Top Pharmaceutical QA & Test Engineering Jobs in Boston, MA

The Design Quality Engineer II will support quality functions in design assurance for medical devices, ensuring compliance with regulatory standards, conducting risk assessments, and analyzing quality metrics.

Lead quality control analysis, overseeing chemistry and biochemistry programs, training staff, developing formulations, and ensuring compliance with regulatory standards.

The Engineering Specialist, Quality develops quality assurance processes for medical devices, ensuring regulatory compliance and risk management throughout the product lifecycle.

The Quality Control Systems Engineer oversees LabVantage LIMS, leading enhancements and validations, ensuring compliance and effective system operations in a regulated environment.

The Senior Manager, QA - Commercial GMP oversees Quality Assurance for drug manufacturing, ensuring GMP compliance and leading quality initiatives. They support audits, product lifecycle management, and continuous improvement, while mentoring QA teams and integrating digital tools into processes.

The Lead QA Automation Engineer will design and implement automation frameworks, mentor junior engineers, and collaborate with teams to ensure software quality in an Agile environment.

As a Supplier Quality Senior Engineer, you will oversee supplier compliance with quality regulations, lead issue resolution, and perform supplier assessments to ensure quality in healthcare products.

Serve as a CQV subject-matter expert and discipline lead providing strategic CQV consulting, client and project oversight across multiple sites, business development, mentorship, and technical guidance on commissioning, qualification, validation, QRM, automation integration, and digital validation strategies.

Develop and maintain automation test plans and frameworks, integrate testing into CI/CD, and drive quality improvements collaboratively with teams.