6115 - Senior CSV Engineer / Senior Validation Engineer - Indianapolis

We are currently in search of a Validation Engineer for a pharmaceutical manufacturing client in the Greater Indianapolis Area. · ...

We're hiring a Validation Engineer to support Computer System Validation (CSV) and system qualification activities in a regulated pharmaceutical environment. · BS or MS in Engineering preferred · Kneat experience required · ...

This engineer will go through a series of CQV within an FDA regulated environment for a pharmaceutical customer. · ...

We are seeking an experienced Equipment Validation Engineer to support validation efforts across our cGMP manufacturing and laboratory operations. · ...

We are seeking experienced DeltaV Designers with a strong pharmaceutical manufacturing background to support a greenfield pharmaceutical facility buildout.This is a hands-on design-focused role responsible for developing DeltaV control system designs from early project phases thr ...

We are seeking an experienced Equipment Validation Engineer to support validation efforts across our cGMP manufacturing and laboratory operations. · This is a contract role with strong potential for extension. · ...

We're hiring a Validation Engineer to support Computer System Validation (CSV) and system qualification activities in a regulated pharmaceutical environment. · ...

CSV Engineer to support validation and qualification of laboratory analytical instruments in a GMP environment. · ...

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. · ...

Valspec—a global provider of system validation and lifecycle services—is looking to identify top tier talent in the areas of automation and computer systems validation and system life cycle management. · ...

We are seeking an experienced Validation Engineer to support validation efforts across our manufacturing and laboratory operations. This role offers the opportunity to contribute to high-impact projects in a regulated environment focused on therapeutic production. · ...

CQV Engineer: Lead deployments and Commissioning & Qualification efforts of robotic systems in multi-disciplinary teams within manufacturing sites, quality, and other business units. · Work with vendors to solve FAT and SAT activities. · Develop capabilities in robotics and PLC p ...

We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience. · Develop documentation for CQV activities · Write and execute protocols (field verification) · ...

+Job summary · Work your magic with us... · +ResponsibilitiesEstablish and justify cleaning processes for new/modified equipment and clients. · Serve as the site SME for cleaning-related deviations and CAPAs. · ...

The Senior Validation Engineer will lead validation efforts to support the Radiopharmaceutical facility and GMP operations in Indianapolis.This role is responsible for the development, execution, and management of commissioning qualification ,and validation documents and protocol ...

This role is responsible for leading validation efforts to support the Radiopharmaceutical facility and GMP operations in Indianapolis. · The Senior Validation Engineer will develop, execute and manage commissioning qualification documents protocols for highly specialized facilit ...

+h2>Job summary · As a global leader in industrial automation, process control solutions and instrumentation, we serve clients in the life sciences, pharmaceutical, medical device, food & beverage, and utilities sectors... · ...

The Validation Engineer II will help support the Radiopharmaceutical facility and GMP operations in Indianapolis. The position will utilize a wide range of engineering disciplines to support the advancement from construction to clinical development and subsequent GMP commercial o ...

We are looking for a Validation Engineer to join our team in Indianapolis. The successful candidate will be responsible for establishing and maintaining validated cleaning processes for equipment and processes supporting existing and new clients. · ...

We are seeking a detail-oriented and proactive Validation Engineer II for our Indianapolis office to support compliance and efficiency in a regulated environment.This role is responsible for executing and managing periodic reviews of computer systems. · Create technical documents ...

The Validation Engineer II will help support the Radiopharmaceutical facility and GMP operations in Indianapolis. · This is work that transforms lives of patients, and careers of those who do it.Take your career farther than you thought possible. · ...