Validation Engineer - Indianapolis, IN - Process Alliance

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

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 · ...

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

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. · ...

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 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 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. · ...

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 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) · ...

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 · ...

+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. 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 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. · ...

+Job summary · The Senior Validation Engineer will lead validation efforts to support the Radiopharmaceutical facility and GMP operations in Indianapolis.+Serve as validation subject matter expert for the commissioning and qualification of a 60,000 sq. ft. office, warehouse, and ...

The Validation Engineer II will help support the Radiopharmaceutical facility and GMP operations in Indianapolis. · This is a position that requires working in a GMP cleanroom environment, · wearing protective clothing, and handling of radioactive materials.BMS has an occupancy s ...

+ Job summary: Job Title: · GMP Equipment Validation Engineer – CQV · + Qualifications: Bachelor's degree in engineering, Life Sciences, or related field. · 3+ years of experience in CQV within a GMP-regulated environment. · ...

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. · ...