Quality Assurance Specialist

3 weeks ago


Boston, Massachusetts, United States PSG Global Solutions Careers Full time

We're seeking a Quality Assurance Specialist to facilitate the authoring of effective Standard Operating Procedures (SOPs) and Working Practice Documents (WPDs) in a pharmaceutical and medical products industry setting.


Key responsibilities include managing the change request, deviation, and periodic review processes of procedural documents. Additionally, the successful candidate will assist in the assessment and implementation of Quality Standards in R&D and facilitate the implementation of external regulatory changes in the appropriate procedural documents.


The ideal candidate will have 8+ years of hands-on experience in the pharmaceutical/biotech industry, with a focus on R&D functions such as Clinical, Regulatory, Pharmacovigilance, etc. Proven experience in Procedural Document Lifecycle Management within a R&D Quality Management System, including document workflow utilizing a Controlled Document Management System, is also required.


As a Quality Assurance Specialist, you will proactively manage change by identifying opportunities and coaching self and others through the changes. If you have a passion for quality and a drive to succeed in a dynamic industry, we encourage you to apply for this exciting opportunity.



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