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Pharmaceutical Validation Jobs (NOW HIRING)

ICU Medical

Senior Validation Engineer

Austin, TX · On-site

$110 - $150/hr

Bachelor's degree from an accredited college or university * 7+ years of validation, science/technical or engineering background required, pharmaceutical validation or engineering experience ...

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Argenta

Validation Specialist

Shawnee, KS · On-site

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related field, and 2 years of experience in pharmaceutical validation, quality systems, or related GMP-regulated ...

Argenta

Validation Specialist

Shawnee, KS · On-site

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related field, and 2 years of experience in pharmaceutical validation, quality systems, or related GMP-regulated ...

Piramal Pharma Limited

QA Validation Engineer

Bethlehem, PA · On-site

$71K - $91K/yr

... pharmaceutical cGMP, industry standards, and regulations to make sound regulatory interpretation ... validation laws and legislations that are enforced from time to time Physical Demands: Physical ...

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How much do pharmaceutical validation jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for pharmaceutical validation 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 pharmaceutical validation?

A Pharmaceutical Validation job involves ensuring that systems, equipment, and processes in the pharmaceutical industry meet regulatory and quality standards. Professionals in this role develop protocols, conduct testing, and document validation activities to ensure compliance with regulations like FDA, EU GMP, and ISO standards. They work with manufacturing processes, laboratory instruments, and software to verify that products are consistently produced and controlled according to required quality standards. This role is critical in maintaining drug safety, efficacy, and regulatory approval.

What are some of the main challenges encountered in a pharmaceutical validation role?

One of the main challenges in Pharmaceutical Validation is staying updated with constantly evolving regulatory requirements and ensuring that all validation activities meet stringent compliance standards. Professionals often manage multiple concurrent projects, which requires effective prioritization, organization, and close coordination with cross-functional teams such as quality assurance, manufacturing, and engineering. Thorough documentation and meticulous attention to detail are essential, as even minor oversights can lead to compliance issues. However, overcoming these challenges provides valuable problem-solving experience and opportunities for advancement within quality assurance, regulatory affairs, or project management.

What are the key skills and qualifications needed to thrive in pharmaceutical validation, and why are they important?

To thrive in Pharmaceutical Validation, you need a strong background in pharmaceutical sciences or engineering, familiarity with regulatory guidelines (such as FDA, GMP, and ICH), and hands-on experience in validation protocols. Proficiency with validation lifecycle documentation tools, quality management systems (QMS), and specialized software like TrackWise or ValGenesis is essential. Attention to detail, analytical thinking, and excellent collaboration and communication skills are highly valued in this role. These competencies ensure that pharmaceutical processes, equipment, and systems meet strict quality standards, supporting product safety and regulatory compliance.

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Pharmaceutical Validation jobs near you
Infographic showing various Pharmaceutical Validation 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 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Senior Autoclave Validation Technician

Progressive Recovery, Inc

Dupo, IL • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 18 days ago

Key responsibilities

  • Perform autoclave qualification and validation activities, including installation, operational, and performance qualification.

  • Conduct thermal mapping studies, heat distribution, heat penetration, and sterilization cycle verification, and analyze validation data.

  • Perform scheduled preventive maintenance, inspect, clean, calibrate, and replace wear components on sterilization equipment.

Job description

Job Type
Full-time
Description
REPORTS TO: FIELD SERVICE MANAGER
We are seeking a highly motivated and detail-oriented Autoclave Validation & Preventive Maintenance Technician to support the installation, qualification, validation, preventive maintenance, calibration, troubleshooting, and repair of laboratory and production autoclaves. This position will primarily focus on Astell autoclaves but will also support sterilization equipment from other leading manufacturers in laboratory, pharmaceutical, biotechnology, healthcare, research, and industrial environments.
The ideal candidate will possess strong mechanical and electrical troubleshooting skills, experience performing thermal validation studies, and a solid understanding of sterilization processes and regulatory compliance requirements. This role requires frequent travel to customer sites and direct interaction with laboratory managers, validation teams, maintenance personnel, and quality professionals.
Key Responsibilities
Validation Services
  • Perform autoclave qualification and validation activities, including:
  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Execute thermal mapping studies using data loggers, thermocouples, and validation software
  • Conduct heat distribution, heat penetration, and sterilization cycle verification studies
  • Analyze validation data and prepare comprehensive validation reports
  • Verify cycle performance and sterilization efficacy in accordance with customer protocols and regulatory requirements
  • Support customer audits and compliance activities related to sterilization equipment

Preventive Maintenance & Service
  • Perform scheduled preventive maintenance on Astell autoclaves and other sterilization equipment
  • Inspect, clean, calibrate, and replace wear components including:
  • Door seals and gaskets
  • Solenoid valves
  • Pressure transducers
  • Ability to work independently and manage multiple service assignments
  • Valid driver's license and ability to travel regularly

Requirements
Preferred Qualifications
  • Direct experience servicing Astell autoclaves
  • Experience with autoclaves from manufacturers such as:
  • Astell Scientific
  • Tuttnauer
  • Priorclave
  • Consolidated Sterilizer Systems
  • Getinge
  • STERIS
  • Knowledge of GMP, GLP, FDA, USP, ISO, and pharmaceutical validation requirements.
  • Experience in pharmaceutical, biotechnology, healthcare, research laboratory, or regulated manufacturing environments
  • Technical degree or certification in electronics, instrumentation, mechatronics, industrial maintenance, or a related field
  • Familiarity with PLC-based control systems and industrial instrumentation
  • Experience with steam systems and utility equipment

Travel Requirements
  • Travel up to 50-75%, depending on customer demand and geographic territory
  • Ability to travel overnight for multi-day customer projects.
  • Occasional weekend work to support customer validation schedules and facility shutdowns
  • Potential for limited international travel

Desired Candidate Profile
The ideal candidate enjoys working independently in customer-facing environments and has a passion for technical problem-solving. They possess a strong understanding of sterilization
  • Temperature probes
  • Steam traps
  • Vacuum pumps
  • Safety devices
  • Water treatment components
  • Troubleshoot mechanical, electrical, pneumatic, and control system failures
  • Diagnose and repair issues involving:
  • Steam generation systems
  • Heating elements
  • PLC controls
  • HMI interfaces
  • Vacuum systems
  • Temperature and pressure control systems
  • Perform emergency service calls and corrective maintenance as required

Customer Support
  • Provide operator and maintenance training to customers
  • Serve as the primary technical contact during service visits
  • Document all service activities through detailed field service reports
  • Communicate equipment performance findings and recommend corrective actions
  • Maintain strong customer relationships through professional service delivery

Required Qualifications
  • Minimum 3-5 years of experience servicing, maintaining, validating, or calibrating autoclaves, sterilizers, laboratory equipment, or related thermal process systems
  • Experience performing thermal validation studies and using temperature mapping equipment
  • Strong understanding of sterilization principles and autoclave operation
  • Mechanical and electrical troubleshooting experience
  • Ability to read and interpret:
  • Electrical schematics
  • Wiring diagrams
  • P&IDs
  • Technical service manuals
  • Experience using diagnostic and calibration equipment
  • Strong computer skills, including report generation and data analysis
  • Excellent communication and customer service skills equipment and validation practices, are meticulous in documentation, and take pride in helping customers maintain compliance while maximizing equipment reliability and performance.

What We Offer
  • Competitive salary
  • Performance-based bonus program
  • Health, dental, and vision insurance
  • 401(k) with company match
  • Company-paid travel expenses
  • Laptop, phone, tools, and calibration equipment
  • Manufacturer and validation training programs
  • Career advancement opportunities within a growing technical service organization
  • Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

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