Top Tech Jobs & Startup Jobs in Boston, MA

The Project Portfolio Manager will oversee multiple projects related to cGMP manufacturing equipment and renovations, requiring extensive capital project management expertise and cross-functional collaboration.

The Technical Writer will create documentation for network hardware, user guides, and design specs, collaborating with product management and engineering teams.

The role involves using AutoCAD to create diagrams and facility drawings while adhering to CAD standards.

Provide phone and desktop support while resolving issues, deploying computers for new hires, and collaborating with support groups.

Manage regulatory affairs by preparing, reviewing, and auditing medical device documentation, including Technical Files and Risk Management files.

The Software Engineer will write code/UI, troubleshoot with stakeholders, and maintain Windows Services with strong debugging skills and memory management knowledge.

The Technical Document Writer will draft and maintain cGMP documentation, collaborate with teams, and ensure compliance with quality regulations.

Lead the complaint investigation process, engage with product design, ensure compliance with MDR, and report on quality metrics.

Develop and support Linux delivery pipelines, manage servers, automate testing, and contribute to monitoring efforts using NewRelic.

The Regulatory Affairs Specialist will oversee regulatory submissions, ensure compliance with regulations, and support clinical studies while liaising with regulatory agencies and internal teams.