Top Tech Jobs & Startup Jobs in Boston, MA

As a Regulatory Affairs Leader, you will manage pre/postmarket regulatory submissions, ensure compliance, train staff, and liaise with regulatory bodies. Responsibilities include preparing reports, addressing inquiries, and improving quality systems.

The Project Engineer will lead design and development for DVT prevention devices, managing projects and collaborating across disciplines to ensure compliance with medical safety standards.

The Data Specialist is responsible for tracking and verifying data entry for batch records to ensure accuracy in the GMP documentation process while providing data analysis support for reporting.

Manage the Marketing team’s purchase orders and invoices, maintain expense trackers, and support budget reconciliation processes. Requires advanced MS Excel and customer service skills.

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

The role involves researching and writing state-specific business and corporate resources, requiring a J.D. and significant experience in corporate transactions.

Support the marketing teams by managing budgets, processes, and tools, alongside conducting research and handling assigned projects.

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

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

Design and develop applications using .NET. Lead a team of developers through the software lifecycle, manage priorities, and adapt to new technologies.