11 results for Validation Engineer Jobs in Des Plaines, IL, US

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 co...

The Validation Engineer is responsible for preparing, drafting, and executing validation protocols, validating automated manufacturing equipment, drafting validation change requests, executing validation tests, and documenting activities. They will also support process development activities and com...

Responsible for validating pharmaceutical packaging equipment, including composing and executing validation protocols, managing change controls, monitoring project progress, and ensuring compliance with FDA standards. Will lead projects, conduct investigations for improvements, and coordinate vendor...

Job SummaryThis position is responsible supporting the Validation Department to commission, qualify and decommission pharmaceutical packaging equipment. They will lead, manage, and support a variety of on-going projects for clients in the pharmaceutical industry related to packaging engineering. Pos...

LHH Recruitment Solutions has partnered with a growing organization, and they are seeking a motivated Validation Engineer to join their team in Lincolnshire, IL. You will play a crucial role in ensuring the safety, quality, and compliance of the company's products and processes. The ideal candidate ...

Unlock your potential as a Validation Engineer with my client, a leading player in the healthcare industry. In this dynamic role, you'll spearhead the oversight, evaluation, and calibration of equipment, ensuring safety, quality, and purity standards. Your impact will resonate through maintaining co...

Job SummaryResponsible for leading design validation activities as part of product development initiatives across a wide variety of product categories. This role involves planning, executing, and reporting on design validation efforts. Collaborate with multiple product divisions and cross-functional...

Responsibilities: Strong understanding of regulations and guidance related to Computer System Validation principles and Quality Management Systems (21CFR Part 11, GAMP- 5, EU Annex 11 and other relevant regulations). Bachelor's degree or equivalent experience in computer science, information technol...

Nemera is a world leader in the design, development, and manufacturing of drug delivery devices for the pharmaceutical, biotechnology, & generics industries. With locations worldwide, some of our services and products include eyedroppers, pumps, valves, inhalation devices, airless dispensers, an...

ResponsibilitiesStrong understanding of regulations and guidance related to Computer System Validation principles and Quality Management Systems (21CFR Part 11, GAMP- 5, EU Annex 11 and other relevant regulations). Bachelor's degree or equivalent experience in computer science, information technolog...