Quality Assurance Associate - Cambridge, MA

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 ...

++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 ...

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 ...

The QA Associate will help ensure that life-changing biopharmaceutical products are manufactured to the highest standards. · Provide raw material support · Deliver on-the-floor QA support to manufacturing · ...

This position involves reviewing event documentation such as batch records and regulatory filings. · ...

This is a Quality Assurance Associate II position in the pharmaceutical industry. · ...

The Quality Assurance Associate II will review event documentation and support design development plans. · Knowledge of relevant government regulations. · Understanding of ICH,GLP,Congener requirements. · ...

+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 ...

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 ...

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. · ...

KPMG is currently seeking an Senior Associate to join Technology Assurance - ERP Control in our Audit practice. We are known for being a great place to work and build a career, KPMG provides audit, tax and advisory services for organizations in today's most important industries. ...

The Associate, Third Party Assurance supports FLOD Third Party Risk Management in working with business units to ensure third-parties are managed in accordance with the TPRM program. This function performs due diligence activities including data governance, cyber security and ope ...

+ Job summary: Associate Director Quality Assurance · Rapport Therapeutics is seeking an Associate Director of Quality Assurance to lead quality assurance activities across both quality systems and GMP-focused operations. · + Responsibilities:Support quality oversight in a phase- ...

Santander is a global leader and innovator in the financial services industry and is evolving from a high-impact brand into a technology-driven organization. · ...

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. · ...

+Job summary · The Senior Manager, Quality Assurance, will be a key member of the Quality team, leading quality assurance activities across both quality systems and GMP-focused operations to support the advancement of global Phase 3 clinical trials for RAP-219 and other assigned ...

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, ...

Ensure compliance with Good Clinical Practice (GCP), Good Clinical Laboratory Practice (GCLP), and related regulatory standards across MBX's clinical and nonclinical programs. · ...