CQV / CSV Specialist - Greenville, NC

We are seeking an experienced and technically strong CQV / CSV Specialist with a primary focus on Automation and Manufacturing Systems to support FDA-regulated manufacturing operations at a client site in Greenville, North Carolina. · This is a 4 month contract position with stro ...

Job summaryThis role is CSV and automation-focused, working directly with the client's automation and manufacturing systems teams. · ...

We are seeking an experienced and technically strong CQV / CSV Specialist with a primary focus on Automation and Manufacturing Systems to support FDA-regulated manufacturing operations at a client site in North Carolina. · ...

We are seeking an experienced and technically strong CQV / CSV Specialist with a primary focus on Automation and Manufacturing Systems to support FDA-regulated manufacturing operations at a client site in North Carolina. · Lead and execute Computer System Validation (CSV) and aut ...

Job summary · V&EG busca un especialista CQV/CSV con experiencia en automatización y sistemas de manufactura para apoyar operaciones FDA-reguladas en Carolina del Norte. · Lidera y ejecuta actividades de validación CSV y automático para sistemas de manufactura. · ...

We are seeking an experienced and technically strong CQV / CSV Specialist with a primary focus on Automation and Manufacturing Systems to support FDA-regulated manufacturing operations at a client site in North Carolina. · This role is CSV and automation-focused, working directly ...

Validation & Engineering Group, Inc. (V&EG) is seeking an experienced CQV / CSV Specialist to support FDA-regulated manufacturing operations in North Carolina. · ...

Insight Global is looking for a CSV Engineer for a pharmaceutical client in Greenville. · Assist in resolving protocol execution issues using critical analysis and develop sound reasonable solutions/li> ...

The job requires extensive experience with IQ,OQ,PQ protocols development and execution, · Validation using V-model in previous positions and is now using the Agile/waterfall methodology. · Good experience in using Risk Based approach to validate configured and custom developed s ...

We are seeking a highly skilled Validation Analyst or CQV/CSV Engineer to support sterile manufacturing lines and site-wide change management. · ...

We are seeking a highly skilled Validation Analyst or CQV/CSV Engineer to support sterile manufacturing lines and site-wide change management.The successful candidate will be responsible for the full validation lifecycle within GxP environments. · You will utilize a risk-based ap ...

We are seeking an experienced Validation Analyst / CQV / CSV Engineer to support Steriles Manufacturing operations within a regulated GxP pharmaceutical environment. · Develop, execute and document Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qu ...

We are seeking an experienced Validation Analyst / CQV / CSV Engineer to support Steriles Manufacturing operations within a regulated GxP pharmaceutical environment. · Develop, execute, and document Installation Qualification (IQ), Operational Qualification (OQ), and Performance ...