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Overnight Traveling Engineer Jobs in Indiana (NOW HIRING)

PinnaclePartners

Controls Engineer

Laotto, IN

$100K - $120K/yr

... travel with limited overnight travel First shift Monday-Friday schedule with minimal overtime or weekend work Long-tenured, family-owned organization with a collaborative engineering environment ...

Orion Talent

Service Engineer

Warsaw, IN · On-site

$38/hr

You will be home based or report to the office in Warsaw, Indiana for daily travel and overnight ... engineering and consulting, advanced services, extensions, upgrades and retrofits, end of life ...

Toyota

Project Engineer

Indianapolis, IN · On-site

Project Engineer Job Overview: A Project Engineer generally is new to our field with minimal or no ... Provide Customer support for ongoing and warranty projects Travel Requirements: * 30% overnight ...

Toyota

Software Project Engineer

Indianapolis, IN · On-site

The Project Engineer provides oversight and is responsible for all phases of various software ... Travel Requirements: * 50-75% overnight travel (Travel expenses paid by Toyota Automated Logistics ...

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Overnight Traveling Engineer information

What is the difference between Overnight Traveling Engineer vs Railroad Conductor?

AspectOvernight Traveling EngineerRailroad Conductor
Required CredentialsEngineer certification, locomotive operation licenseConductor certification, safety training
Work EnvironmentLocomotive cab, traveling overnight, on tracksTrain cars, station platforms, on-site at stations
Employer & IndustryRailroads, freight and passenger servicesRailroads, passenger and freight services
Common Search/ComparisonYesYes

The Overnight Traveling Engineer primarily operates trains overnight, focusing on locomotive control and safety. In contrast, the Railroad Conductor manages train operations, passenger safety, and crew coordination. Both roles are essential in rail transportation, but they differ in responsibilities and certifications. Understanding these differences helps job seekers find the right career path in the rail industry.

What are popular job titles related to Overnight Traveling Engineer jobs in Indiana? For Overnight Traveling Engineer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Overnight Traveling Engineer jobs in Indiana look for? The top searched job categories for Overnight Traveling Engineer jobs in Indiana are:
What cities in Indiana are hiring for Overnight Traveling Engineer jobs? Cities in Indiana with the most Overnight Traveling Engineer job openings:
Overnight Traveling Engineer jobs near you
Infographic showing various Overnight Traveling Engineer job openings in Indiana as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution.

Validation Engineer

Sterling Engineering Inc.

Indianapolis, IN • On-site

$75K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago

Job description

Title: Validation Engineer - VHP / Aseptic Processing / Pharmaceutical Manufacturing
Location: Indianapolis, IN or remote in Northeast US
Hire Type: Direct Hire
Compensation: $75,000 - $120,000
Benefits: Health, Dental, Vision, 401K, PTO
Must have Skill Set:

  • Must have proven Validation Engineering experience in a pharmaceutical, biotech, life sciences, or regulated manufacturing environment.
  • Must have equipment validation experience. Cleanroom validation experience is also acceptable.
  • Must have proven experience developing and executing decontamination cycle development and validation activities.
  • Must have hands-on experience with Vaporized Hydrogen Peroxide (VHP/VPHP) systems.
  • Must have experience with Steris VHP generators or similar VHP generator systems.
  • Must have experience working in aseptic processing environments, including sterilization of equipment prior to production.
  • Must have strong pharmaceutical validation documentation experience, including validation protocols, IQ, OQ, PQ documentation, validation reports, and GMP documentation.
  • Must be willing and able to travel up to 60% to customer sites, including local day trips and overnight travel throughout the Northeastern United States.

Overview:

We are seeking an experienced Validation Engineer to support pharmaceutical, biotech, and advanced therapy manufacturing projects. This is a highly hands-on customer-facing role responsible for equipment validation, commissioning, qualification, and decontamination cycle development for aseptic manufacturing systems.

The ideal candidate will have proven experience in Validation Engineering, equipment validation, VHP (Vaporized Hydrogen Peroxide) systems, VHP cycle development, and aseptic processing environments. This individual will work closely with engineering teams and customers to execute Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities while ensuring compliance with pharmaceutical quality and regulatory requirements.

This position requires regular travel to customer sites. Candidates must be comfortable traveling up to 60%, including both local day trips and overnight travel throughout the Northeast region.

Job Duties:

  • Lead and support validation engineering activities for pharmaceutical and biotechnology manufacturing equipment.
  • Execute and support equipment validation, including FAT, SAT, IQ, OQ, and PQ activities.
  • Develop, optimize, and validate Vaporized Hydrogen Peroxide (VHP/VPHP) decontamination cycles.
  • Perform cycle development and support Performance Qualification activities related to VHP sterilization processes.
  • Work directly with customers and field service teams during equipment installation, commissioning, startup, and qualification.
  • Support validation activities within aseptic processing environments, ensuring proper sterilization of manufacturing equipment prior to production.
  • Prepare, review, and execute pharmaceutical validation documentation, including validation protocols, reports, SOPs, deviations, and change control documentation.
  • Ensure compliance with GMP, regulatory, customer, and internal quality requirements.
  • Support quality investigations, process improvements, inspections, and corrective actions.
  • Collaborate with engineering, quality, manufacturing, and customer teams throughout project execution.
  • Travel to customer facilities for validation, commissioning, startup, and qualification activities (approximately 60% travel).

Qualifications:

  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline, or equivalent industry experience.
  • Proven experience in Validation Engineering is required.
  • Proven experience with equipment validation is required.
  • Experience with cleanroom validation is acceptable in lieu of equipment validation experience.
  • Proven experience with Vaporized Hydrogen Peroxide (VHP/VPHP) systems is required.
  • Experience with Steris VHP generators is strongly preferred.
  • Proven experience developing decontamination cycles and VHP cycle development is required.
  • Experience working in aseptic processing and sterile pharmaceutical manufacturing environments is required.
  • Strong knowledge of pharmaceutical validation principles, GMP requirements, and regulated manufacturing environments.
  • Experience preparing and executing pharmaceutical documentation, including IQ/OQ/PQ protocols, validation reports, SOPs, and related quality documentation.
  • Excellent communication, problem-solving, and organizational skills.
  • Proficiency with Microsoft Office.
  • Ability and willingness to travel up to 60%, including local day travel and overnight travel throughout the Northeastern United States.


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.