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Validation Manager Jobs in Indiana (NOW HIRING)

Voto Consulting LLC

Validation Engineer

Lebanon, IN · On-site

Position- Senior Validation Engineer, Local Type- ONSITE Location- Lebanon, IN Visa- GC Key ... management, and integrated building systems. * Develop control sequences, points lists, network ...

Valspec

Validation Engineer

Indianapolis, IN

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... cycle management. We are motivated to identify those that share our passion and can mirror the ...

Guidehouse

Model Validation Lead

Indianapolis, IN · On-site

Advise clients on model risk management, AI governance, and responsible AI practices * Mentor ... Experience validating ML, statistical, and predictive models in regulated or highrisk environments

Verista, Inc.

Validation Engineer 2

Fishers, IN · On-site

Design validation plans. Conduct independent verification of testing against specifications ... Support clients change management program - including author proposed changes, execute impact ...

Verista, Inc.

Validation Engineer 2

Fishers, IN · On-site +1

$95.39K - $153.50K/yr

Design validation plans. Conduct independent verification of testing against specifications ... Support clients change management program - including author proposed changes, execute impact ...

Verista, Inc.

Validation Engineer 2

Fishers, IN · On-site +1

$95.39K - $153.50K/yr

Design validation plans. Conduct independent verification of testing against specifications ... Support clients change management program - including author proposed changes, execute impact ...

Trimedx

Inventory Validation Technician

Indianapolis, IN · On-site

$18.49/hr

The Inventory Validation Technician works as a part of an inventory validation team and provides clinical equipment services under the close supervision of TRIMEDX management. Duties include, but are ...

CAI

Validation Engineer

Indianapolis, IN · On-site

$72.80K - $80.10K/yr

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

Novartis

Process & Validation Expert

Indianapolis, IN

$97.60K - $146.40K/yr

As the Process & Validation Expert, you will execute and manage process, primary packaging, and cleaning validation activities and change management activities to meet cGMP requirements on time and ...

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See Indiana salary details

$45.2K

$100.3K

$152.7K

How much do validation manager jobs pay per year?

As of May 30, 2026, the average yearly pay for validation manager in Indiana is $100,309.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,900.00 and $125,600.00 per year, depending on experience, location, and employer.

What Is a Validation Manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

What are the key skills and qualifications needed to thrive as a Validation Manager, and why are they important?

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

How does a Validation Manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What are Validation Managers?

Validation Managers are professionals responsible for overseeing and managing the validation processes within an organization, particularly in industries like pharmaceuticals, biotechnology, and manufacturing. Their main role is to ensure that products, equipment, and processes meet regulatory standards and operate consistently as intended. They coordinate validation activities, develop protocols, lead teams, and ensure compliance with quality and safety regulations. Validation Managers play a critical role in maintaining product quality, reducing risks, and ensuring that all procedures meet industry and governmental standards.

What is the role of a validation manager?

A validation manager oversees the process of ensuring that products, processes, or systems meet specified requirements and quality standards. They develop validation protocols, coordinate testing activities, and ensure compliance with industry regulations, often working with quality assurance teams and utilizing validation tools. Their role is critical in industries like pharmaceuticals, manufacturing, and healthcare to ensure safety and efficacy.

What is the difference between Validation Manager vs Quality Assurance Specialist?

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

More about Validation Manager jobs
What are the most commonly searched types of Validation jobs in Indiana? The most popular types of Validation jobs in Indiana are:
What are popular job titles related to Validation Manager jobs in Indiana? For Validation Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Validation Manager jobs in Indiana look for? The top searched job categories for Validation Manager jobs in Indiana are:
What cities in Indiana are hiring for Validation Manager jobs? Cities in Indiana with the most Validation Manager job openings:
Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Indiana as of May 2026, with employment types broken down into 17% As Needed, and 83% Full Time. Highlights an 67% Physical, and 33% Hybrid job distribution, with an average salary of $100,309 per year, or $48.2 per hour.

Validation Lead

Novartis Pharmaceuticals Corporation

Indianapolis, IN

$114.10K - $211.90K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 15 days ago

Job description

Band

Level 4


Job Description Summary

Bring your expertise to a role where your decisions directly safeguard product quality, patient safety, and regulatory trust. As our Validation Lead in Indianapolis, you will shape and own the site's end to end validation strategy-process, cleaning, primary packaging, and ongoing process verification-so manufacturing stays inspection ready and continuously compliant with current Good Manufacturing Practice. You'll partner closely with Manufacturing Science and Technology, Engineering, Information Technology, Quality Control, and Analytical Science and Technology to orchestrate the Validation Master Plan, monitor meaningful performance indicators, and proactively manage risk. Your work will also enable smooth product transfers and launches by generating robust, data driven evidence for registration dossiers. If you thrive on building clear standards, coaching teams, and turning complex technical challenges into practical, reliable solutions, this role gives you the platform to make an impact that matters.
#LI-Onsite
Location: Indianapolis, IN
Relocation Support: Yes


Job Description

Key Responsibilities:

  • Develop and implement site validation strategies for process, cleaning, packaging, and ongoing process verification.
  • Oversee the Validation Master Plan, ensuring timely execution and audit readiness.
  • Provide technical expertise and guidance for risk assessments and validation documentation.
  • Lead validation activities, ensuring compliance with Novartis and regulatory requirements.
  • Partner with cross-functional teams to support equipment, utilities, and analytical method qualification.
  • Facilitate product transfers and launches by aligning validation approaches and generating registration data.
  • Monitor validation performance indicators and proactively address challenges to maintain continuous compliance.

The salary for this position is expected to range between $114,100 and $211,900 per year.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

Essential Requirements:

  • Bachelor's degree in Biomedical Engineering, Chemistry, Pharmacy, Chemical Engineering, or Pharmaceutical Technology.
  • Minimum 5 years' experience in manufacturing, technical development, or quality within the pharmaceutical industry.
  • Hands-on experience leading and managing validation projects.
  • Strong knowledge of manufacturing processes, process equipment, and applied statistics.
  • Proven ability to write and review technical reports and validation documentation.
  • Fluent in English and proficient in the local site language.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings


Salary Range

$114,100.00 - $211,900.00


Skills Desired

Applied Statistics, Assembly Language, Change Control, Chemical Engineering, Continual Improvement Process, Cost Reduction, Data Analytics, Electronic Components, General Hse Knowledge, Including Gdp, Knowledge Of Capa, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Manufacturing Technologies, Process and Cleaning Validation, Process Control, Process Simulation, Risk Management, Root Cause Analysis (RCA), Scientific Method, Six Sigma, Statistical Analysis, Technology Transfer

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