Top Tech Jobs & Startup Jobs in Boston, MA

Responsible for reviewing and processing Product Quality Complaint records, ensuring compliance with regulations, and analyzing complaint trends.

Draft and manage complex contracts and budgets, ensure adherence to processes, train team members, and engage with clients as needed.

The GVP Auditor will lead clinical auditing projects, ensuring compliance with GCP and GVP guidelines, and provide consulting services to clients while promoting quality improvements.

The Freelance GCP Auditor will conduct audits, develop Quality Management Systems, draft SOPs, and provide GxP compliance consulting.

Develop R programming code for clinical trial data analysis, visualization, ensuring data quality, compliance, and providing training to programmers.

The eQMS Specialist supports the Electronic Quality Management System through document management, training coordination, system administration, and report processing.

The Workday PSA Administrator is responsible for technical support and maintenance of Workday PSA configurations, processing service desk tickets, collaborating on improvements, and leading projects to optimize system functionalities.

Manage cross-functional teams for IVDR compliance, monitor regulatory applications, and facilitate product launches and approvals.

The GMP Auditor is responsible for conducting GMP audits, acting as a Subject Matter Expert, and ensuring regulatory compliance in aseptic processing within client organizations.

Manage and oversee project planning, delivery, and communication from initiation to implementation, while identifying risks and facilitating meetings.