Quality Auditor - Bristol

We are seeking a Quality Auditor to join our team at Eaton's IS AER FED facility in Rumford RI. · eaton is a premier manufacturer in the aerospace industry servicing commercial and military markets. · The quality auditor will work from prints method sheets inspection method sheet ...

Eaton's IS AER FED is currently seeking a Quality Auditor - 2nd Shift. · This position requires use of information or access to hardware which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. · ...

Eaton is seeking a Quality Auditor - 2nd Shift at our Rumford, RI facility. · ...

The Quality Process Auditor performs first piece inspections and monitors the machining assembly and testing operations to assure that products comply with specifications. Responsibilities include performing nightly audits of all cells publishing nightly reports identifying oppor ...

This position is responsible for ensuring product meets Silgan, Slatersville customer specifications. · ...

The Quality Process Auditor performs first piece, in-process and finished product inspections. They monitor the machining, assembly and testing operations to assure that the products comply to their specifications and perform incoming inspections as needed. · ...

The Quality Process Auditor performs first piece, in-process and finished product inspections. · ...

This is an on-site position in North Kingstown, RI. · ...

Job Title: Documentation Specialist II · Invagen Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist.The Documentation Specialist is responsible for the creation and revision of new and existing GMP batch production records as well ...

People Incorporated is seeking an accomplished Chief Financial Officer. · ...

+We are partnered with our growing pharmaceutical packing client that is looking to expand their leadership team. · This role is focused on the oversight and safety of their manufacturing activities in the respective section to ensure activities carried out are as per requirement ...

InvaGen Pharmaceuticals is searching for an experienced Manufacturing Validation Engineer. The role involves creating and revising GMP documents, preparing qualification & validation documents of equipment and computer systems. · Develops appropriate disposition metrics · Creates ...

The Packaging Manager is responsible for overseeing the packaging process to ensure quality and efficiency. · Monitor and control planned production to meet packaging targets and quality standards. · Review planned production vs. actual production daily and control the production ...

InvaGen Pharmaceuticals is searching for experienced candidates for the position of Manufacturing Validation Engineer. · ...

+p>Control manufacturing activities in the respective section to ensure activities carried out are as per requirement of cGMP & safety to meet the quality and manufacturing targets in time.+ul>+li>Monitor and control planned production by daily activity review as per production p ...

The Section Head position involves controlling manufacturing activities in the respective section to ensure compliance with cGMP & safety standards. Key accountabilities include monitoring production schedules, ensuring availability of raw materials, and implementing quality cont ...

The content and statements documented in this job description are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. · Develops appropriate d ...

Monitor production to meet targets and quality standards by daily activity review as per packaging plan. · Review production schedule vs actual production daily. · Prepare production schedules for blocks. · ...

This role works in cGMP laboratory or manufacturing environment where personal protective equipment is required. · The Section Head will be responsible for controlling manufacturing activities to ensure they meet quality and packaging targets on time. · ...

Control manufacturing activities in the respective section to ensure activities carried out are as per requirement of cGMP & safety to meet the quality and manufacturing targets in time. · ...

Saab is seeking a driven and collaborative Lead Supplier Quality Engineer to join our team in Bristol, RI. · ...