LL01-250919 Manufacturing Execution Systems Validation Specialist (NC) - Morrisville, NC

The Qualification Validation Specialist serves as a Subject Matter Expert (SME) for the Qualification Validation Management (QVM) function within the Quality Assurance (QA) department. · Servir como un experto en materia para el manejo de la validación y calificación dentro del d ...

The Sr. Validations Specialist is accountable for driving results in a fast-paced environment by supporting general pharmaceutical validation of equipment and GxP computerized systems. · ...

The primary responsibility of this role is to provide and lead validation services required for the successful delivery of highly automated warehouse processes and projects. · Provide validation and technical support through the preparation, execution, data analysis, and report w ...

Join an international team working to improve the future of healthcare as a Validation Specialist at Grifols. · Ensure current Good Manufacturing Practices (cGMP) and FDA/Grifols Quality Systems are adhered to throughout the evaluation, review and approval of validation and quali ...

++The Validation Specialist will support the Quality oversight associated with Commissioning & Qualification (C&Q) and validation activities for site. These activities will involve facilities/utilities, equipment/systems, computerized systems, process and validation maintenance, ...

We are seeking a Validation Engineer or Specialist II to perform activities in support of equipment qualification including developing and reviewing protocols and final reports. · ...

Insight Global is seeking an experienced Validation Specialist to lead and execute validation services for a major site expansion project focused on highly automated warehouse and intralogistics processes. · ...

We are seeking an experienced Validation Specialist to support a pharmaceutical client in the Raleigh area. ...

We are seeking an experienced Validation Specialist to support a pharmaceutical client in the Raleigh area. · Provide validation & technical support through the preparation, execution, data analysis,& report writing for IV,Ov&Pv protocols. · Ownership of Change Requests (CR's) re ...

We are seeking a Validation Engineer or Specialist II to perform activities in support of equipment qualification including developing and reviewing protocols and final reports. · Work under general supervision to apply broadening and developing validation expertise · Develop and ...

The primary responsibility of this role is to provide and lead validation services required for the successful delivery of highly automated warehouse processes and projects. · These projects integrate Automated Storage and Retrieval Systems (ASRS), high-density warehouses, automa ...

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? · We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions ...

This is a Hybrid position based out of our RTP, NC Office. · Assists in the development of cGMP operating procedures that relate to process, computer systems, and equipment validation. · ...

Support implementation of a new MES for drug substance manufacturing operations. · ...

The Validation Engineer will perform activities in support of equipment qualification including developing and reviewing protocols and final reports. · Bachelor's Degree in an engineering field while Validation Specialist II requires a Bachelor's Degree in a Scientific Field · ...

As a System Validation Specialist, you have hands on experience with installing, troubleshooting, repairing, calibrating and inspecting monitoring equipment used in healthcare facilities. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:Senior Computer System Validation (CSV) Specialist - with expertise in Manufacturing Execution Systems (MES), specifically Syncade, to support a biologi ...

We are seeking a talented individual committed to work under the highest ethics standards for the position of Senior Computer System Validation (CSV) Specialist - with expertise in Manufacturing Execution Systems (MES), specifically Syncade.We require a dedicated person who can l ...

Primary responsible for quality oversight of GMP documents related to site startup activities. · ...

Senior Computer System Validation (CSV) Specialist - with expertise in Manufacturing Execution Systems (MES), specifically Syncade, to support a biologics manufacturing facility. · ...