to ensure solutions work well for the people using them.

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Whether you’re an experienced professional or just getting started, your contributions matter at Fortra. If you’re passionate about tackling meaningful challenges alongside talented team members committed to helping each other succeed, all while having lots of fun, we want to hear from you. Outflank security tooling is a Fortra product that offers attack simulation software to its end-users. The product is offered as a cloud portal but also contains various stand-alone/local web components. Via the cloud portal, customers can configure the tools, and once configured, OST then creates the specific malware artifact/hacking tool by compiling specific code (C, C++, assembly) on demand. The full stack developer works on creating a stable front and backend for exposing highly technical configurations. Mainly working in Python, but some experience with C/C++ or compilers is preferred. What You'll Do - Together with the security researchers, finalize offensive tools and implement them in the OST portal or other Fortra security platforms. - Contribute ideas and efforts towards internal projects and work as part of a team to determine the best approach for various initiatives. - Work closely with the Outflank team to prioritize and troubleshoot reported issues. - Work collaboratively with other internal developers in a multi-dev environment (Git). - Maintain, manage, and improve the OST portal (speed, security, additional tools). Qualifications - Bachelor’s degree in computer science/web development or related. - 5+ years of professional full stack development experience. - Proficient in Python; preferably Python/C/C++. - Experience with automated testing and test frameworks. - Can and will write clear documentation along with the code. - Preferably some experience with reverse engineering, assembly or other security-related tinkering with low-level code. - Preferably experience with Scrum, Jira, CI/CD, Git. - Preferably interest in, or experience with Security/ethical hacking for better understanding of our products and core values. - You take ownership and have a quite informal way of working (Scrum/Kanban oriented). - You are proactive, communicative, and solution-oriented. - Have a high level of proficiency in business English. - Have the highest ethical standards that are required for the sensitive work we do. Some of our work requires screening by authorities. Working Hours & Location - Residing in either the EU or US. Collaborating with teams in Central European and US east coast. - Periodic meetups 'bootcamps’ to collaborate, thus preferably residing with easy travel options to Amsterdam, NL. Benefits - Competitive benefits and salaries. - Personal and professional development opportunities. - Flexibility. - Much more!

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Reporting to Director, Supplier Quality the Senior Engineer, Supplier Quality will support key operational pillars of the Supplier Quality Program: - Supplier Change Notification Program - Supplier Qualification - Quality Technical Agreements - Supplier GxP Certificate Management - Scorecard Assessments & Performance Monitoring The scope of this role includes commercial and development (clinical) GMP. You will be responsible for assisting in day-to-day management of the Supplier Quality Processes. You will partner with cross-functional stakeholders and external suppliers to support qualification and monitoring activities, drive regulatory compliance, reduce risk, and implement continuous improvements that strengthen supplier performance across the product lifecycle. What You'll Do - Partner with cross-functional SMEs and Business owners in selection, qualification, and onboarding of new suppliers. - Lead the Supplier Change Notification program by reviewing, assessing, and coordinating Supplier Change Notifications with internal stakeholders and external suppliers. - Assess potential impacts on product quality, compliance, and supply continuity, and ensure appropriate documentation and follow-up in the quality management system. - Own and support lifecycle management of the global Quality Technical Agreement program to ensure alignment with internal policies and applicable regulatory requirements. - Facilitate development, negotiation, execution, and periodic review of Quality Agreements with suppliers and Insmed SMEs. - Monitor agreement status and effectiveness to confirm documents remain current, compliant, and aligned with business and regulatory expectations. - Manage assignment and timely completion of Scorecards and ensure accuracy, appropriate risk allocation, and level of control are established. - Work with the Supplier & Insmed functional SME’s to create corrective action plans to address failures in supplier’s material and services provided. - Trend and analyze supplier performance data to identify systemic risks and improvement opportunities. - Participate in supplier audits as required, including routine, for cause, and qualification audits. - Ensure supplier quality documentation is complete, accurate, inspection ready, and maintained in accordance with company procedures and regulatory expectations. - Assist with development, maintenance, and monitoring of approved supplier list, as well as maintenance of supplier files. - Generate action items from supplier KPI’s for system enhancements and improvements. - Assess potential suppliers for capability, quality systems, and compliance with regulatory and Insmed standards. - Collaborate with procurement, supply chain, functional SME’s and quality assurance teams to evaluate supplier capabilities and performance history. - Maintain supplier escalation programs to ensure that issues are getting elevated to the right levels at Insmed and within the Supplier’s organization. - Adhere to the supplier policies and procedures, as well as global regulations and expectations (e.g. FDA, ISO, etc.) and other duties as assigned. - Assure all supplier quality related quality documentation and records are completed thoroughly and timely to maintain compliance. - Contribute to development and refinement of supplier quality procedures, risk assessment tools, and monitoring frameworks. Qualifications - Minimum of a BS degree in Chemistry, Engineering, Life Science or related discipline. - Minimum of 8 years of relevant Quality Assurance experience of increasing levels of responsibility. - Direct experience in supplier quality management, including qualification, auditing, and performance monitoring. - Demonstrated experience supporting Health Authority inspections and regulatory audits. - Thoroughly knowledgeable on Global drug cGMP's, ISO 13485, and familiar with other Regulatory Requirements. - Direct experience with GMP compliance responsibilities, and Supplier Quality in pharmaceutical and/or medical device products. - Experience with internal and external audits. - Working knowledge of risk management principles and quality system processes. - Excellent communication, negotiation, and influence skills (verbal and written). - Highly proficient in data analytics, critical thinking, and decision-making concepts. - ASQ CQA or similar certification, preferred. Requirements - Up to 10% travel based on vendor requirements. Benefits - Comprehensive medical, dental, and vision coverage and mental health support. - Annual wellbeing reimbursement, and access to our Employee Assistance Program (EAP). - Generous paid time off policies, fertility and family-forming benefits, caregiver support, and flexible work schedules. - 401(k) plan with a competitive company match, annual equity awards, and participation in our Employee Stock Purchase Plan (ESPP). - Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities. - Employee resource groups, service and recognition programs, and meaningful opportunities to connect, volunteer, and give back.