Senior Quality Engineer - Easton

We are seeking a Quality Engineer to handle quality management systems including document control, regulatory, sterilization coordination, CAPA, and risk management activities related to design, development, manufacturing, · distribution of medical devices.Ensure compliance to QS ...

The Quality Engineer will support and maintain the Quality Management System (QMS) in a regulated medical device environment.This role is responsible for activities including document control, · regulatory compliance, · sterilization coordination, · CAPA, · risk management, · Aud ...

Becoming a Quality Engineer at System One. · We help clients get work done more efficiently and economically without compromising quality. · ...

Description · Primary Duties & Responsibilities · Program manage the ISO Internal audit program for SiC, LLC USA operations · Organize and perform ISO Internal audit-related and GRR metrology alignment program activities to maintain and improve our processes, metrology systems an ...

· Job Title: Lead Quality Engineer · Job Code: 33131 · Job Location: Northampton, MA · Schedule: 9/80 · Job Description: · The Lead Quality Engineer leads the execution of Quality activities for large developmental, production, and aftermarket contracts. They will also develop ...

Job Description · Position:    Quality Assurance Engineer - Corporate  · Location:    Victaulic Corporate Headquarters - Easton, PA · Reports To:  Quality Assurance Supervisor · **RELOCATION PACKAGE IS OFFERED FOR THIS ROLE** · About Us: · Victaulic is a global leader in mechanic ...

Job Description · Primary Duties & Responsibilities · Program manage the ISO Internal audit program for SiC, LLC USA operations · Organize and perform ISO Internal audit-related and GRR metrology alignment program activities to maintain and improve our processes, metrology system ...

Linde is seeking a Senior Quality Engineer to ensure process control system aligns with advanced technology semiconductor customers. · ...

Primary Duties & Responsibilities · Program manage the ISO Internal audit program for SiC, LLC USA operations · Organize and perform ISO Internal audit-related and GRR metrology alignment program activities to maintain and improve our processes, metrology systems and related docu ...

The Quality Engineer plays a key role in supporting the organization's Quality Management System with a primary focus on design quality and design controls while also contributing to other Quality activities across the product lifecycle. Provide Quality Engineering support with ...

The Quality Engineer plays a key role in supporting the organization’s Quality Management System with a primary focus on design quality and design controls while also contributing to other Quality activities across the product lifecycle This position supports compliance with ISO ...

The Quality Engineer is responsible for supporting quality assurance efforts across product development, manufacturing and customer-facing issue resolution. · ...

The Quality Engineer plays a key role in supporting the organization's Quality Management System, with a primary focus on design quality and design controls, while also contributing to other Quality activities across the product lifecycle. · This position supports compliance with ...

Job Summary · The Quality Engineer is responsible for supporting quality assurance efforts across product development, manufacturing, and customer-facing issue resolution. This role partners with engineering, operations, sourcing, and commercial teams to ensure quality standards ...

This Quality Engineer role will ensure that all products meet established standards of safety, reliability, and performance. · Support new product development projects by managing quality deliverables such as past performance analysis, FMEAs, and first-part approvals. · Investiga ...

The Quality Engineer plays a critical role in supporting qualification activities to ensure compliance with cGMP standards and internal procedures for sterile injectable IV bag products at a newly established greenfield pharmaceutical manufacturing facility. · ...

The Quality Engineer is responsible for adhering to the Quality Management System which includes identifying and complying with ISO compliant activities, employing LEAN processes, · and coordinating assessment activities with 3rd parties.The Quality Engineer demonstrates strong w ...

The Quality Engineer demonstrates strong working-knowledge of quality control processes, ISO and LEAN concepts, industrial technical concepts, excellent data management skills, and the ability to lead cross-functional teams.* Support and performs detailed evaluations and inspecti ...

The Manufacturing Quality Engineer supports the effective implementation and continuous improvement of the Quality Management System (QMS) within a manufacturing environment. · ...

This internship offers an exciting opportunity to gain hands-on experience in a collaborative, fast-paced production environment. · ...