Validation Engineer
Valspec
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 wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals. Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies. VALIDATION ENGINEER Location: Indianapolis, IN (AUTOMATION, INFORMATION & OPERATIONS TECHNOLOGY SOLUTIONS) VALSPEC is looking to identify top tier talent in the areas of automation and computer systems validation and system life cycle management. We are motivated to identify those that share our passion and can mirror the level of energy we put into ensuring that we remain on the cutting edge of the life sciences industry. We are looking for tech savvy professionals with a proven track record in the SDLC (system development life cycle) of automated computer systems within biopharmaceutical environments. Due to our unique approach in meeting the demands of our customers, we are pursuing both individuals that can join our team long term as well as SMEs (subject matter experts) that would like to join us on a consulting basis. Overview This role supports the execution of small projects or portions of larger projects. Supports the generation of quality assurance plans, verification plans, validation plans, and standard operating procedures as well as conduct risks assessments and participate in Quality/Regulatory audits. Develops and executes qualification protocols and final summary reports and may participate in commissioning activities. Requirements 3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience is highly preferred) Experience with automation, commissioning, qualification or operations in a cGMP environment. Direct experience developing validation protocols and execution of protocols. Knowledge of current industry standards such as GAMP5 and ASTM E2500. Tactical thinker with experience working with customers developing testing, validation and/or quality strategies. Excellent client communication skills. Why Join Valspec? At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation. We also offer a highly competitive benefits package, including: Premium medical coverage 401(k) with company match Tuition reimbursement Unique performance incentives And more — all designed to support your growth, well-being, and future. Join a team where your contributions matter, your development is prioritized, and your success is shared. When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @valspec.net. Any other domains are impersonations and should be ignored. Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time. Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established. Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.
- ...small teams in document development and/or execution Qualifications and Experience - Bachelor’s degree in a science or engineering field (or equivalent experience) - 2–4 years’ experience in commissioning and qualification in a regulated industry -...SuggestedFull timeWorldwide
$105.1k - $174.12k
...What Engineering Management contributes to Cardinal Health Engineering is responsible for performing research and analyses to develop... ...within the Engineering function. Responsibilities Lead validation programs across facilities, utilities, equipment, and systems...SuggestedTemporary workWork experience placementLocal areaImmediate startFlexible hours- ...Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&... ...and Experience - Bachelor’s degree (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute...SuggestedFor contractorsWorldwide
$59.95k - $102.62k
...experiences to enhance our collective expertise We are seeking a CQV Engineer to support change control and deviation management activities... ...within pharmaceutical or medical device manufacturing. Validation Engineer / CQV Engineer Responsibilities: Change Control...SuggestedFull timeTemporary workWork experience placement$59.95k - $102.62k
...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 documentation...SuggestedFull timeTemporary workWork experience placementWork at office- A global healthcare solutions provider located in Indianapolis is seeking a Validation Engineering Manager to lead validation programs across facilities, ensuring compliance with FDA and cGMP standards. This role requires 8-12 years of experience, preferably in a regulated...Full time
- Validation Engineering Roles page is loaded## Validation Engineering Roleslocations: Indianapolis, INtime type: Full timeposted on: Posted Yesterdayjob requisition id: R021372BW Design Group is a fully integrated architecture, engineering, construction, system integration...Contract workWork at officeImmediate start
- Sr. Validation Engineer **Who You’ll Work With**When you join Design Group as a Sr. Validation Engineer, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world’s leading companies...Work at officeFlexible hours
- 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...
$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- ...Develop, execute, and document commissioning, qualification, and validation protocols (IQ/OQ/PQ) for new and modified equipment,... ...EMA, and internal quality standards. Coordinate closely with engineering, quality assurance, validation, and operations teams throughout...
- ...Job Description Job Description Integration (Process Validation) Engineer Medical Device Contract Manufacturer – Flexible Films & Packaging Position Summary The Integration (Process Validation) Engineer is responsible for leading and supporting process...Full timeContract workFlexible hours
- A leading engineering solutions provider is seeking a GMP Engineer in Indianapolis, IN. You will plan and execute commissioning and qualification activities for new equipment, ensuring compliance with regulatory standards like GMP and FDA. The ideal candidate has a Bachelor...
- ...0 people worldwide. We provide commissioning, qualification, validation, startup, project management, and other consulting services associated... ...Experience Bachelor’s degree (BS/BA) in Computer Science, Engineering, or related field; equivalent experience may be accepted...Full timeWorldwide
- Barry-Wehmiller Companies Inc. is hiring a Sr. Validation Engineer in Indianapolis, Indiana. This role involves working in a team to solve complex industry challenges, requiring a minimum of 7 years of experience in automation and packaging validation. The ideal candidate...Flexible hours
- ...Description Is this you? Do you enjoy being the go-to Quality Engineering partner for customers and cross-functional project teams? Are you energized by building inspection plans, shaping validation strategies, and transferring NPIs into production smoothly? Do...
$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...- 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...
- 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 and support laboratory instruments,...Part timeCasual workReliefMonday to FridayFlexible hoursDay shift
- A leading pharmaceutical company in Indianapolis is seeking a Principal R&D Engineer to bridge scientific requirements with robust hardware solutions. You will lead verification activities, define test strategies, and ensure compliance with international medical standards...
$71.7k - $79k
$71,700-$79,000 Job Summary: The Manufacturing Engineer is responsible for designing, developing, and optimizing manufacturing... ...molding, assembly, and packaging. Conduct process validation and verification activities to ensure consistent product quality...Work at office- ...Gallup Exceptional Workplace Award, which recognizes the most engaged workplace cultures in the world. Sr. Advanced Manufacturing Engineer - Carmel, IN Reporting to the Advanced Manufacturing Engineering Leader -Finishing, the Sr. Advanced Manufacturing Engineer is...Temporary workH1bFlexible hours
- ...Job Title: Manufacturing Engineer Location: Indianapolis, IN Industry: Manufacturing Job Overview: This position... ...molding, assembly, and packaging. Conducting process validation and verification activities, ensuring consistent product quality...Full timeWork at office
- ...Description: Senior Project Lead Locations: Indianapolis IN. Job Duration: 12 Months (W2) Senior: 8+ years in facilities/utility engineering/AutoCAD/Pharma background. Job Description: Design, troubleshoot, optimize, and maintain utility systems (HVAC, chilled...
$38 - $45 per hour
...Manufacturing Engineer Job Number: 364575 Category: -MFG & Supply Chain SBU Description: Job Title: Manufacturing Engineer... ...Release (PR) certification and support final inspection approval Validate manufacturing readiness and documentation prior to product release...Hourly payLocal areaFlexible hoursShift workAfternoon shift$45 - $60 per hour
...Senior Manufacturing Engineer Job Number: 364352 Category: -MFG & Supply Chain SBU Description: Job Title: Senior Manufacturing... ...Key Responsibilities: Lead development, optimization, and validation of machining processes to support production and program...Hourly payFull timeInterim roleLocal areaShift workDay shift- ...awarded the Gallup Exceptional Workplace Award, which recognizes the most engaged workplace cultures in the world. Manufacturing Engineer - Indianapolis, IN What You Will Do: Responsible for designing, developing, and implementing process engineering...
- ...Manufacturing Engineer Location: Indianapolis, IN Duration: 6+ Months Prepare test procedure/assembly instructions for in-house... ...to manufacturing. Creation of SOP documentation and providing Validation support. Bachelor's degree in Mechanical Engineering, or...
$105.1k - $174.12k
...What Engineering Management contributes to Cardinal Health Engineering is responsible for performing research and analyses to develop... ...within the Engineering function. Responsibilities Lead validation programs across facilities, utilities, equipment, and systems...Full timeTemporary workWork experience placementLocal areaImmediate startFlexible hours$68k - $80k
...analytical solutions, and OneSource services. Job TitleValidation Engineer - Project Farma Location(s) Customer Site - IN Job Description... ...commitment to a Patient Focused and People First mindset. The Validation Engineer I / II is an early-career professional responsible...Full timeWork experience placementWork visa
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