ZipRecruiter

Log In

1

Validation Engineer H1B Jobs (NOW HIRING)

BMR Infotek

Lead Database Engineer

Charlotte, NC · On-site

$45 - $55/hr

Visa- H1B/USC **Location:** Charlotte, NC / Iselin, NJ (Hybrid) **Rate:** $45-$55/hr on W2 **Client ... Migration Preparation** - Execute pre-migration checks, validate target environments, schedule ...

Pharma Bioserv

Be Seen First

Process Engineer

Wilson, NC · On-site

Supporting New Product Introduction/ process validation in Downstream manufacturing facility ... We do not provide H1B Visa support / No C2C available. Company Description Pharma-Bio Serv, a ...

Trialon Corporation

Optical Engineer

Auburn Hills, MI · On-site

$122K - $158K/yr

Bachelor's degree in Engineering (in optics/physics) or Engineering/Mathematics background or ... No Corp to Corp. NO H1B Visa sponsorship. Must be US Citizen or have valid US Green Card.

Trialon Corporation

Optical Engineer

Auburn Hills, MI · On-site

$122K - $158K/yr

Bachelor's degree in Engineering (in optics/physics) or Engineering/Mathematics background or ... No Corp to Corp. NO H1B Visa sponsorship. Must be US Citizen or have valid US Green Card.

FHR

MO-1231-Cloud Infrastructure Engineer (759097)

Newark, NJ · On-site

$112K - $147K/yr

... will validate all previous experiences for all projects as well as work documents (h1B, EAD, GC ... Newark, NJ 07102 Our direct client has an opening for Cloud Infrastructure Engineer (759097) This ...

Jones Edmunds

Engineer - Civil Engineering

Tampa, FL · On-site

Valid driver's license with acceptable MVR. Why Join Jones Edmunds? * Comprehensive Benefits ... H1B, etc.,) to fill this position. As a condition of employment with Jones Edmunds & Associates any ...

previous pagenext page

Showing results 21-40

All JobsValidation Engineer H1B Jobs

Validation Engineer H1B information

See salary details

$22

$51

$78

How much do validation engineer h1b jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for validation engineer h1b in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is a validation engineer H1B?

Validation Engineers on H1B visas are professionals from abroad who are employed in the United States to ensure that systems, equipment, and processes meet regulatory and quality standards. They typically work in industries such as pharmaceuticals, biotechnology, and manufacturing, performing testing, documentation, and analysis to verify product compliance. The H1B visa allows U.S. employers to temporarily employ foreign workers in specialty occupations that require theoretical or technical expertise, such as validation engineering. These roles often require a bachelor’s degree or higher in engineering or a related field.

What are the key skills and qualifications needed to thrive as a validation engineer?

To thrive as a Validation Engineer, you need a strong background in engineering principles, quality assurance, and regulatory compliance, typically supported by a degree in engineering or a related field. Familiarity with validation tools, statistical analysis software, and knowledge of industry standards such as FDA regulations or ISO guidelines are essential. Strong attention to detail, critical thinking, and effective communication skills help distinguish top performers in this role. These skills are crucial for ensuring products and processes meet rigorous quality and safety standards, reducing risks and maintaining regulatory compliance.

What are some common challenges validation engineers face when working in regulated industries, and how can they prepare for them?

Validation Engineers, especially those in regulated industries like pharmaceuticals or medical devices, often encounter challenges such as evolving regulatory requirements, tight project timelines, and the need for meticulous documentation. To prepare, it's essential to stay updated on industry standards (such as FDA or ISO guidelines), develop strong organizational skills for thorough record-keeping, and collaborate closely with cross-functional teams, including quality assurance and production. Proactively communicating and participating in ongoing training can also help mitigate compliance risks and ensure successful project outcomes.

What is the difference between Validation Engineer H1B vs Quality Assurance Engineer?

AspectValidation Engineer H1BQuality Assurance Engineer
Required CredentialsBachelor's in Engineering or related field, certifications like CSQE or CQE beneficialBachelor's in Engineering, Computer Science, or related field, certifications like CQE or CQA helpful
Work EnvironmentManufacturing, pharmaceutical, or biotech industries focusing on product validationSoftware, manufacturing, or service industries focusing on process and product quality
Employer & Industry UsageCommon in regulated industries requiring validation processesWidespread across industries emphasizing quality standards

Validation Engineers H1B primarily focus on validating products and processes in regulated industries, often requiring specific certifications. Quality Assurance Engineers also ensure product quality but have a broader scope, including process audits and software testing. Both roles share similar credentials but differ in industry focus and specific responsibilities.

More about Validation Engineer H1B jobs

What cities are hiring for Validation Engineer H1B jobs?

Cities with the most Validation Engineer H1B job openings:

What states have the most Validation Engineer H1B jobs?

States with the most job openings for Validation Engineer H1B jobs include:

What job categories do people searching Validation Engineer H1B jobs look for?

The top searched job categories for Validation Engineer H1B jobs are:

Validation Engineer H1B jobs near you
Infographic showing various Validation Engineer H1B job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 3% Part Time, and 4% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Sr. Manager Equipment Maintenance - Pharma Sterile Fill

MRINetwork Jobs

Spokane, WA • On-site

$125K - $180K/yr

Full-time

Medical, Dental, Retirement, PTO

Re-posted 29 days ago

Job description

Our client – a global and growing BioPharma CDMO company needs an Sr. Manager – Equipment Maintenance with Pharmaceutical Industry experience at their expanding plant in WA state, Excellent total comp. up to $205K+ with excellent Benefits (starting day 1) + Generous Relocation Bonus. If needed client will support H1B visa transfer.

Job Posting # 2713   

 

Job Title:  Sr. Manager Equipment Maintenance – Pharma Sterile Fill

Location:  Spokane, WA                                                                 

Relocation: The client offers a generous lumpsum bonus for relo assistance.

Compensation: Salary range $125K - $180K + Annual Bonus (15%)

Full Benefits - right away: Medical, Dental, 15 days’ vacation/Sick time, Holidays, 401k (match up to 4%).

Company Info:

Our client is a growing CDMO company in the Pharmaceutical Industry. They are a part of a global parent company with sites in many countries. This is an integrated contract development and manufacturing organization (CDMO) offering specialized Aseptic Sterile manufacturing, filling and lyophilization of drug products in Vials. They have around 1,300 people at this manufacturing site in Spokane, WA

Group Info: Lead the Equipment Maintenance group supporting the existing and expansion site in Spokane, WA. The group has 4 supervisors for weekday and weekend working 24*7 in 12 hr shifts with a round 20 maintenance Technicians under the 4 supervisors. This role will report to the Assoc. Director of Maintenance, who will then report to the Sr. Director of Engineering and Maintenance who is over a group of around 80 technical staff.

Note1: The company recently completed their 3rd state-of-the-art Sterile Liquid compounding & Vial Filling line and are currently expanding again with a 4th line at this site.

Note 2: This is a hands-on role and the manager is expected to lead the team by example and perform some strategic Maintenance Engineering work and also lead this group.

 

Note 3: This group supports only the equipment maintenance for the plant. They have separate groups for Facility/Utility Management, Reliability and Engineering.

 

Note 4: Client will support transfer of existing TN1 or H1B Visa for this permanent direct hire role, but will not sponsor for a new H1B visa.

Summary:

  • The Senior Manager, Equipment Maintenance is responsible for the day-to-day leadership and execution of GMP equipment maintenance, reliability, and lifecycle management activities supporting pharmaceutical manufacturing operations. 
  • This role ensures equipment uptime, regulatory compliance, and inspection readiness through effective maintenance strategies, strong people leadership, and cross-functional collaboration. 
  • The Senior Manager translates site maintenance strategy into tactical plans and execution, leads maintenance teams and supervisors, and partners closely with Manufacturing, Quality, Validation, and Engineering to maintain a safe, compliant, and efficient operating environment.

Job Description:

 

Equipment Maintenance & Reliability Execution

  • Lead execution of preventive, predictive, and corrective maintenance programs for GMP manufacturing equipment, utilities, and critical systems.
  • Ensure maintenance activities are compliant, effective, and completed on schedule.
  • Monitor equipment performance, reliability metrics, and asset health; drive continuous improvement initiatives.
  • Act as escalation support for complex equipment issues impacting safety, quality, or production.
  • Support asset lifecycle activities, including reliability improvements and obsolescence mitigation.

People Leadership & Supervision

  • Lead, coach, and develop maintenance managers, supervisors, engineers, and technical staff.
  • Set clear performance expectations, objectives, and development plans for direct reports.
  • Foster a strong safety culture emphasizing accountability, compliance, and continuous improvement.
  • Support workforce planning and day-to-day resource allocation to meet production needs.

Regulatory Compliance & Inspection Readiness

  • Ensure maintenance activities comply with cGMP, FDA, and global regulatory requirements.
  • Lead or support equipment-related deviation investigations, root cause analyses, and CAPA execution.
  • Maintain inspection-ready documentation including maintenance records, SOPs, and reports.
  • Participate in regulatory, client, and internal audits; support audit readiness activities.

Cross-Functional Collaboration

  • Partner with Manufacturing, Quality, Validation, Engineering, EHS, and Supply Chain to support operational objectives.
  • Provide technical input to equipment upgrades, process improvements, and capital projects.
  • Collaborate with Validation and Engineering on equipment qualification (IQ/OQ/PQ), changes, and commissioning activities.

Budget & Vendor Oversight

  • Support management of maintenance operating expenses, contracts, and service agreements.
  • Oversee vendors and contractors to ensure safe, compliant, and cost-effective execution of work.
  • Contribute to maintenance planning, forecasting, and continuous cost improvement efforts.

Candidate Must Have:

  • Bachelor’s degree in Engineering (Mechanical, Electrical, Industrial, Chemical, or related discipline)
  • 8+ years of maintenance experience in industrial manufacturing
  • 5+ years of experience in pharmaceutical or biopharmaceutical manufacturing
  • 3+ years of leadership experience managing maintenance teams or supervisors
  • GMP equipment maintenance and reliability programs
  • Deviation investigations and CAPA execution
  • Inspection readiness and audit participation
  • Vendor and contractor oversight
  • Strong knowledge of GMP equipment maintenance, reliability engineering, and asset management
  • Understanding of FDA and global regulatory requirements
  • Ability to interpret technical documentation, SOPs, and engineering drawings
  • Experience with maintenance management systems (CMMS)

Candidate Nice to Have:

  • Certified Maintenance and Reliability Professional. (CMRP).
  • Lean, Six Sigma, or continuous improvement training
  • Project management experience
  • Pharmaceutical engineering or ISPE/PDA training
  • Advanced degree in Engineering or MBA
  • Automation experience using Rockwell PLC/HMI/SCADA systems
  • Experience working in a fast-paced Pharma Contract Manufacturing Organization (CDMO)

Keywords: Maintenance, reliability, Pharma, CDMO, manufacturing, plant, FDA, GMP, Sterile Aseptic liquid filling, Isolators, Clean rooms, Lyophilization, contract Manufacturing, Manager, CMRP, PLC, Automation.