Supervisor, Quality Assurance - Medford, MA

Global Clinical Submissions Quality Lead to support the Tanezumab submission: quality lead develops, oversees and executes strategies and plans to ensure that clinical data included in the Tanezumab submission to regulators are complete and accurate and meet global regulatory req ...

We are seeking a Global Clinical Submissions Quality Lead to support Business Development Due Diligence activities: quality lead will review external clinical data and ensure that clinical data included on due diligence packages are complete and accurate and meet global regulator ...

The position involves leading quality assurance for vaccine clinical submissions to regulators. · ...

The Quality Assurance Principal supports DeepHealth products and product development along with the Quality Management System throughout the organization. · Actively engage cross-functionally within the organization. · Act as the Quality lead for design changes to existing DeepHe ...

+The Quality Assurance Principal is responsible for supporting · +Actively engage cross-functionally within the organization, such as with the Engineering, Clinical and Marketing teams, to develop new products within the Product Lifecycle Management (PLM) and New Product Introdu ...

The Quality Assurance Specialist supports DeepHealth products and product development, collaborating cross-functionally to guide product development. · The Quality Assurance Specialist works within the team to support Quality processes such as QMS training and CAPA management.The ...

The Quality Assurance Principal is responsible for supporting DeepHealth products and product development.. · Actively engage cross-functionally within the organization to develop new products. · Ensure compliance with applicable standards and guidances. · ...

The Quality Assurance Specialist will actively contribute to the implementation and maintenance of the Quality Systems Manual and conduct GMP compliance audits as directed. The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical Tria ...

We are seeking a highly skilled Quality Assurance Manager to support commercial finished goods operations and external manufacturing partners. · ResponsibilitiesServe as the primary QA representative for commercial finished goods and external manufacturing partners. · ...

The QA Manager serves as the Quality Assurance representative for commercial finished goods and external manufacturing partners. This role oversees quality activities related to finished goods assembly labeling packaging and serialization to ensure compliance with internal standa ...

The Quality Assurance Associate will review event documentation, production records, and support design development plans. · ...

You could be the one who changes everything for our 28 million members as a Customer Care professional at Centene. We endeavor to craft a better human experience by transforming from a company perspective to a customer perspective. · ...

The Quality Assurance Associate will review event documentation, production records and support design development plans. They will also be involved in device development projects and have a good understanding of FDA and EMA regulations. · Review of event documentation such as Ba ...

Review of event documentation such as Batch records Exceptions and Regulatory filings Production record review and Product disposition for drug substance drug product device assembly and finished goods Support design development plan including design verification and DHF delivera ...

The QA Manager serves as the Quality Assurance representative for commercial finished goods and external manufacturing partners.This role oversees quality activities related to finished goods assembly labeling packaging and serialization to ensure compliance with internal standar ...

++Review event documentation such as Batch records Exceptions and Regulatory filings Production record review and Product disposition for drug substance drug product device assembly and finished goods+ · +Minimum BS degree in life sciences engineering or related field Minimum of ...

Duties include review of event documentation such as Batch records, Exceptions and Regulatory filings with production record review and Product disposition for drug substance device assembly and finished goods. · Skills required are knowledge of relevant government regulations ag ...

We are seeking a highly skilled Quality Assurance Manager to support commercial finished goods operations and external manufacturing partners.This role plays a critical part in ensuring product quality, regulatory compliance, and operational excellence across global commercial su ...

Manage quality aspects of commercial finished goods specifications at CMOs for global commercial supply. · ...

The Quality Assurance Engineer will support and participate in the daily testing and quality assurance activities for technology projects within the Fidelity Small Market Payroll business unit. · Plan, design and execute test strategies for small and medium projects... · ...