Validation Engineer - Indianapolis, IN

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

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

We are seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in 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 seeking an experienced Equipment Validation Engineer to support validation efforts across our cGMP manufacturing and laboratory operations. · ...

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

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

Are You Ready? · CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational readines ...

Role: Validation Engineer – Equipment & CSV (GMP Environment) · Location: Indianapolis, IN · Onsite · Job Description: · Author equipment qualification and validation packages · Plan coordination with equipment manufacturer or supplier for preventative maintenance · Technical r ...

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. · ...

PACIV stands for Process Automation, Controls, Instrumentation, and Validation. · 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 sect ...

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 ...

· Job Description · Job Title: Verification and Validation Engineering Specialist · Working Pattern: Full-Time · Working location: Indianapolis, IN/Hybrid - 3 Office Days/Week · We're looking for a Verification and Validation Engineering Specialist to join our growing team. This ...

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. · ...

Job summary · RayzeBio seeks a Validation Engineer II to support Radiopharmaceutical facility and GMP operations in Indianapolis. · ...

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 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 ...

We are seeking a full-time Level I Validation Engineer/Specialist to join our teams in Indiana. This role will provide an opportunity for professional development, implementation of new services, and cultivation of new geographical areas. · The ideal candidate will have a strong ...

+ 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. · ...