Manager, Quality Assurance - Watertown

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 dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite. · ...

We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite. · ...

We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite. You will play a crucial role in mitigating gaps and risks for all quality and GMP processes, and will run investigations for deviations, change controls, CAPAs ...

+Job Title: · Quality Assurance Associate · Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. · +Support on-the-floor QA issues within the manufacturing suite.Mitigate gaps ...

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

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 ...

Job Title:Quality Assurance Tech · Location: Boston, MA · Duration: 6+ Months- possible extension/conversion · Salary and Other Compensation: · The hourly rate for this position is between $ 35.00/hr- $40 .00/hr . · Factors which may affect pay within this range may include geogr ...

We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite. · ...

We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite.You will play a crucial role in mitigating gaps and risks for all quality and GMP processes. · Support on-the-floor QA issues within the manufacturing suite. · ...

We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite.You will play a crucial role in mitigating gaps and risks for all quality and GMP processes. · ...

We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite. You will play a crucial role in mitigating gaps and risks for all quality and GMP processes. · ...

For over 25 years, Abcam has been providing tools the scientific community needs to enable faster breakthroughs in critical areas like cancer, neurological disorders, infectious diseases, and metabolic disorders. · We believe that to continue making progress, we need to work toge ...

We are seeking a Quality Assurance Manager to oversee our ISO 9001 certified Quality Management System producing research kits and an ISO 13485 and MDSAP certified division producing Class I IVDs ensuring compliance and excellence. · Responsible for the Quality Management Systems ...

We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite.You will play a crucial role in mitigating gaps and risks for all quality and GMP processes, and will run investigations for deviations, change controls, CAPAs, ...

· Title: Director of Quality Assurance CDMO · Location: Greater Boston, MA area · Generous Relocation Assistance provided  · Onsite Presence Required · JOB SUMMARY · The Director of Quality Assurance is responsible for managing all aspects of the Quality Assurance while developi ...

+This organization provides a wide range of diagnostic imaging and laboratory diagnostics... · Develop, document, and execute comprehensive test cases... · ...

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 ...

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 ...