Sr Validation Engineer - Indianapolis, IN

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 · ...

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

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

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—is looking to identify top tier talent in the areas of automation and computer systems validation and system life cycle management. · ...

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. · 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. · ...

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 ...

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

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. · ...

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) · ...

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 ...

We are seeking a highly motivated · and detail-oriented GMP Equipment Validation Engineer · to support Commissioning, · Qualification, · and Validation (CQV) activities · Clean steam generators · HVAC systems · ...

The Validation Engineer II will support the Radiopharmaceutical facility and GMP operations in Indianapolis. The position will involve drafting and executing commissioning, qualification, and validation (CQV) documents and protocols for highly specialized facility equipment. · ...

· The Senior Validation Engineer will lead validation efforts to support the Radiopharmaceutical facility. · This role is responsible for developing commissioning qualification documents protocols for highly specialized equipment facilities utility analytical process equipment. ...

+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 Validation Engineer II will help support the Radiopharmaceutical facility and GMP operations in Indianapolis. · Work with the project team and/or General Contractor as required to support the commissioning and validation of a 60,000 sq. ft. office, warehouse, and GMP Radiopha ...

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 ...

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 ...