Average salary: $94,515 /yearly
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- ...OEM Vehicle Validation & Issue Troubleshooting Specialist Onsite, M-F, 8-5 in New Carlisle, IN. Primary Functions: *Vehicle Support: Development powertrain system support and troubleshooting including hardware, software, controls and electronic systems level troubleshooting...Suggested
- ...OEM Vehicle Validation & Issue Troubleshooting Specialist Our client, a Global Power Technology Leader company, is looking for an OEM Vehicle Validation & Issue Troubleshooting Specialist for their New Carlisle, IN location. Responsibilities: Vehicle Support...Suggested
- ...Lead the BMS validation lifecycle across all 8 LMF buildings, from URS authoring through Validation Summary Report and closeout. Author and obtain approval for User Requirement Specifications (URS) for the Metasys BMS platform. Engage JCI on Software Requirement...Suggested
$110k - $130k
...packaging. This role requires a Bachelor of Computer Science and involves responsibilities such as fit gap analysis, documentation for validation of Electronic Batch Records (EBRs), and working in an agile team environment. The position offers a salary range of $110,000-$130...Suggested- ...manufacturing environment supporting advanced vehicle and powertrain validation work. This team works closely with engineering, technicians,... ..., service technician, service writer/advisor, field service specialist, validation technician, or similar technical role. Strong...SuggestedMonday to Friday
- ...Laboratory Systems Validation Specialist I Labcorp is seeking a Laboratory Systems Validation Specialist to join our team at Scicor Drive in Indianapolis, Indiana. Work Schedule Monday through Friday, day shift. Job Responsibilities Technical & Operational Support Operate...SuggestedTemporary workCasual workInternshipMonday to FridayFlexible hoursDay shift
- Current job opportunities are posted here as they become available. MV04-020526 Validation Specialist - Utilities & Facilities (Electrical) Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology...Suggested
- Labcorp is looking for a Laboratory Systems Validation Specialist in Indianapolis, Indiana. This role involves supporting and validating laboratory systems and instruments. Candidates should have a Bachelor’s degree in Clinical Laboratory Science or related field and at...Suggested
- PSC Biotech is seeking a motivated CQV Engineer in Indianapolis, IN to oversee the commissioning, qualification, and validation for facilities and equipment in pharmaceutical and biotech settings. This role is crucial for ensuring project success by supporting validation...Suggested
- ...India. Under a new CEO, *** is committed to a transformative journey with 'Scale @ Speed' as our guiding principle. Job Title: Validation Engineer Location: New Carlisle, IN Onsite/ Hybrid/ Remote: Onsite Job Description: Bachelor's degree in engineering...SuggestedRemote workFlexible hours
- ...Summary: Role: Lead and Validate CNC equipment and related processes used to manufacture medical devices. Focus: Ensure IQ/OQ/PQ, calibration, traceability, and compliance with GMP/ISO standards in a regulated MedTech environment. Aim: Ensure robust, reproducible...Suggested
$75k - $80k
Must Have Technical/Functional Skills • CAD experience in UG NX is a MUST • Proficiency in Product design from concept to production • Experience of generating complex 3D CAD models • Experience in Medical Devices domain • Orthopaedic Product knowledge and design...Suggested- Technical Source is partnered with a leading pharmaceutical manufacturing client in Lebanon, IN supporting a major greenfield facility expansion project. We are seeking a junior-to-mid level CQV / Commissioning Engineer to support execution activities for facility and ...Suggested
$105.1k - $174.12k
...is responsible for strategic oversight and leadership direction within the Engineering function. Responsibilities Lead validation programs across facilities, utilities, equipment, and systems Ensure compliance with cGMP, FDA, USP, and other regulatory standards...SuggestedTemporary workWork experience placementLocal areaImmediate startFlexible hours$80k
Yoh is hiring a Validation Engineer for our Pharmaceutical Manufacturing client in Noblesville, Indiana. Job Functions: Hands on experience or knowledge of Cleaning Visual Inspection, Swabbing and rinse sampling of CIP systems or manufacturing equipment. Support authoring...SuggestedWork experience placement- A leading organization in manufacturing support is seeking a Validation Data Entry professional to join their team in Anderson, IN. This role involves performing inspections, maintaining data accuracy, and supporting manufacturing operations. Ideal candidates will possess...
- ...supporting advanced power, mobility, and digital technology solutions. This team is focused on connected-vehicle capabilities, telematics validation, OTA software updates, and cloud-to-device integration for complex engine and vehicle systems. The environment is technical,...
- Job Description Job Description 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...Worldwide
- ...Job Description Job Description Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a...Immediate start
- ...Sr. Process Validation Engineer Bloomington, Indiana, United States Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products...Full timeContract workTemporary workWorldwideFlexible hoursAfternoon shift
- ...Process Validation Engineer The Process Validation Engineer supports medical device manufacturing by developing, executing, and maintaining validated manufacturing and test processes. The role ensures compliance with FDA QSR (21 CFR 820), ISO 13485, and cGMP requirements...Work at office
- ...by filling resource gaps, ensuring projects remain on track during critical milestones. Document and support Computer Systems Validation (CSV) tasks as needed to meet regulatory requirements. Bachelor's degree in Engineering, Science, or related field. Experience...
- Validation Engineering Roles page is loaded## Validation Engineering Roleslocations: Indianapolis, INtime type: Full timeposted on: Posted... ...impact. You'll work alongside seasoned leaders, technical specialists, and subject matter experts within our Regulatory Compliance...Contract workWork at officeImmediate start
- E Solutions, LLC seeks a Validation Engineer in Indianapolis, IN to manage commissioning and qualification activities for new equipment. Candidates require a Bachelor's degree in a relevant field and at least five years of experience in a regulated environment. The role...
- A leading engineering firm in Indianapolis is looking for Validation Engineers to support capital project CQV delivery in the Life Sciences industry. This role involves developing validation and compliance documents, managing client relationships, and leading project execution...
- ...Description Job Description Valspec—a global provider of system validation and lifecycle services—provides commissioning and... ...that also includes computer system validation engineers and specialists. Key Responsibilities: Lead and execute CQV activities for...Immediate start
- ...obsessed with how it will be done. Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project schedules - Track and...For contractorsWorldwide
$59.95k - $102.62k
...engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise Validation/CQV Engineer Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation...Temporary workWork experience placementWork at office$59.95k - $102.62k
...change management, deviation investigations, and CQV lifecycle support within pharmaceutical or medical device manufacturing. Validation Engineer / CQV Engineer Responsibilities: Change Control Management Author, review, and manage change controls impacting systems...Temporary workWork experience placement$144.7k - $261.3k
...Job Description The Senior ML Validation Research Engineer will lead applied machine learning research focused on improving verification and validation of ML components used in robotics and autonomous driving systems. This role centers on simulation-based evaluation...Local areaWork from homeFlexible hours


