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Instron Jobs (NOW HIRING)

Illinois Tool Works Inc

NC Machinist

Binghamton, NY

$29.30/hr

Company Description Instron is a global organization that designs, manufactures, sells and services mechanical testing systems. Have you ever wondered how a potato chip always has the right ...

Boydcorp

Senior Quality Technician

Grand Rapids, MI

Use inspection and test equipment including Keyence systems, Instron equipment, microscopes, calipers, gauges, and other approved measurement tools to verify product conformance. Monitor product ...

Illinois Tool Works Inc

NC Machinist

Binghamton, NY · On-site

$21.70 - $29.30/hr

Company Description Instron is a global organization that designs, manufactures, sells and services mechanical testing systems. Have you ever wondered how a potato chip always has the right ...

Apex Informatics

Reliability Tester

Mountain View, CA · On-site

$40 - $45/hr

... Instron, strain gauge, accelerometer, etc. Preferred qualifications: Desired BA/BS or higher degree in Mechanical Engineering, Electrical Engineering, Material Science, Physics or related fields.

Certified Employment Group

Be Seen First

Medical Device Assembler - NOT REMOTE

Santa Rosa, CA · On-site

$21 - $26/hr

Microscope | CMM | Instron | Calipers | Micrometers | Pin Gauges | Snap Gauges WHY JOIN US? ⭐ 4-day work week (3-day weekends!) ⭐ Competitive pay ⭐ Growing medical device industry ⭐ Team ...

SigSauer

R&D Engineering Technician III

Exeter, NH

Instron Machine; Instron Programming; Keyence System; Garmin; Recoil; High Speed Video; High Speed Cameras; Toxic Fume Chambers; Sound; Flash and other small arms test apparatus as directed by the ...

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Instron information

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$60K

$105.7K

$156K

How much do instron jobs pay per year?

As of Jun 25, 2026, the average yearly pay for instron in the United States is $105,714.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What does the Instron do?

An Instron is a testing technician or engineer who operates Instron machines to perform material and product testing, such as tensile, compression, and fatigue tests. They set up equipment, interpret test data, and ensure tests meet industry standards, often requiring knowledge of materials science and calibration skills.

What is an Instron operator and what do they do?

An Instron operator is a professional who operates and maintains Instron testing machines, which are commonly used for materials testing such as tensile, compression, and flexural tests. These machines are essential in quality control and research labs to determine the mechanical properties of materials like metals, plastics, and composites. The operator is responsible for preparing specimens, setting up tests, running the equipment, and accurately recording and analyzing data. They also perform regular maintenance and ensure compliance with safety standards.

What are some common challenges faced by technicians working with Instron testing machines, and how can they be addressed?

Technicians working with Instron testing machines often encounter challenges such as ensuring precise calibration, troubleshooting software or hardware issues, and maintaining consistent test results across different materials. Addressing these challenges typically involves staying up to date with manufacturer training, following strict quality control protocols, and collaborating closely with engineering and quality assurance teams. Regular preventive maintenance and clear documentation of test procedures also help minimize errors and downtime, ensuring reliable results and smooth workflow.

What kind of training is required to use Instron?

Instron operators typically require training on the specific testing equipment, including understanding machine operation, safety procedures, and data interpretation. Training may be provided by the employer or through manufacturer-led courses, and familiarity with materials testing standards is often beneficial.

What is the difference between Instron vs Material Testing Technician?

AspectInstronMaterial Testing Technician
Required CredentialsEngineering degree or technical certification, training in testing equipmentHigh school diploma or associate degree, technical training in material testing
Work EnvironmentManufacturing labs, research facilities, testing centersMaterial labs, manufacturing plants, quality control departments
Industry UsageUsed across engineering, aerospace, automotive, and research sectorsCommon in manufacturing, quality assurance, and materials science industries

Instron professionals typically focus on operating advanced testing machines and analyzing material properties, often requiring specialized engineering knowledge. Material Testing Technicians perform hands-on testing and data collection on materials, usually with technical training. Both roles are vital in quality control and research, but Instron roles tend to involve more technical expertise with sophisticated equipment.

What are the key skills and qualifications needed to thrive as an Instron Operator, and why are they important?

To excel as an Instron Operator, you typically need a background in materials testing or engineering, attention to detail, and a solid understanding of mechanical properties. Familiarity with Instron testing machines, data analysis software, and safety protocols is essential, often supported by relevant technical training or certifications. Strong problem-solving skills, communication, and the ability to work independently help operators efficiently interpret results and report findings. These competencies ensure accurate testing, reliable data, and safe operation in quality control and research environments.

Is Instron a good company to work for?

Instron is a well-known manufacturer of testing equipment, and employment there typically involves roles related to engineering, manufacturing, and technical support. The company is generally considered stable with a focus on innovation and quality, which can provide a positive work environment for employees with relevant skills. However, individual experiences may vary based on specific roles and locations.

What is the cost of Instron UTM?

The cost of an Instron Universal Testing Machine (UTM) varies depending on the model, specifications, and features, typically ranging from $20,000 to over $100,000. Prices can also be influenced by optional accessories, software, and calibration services. Buyers often request quotes from authorized distributors or directly from Instron for precise pricing based on their testing needs.
More about Instron jobs
What cities are hiring for Instron jobs? Cities with the most Instron job openings:
What states have the most Instron jobs? States with the most job openings for Instron jobs include:
What job categories do people searching Instron jobs look for? The top searched job categories for Instron jobs are:
Instron jobs near you
Infographic showing various Instron job openings in the United States as of June 2026, with employment types broken down into 78% Full Time, 2% Part Time, 14% Contract, and 6% Nights. Highlights an 98% In-person, and 2% Hybrid job distribution, with an average salary of $105,714 per year, or $50.8 per hour.
Engineer, Drug Product - Prefilled Syringes (JP13400)

Engineer, Drug Product - Prefilled Syringes (JP13400)

3 Key Consulting

Thousand Oaks, CA

$36 - $41/hr

Other

Posted 11 days ago

Job description

Job Title:Engineer, Drug Product - Prefilled Syringes (JP13400)
Location:Thousand Oaks, Ca.
Business Unit:PFS And Lyo Kit Platforms
Employment Type: Contract
Duration:12 months with likely extensions or conversion to perm
Rate: $36-41/hours W2 with benefits
Posting Date:11/20/2024
Target Start Date:01/06/2025
3 Key Consulting is hiring! We are recruiting anEngineerfor a consulting engagement with our direct client, a leading global biotechnology company.
Ideal Candidate: has hands-on experience in engineering environments, particularly with tools like Instron systems and optical measurement methods, as well as proficiency in technical documentation and teamwork. They should have experience in regulated industries, preferably biopharma, biomedical, or medical devices, though aerospace or mechanical disciplines are acceptable. Proficiency in Microsoft Office is required, and CAD/SolidWorks skills are a plus. Entry-level candidates with practical experience, such as internships, are preferred, while overqualification (e.g., PhD or advanced degrees with extensive experience) is less desirable. Packaging engineering knowledge is a bonus but not mandatory.
Job Description:.
The Device Engineer will participate in the design, development, and lifecycle management design control activities for commercialized drug delivery devices. This role includes technical operations support for combination product development to global launch, clinical and commercial manufacturing, failure investigation, design change evaluation, development and execution of test procedures, and continuous improvement initiatives.
Scope includes mechanical delivery devices, such as; Prefilled syringes. The qualified candidate will be part of a sustaining device engineering team that ensures design history files of these mechanical delivery devices are maintained. The engineer will participate in cross functional teams, leading device design activities such as the development of product enhancements, analytical failure analysis and implementation of design solutions, assessment of proposed changes, support product launches, defend inspection and ensure the follow through of commitments.
Essential skills and Responsibilities:
  • Adheres to strict documentation practices in a GMP regulated environment
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Maintains combination product design history files for assigned products
  • Develops characterization test methods through fixture prototyping, reference sample creation, and GR&R analysis
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
  • Individual contributor with Leadership attributes to effectively represent device engineer within a large network/matrix organization
  • At a minimum familiar with the following standards and regulations:
  • Quality System Regulation - 21CFR820
  • Risk Management - ISO 14971
  • EU Medical Device requirements - Council Directive 93/42/EEC

Preferred Qualifications:
  • Bachelor's Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Minimum 2 year of scientific or engineering experience in a GMP regulated environment
  • Statistical Analysis software (Minitab or JMP)
  • Strong technical writing skills
  • CAD fixturing software (SolidWorks)
  • Instron force tester using BlueHill Universal
  • Experience with design controls; including (but not limited to) verification and design transfer
  • Understanding of risk assessments including hazard and probability analysis
  • Background in medical device development, commercialization and knowledge of manufacturing processes (fill-finish)
  • Ability to work independently and dynamically across functional teams
  • Excellent written and verbal communication skills
  • Ability to support complex workstreams under demanding timelines

Top Must Have Skill Sets:
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.

Day to Day Responsibilities:
  • The device engineer will support a senior engineer on a variety of projects related to laboratory testing, life cycle management, and product-based initiatives regarding prefilled syringes in both the commercial and developmental space.
  • The engineer will be expected to author protocols, reports, and further technical documentation while adhering to GMP standards.
  • Laboratory testing will primarily include the use of an Instron force tester and vision systems.
  • The identified candidate must be able to lift up to 50 lbs for receipt and transferring of material.
  • Fill-Finish experience is a bonus but not mandatory.
  • Engineer will be evaluated on ability to complete a wide variety of supporting tasks for projects in a timely manner while maintaining a high standard of quality.

Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience

Red Flags:
  • Lack of hands-on experience in engineering or a translatable field like farming or factory work.
  • Poor communication or teamwork skills, especially for candidates with no collaborative experience.
  • Unwillingness to relocate or commute daily to ATO for this on-site role.
  • Weak technical writing skills.
  • Reliance solely on theoretical or textbook knowledge without practical application.
  • No experience in relevant industries, such as medical device manufacturing, biopharma, or packaging.
  • PhDs or Masters candidates that have over 3 Years of experience

Interview Process:
Screening and then move to 1:3 team members.
We invite qualified candidates to sendyour resume torecruiting@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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