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Contract Method Validation Jobs in Randolph, NJ (NOW HIRING)

ADP, Inc.

Sr. Scientist - QC Microbiology

Branchburg, NJ · On-site

$87 - $147/hr

Looking ahead, we also anticipate expanding into the global contract manufacturing organization ... They may also lead commercialization and technical agenda projects such as method validations ...

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Socket.dev

Sr. Scientist - QC Microbiology

Branchburg, NJ · On-site

$87 - $147/hr

Looking ahead, we also anticipate expanding into the global contract manufacturing organization ... They may also lead commercialization and technical agenda projects such as method validations ...

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All JobsContract Method Validation JobsContract Method Validation Jobs in Randolph, NJ

Contract Method Validation information

See Randolph, NJ salary details

$23

$53

$80

How much do contract method validation jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for contract method validation in Randolph, NJ is $53.44, according to ZipRecruiter salary data. Most workers in this role earn between $40.53 and $65.00 per hour, depending on experience, location, and employer.

What is the difference between Contract Method Validation vs Analytical Method Validation?

AspectContract Method ValidationAnalytical Method Validation
PurposeValidates that a contracted method meets specific requirements for a particular project or clientEnsures an analytical method is accurate, reliable, and reproducible for testing purposes
ScopeTypically project-specific, focusing on methods used under contractual agreementsBroader, covering method development, validation, and routine testing
CredentialsOften requires validation expertise, GMP knowledge, and industry-specific certificationsRequires analytical chemistry knowledge, validation experience, and relevant certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing settings with client-specific projectsLaboratories performing routine testing and method development in similar industries

Contract Method Validation focuses on validating methods for specific client projects, while Analytical Method Validation ensures the overall reliability of testing methods used routinely in laboratories. Both roles require similar credentials and work in related environments, but their scope and purpose differ.

What cities near Randolph, NJ are hiring for Contract Method Validation jobs?

Cities near Randolph, NJ with the most Contract Method Validation job openings:

Contract Method Validation jobs near you

Software Test Method Validation (TMV)

Katalyst CRO

South Plainfield, NJ • On-site

Full-time

Re-posted 27 days ago

Job description

Job Summary:
Katalyst CRO is a company focused on software and systems verification for FDA-regulated medical devices. They are seeking a Software Test Method Validation (TMV) engineer to develop and maintain verification protocols, perform various levels of testing, and ensure compliance with industry regulations.
Responsibilities:
• Develop, execute, and maintain software/system verification protocols and test strategies for FDA-regulated medical devices.
• Perform functional, integration, regression, and system-level testing for embedded software and firmware applications.
• Validate safety-critical workflows including alarms, dosage calculations, thermal control systems, and patient safety features.
• Execute risk-based testing aligned with FMEA and ISO 14971 requirements.
• Design and maintain automated GUI and regression frameworks using Squish, Selenium, Python, and Pytest.
• Integrate automated test suites with Jenkins/GitLab CI pipelines for continuous validation and release readiness.
• Improve test coverage, execution efficiency, and defect detection rates through automation initiatives.
• Perform Hardware-in-the-Loop (HIL) testing using LabVIEW, TCUs, and embedded communication interfaces.
• Validate embedded communication protocols including TCP/IP, Ethernet, UART, and serial communication.
• Use oscilloscopes, multimeters, flow meters, and J-Link debuggers for hardware/software integration testing.
• Create and maintain test cases, protocols, traceability matrices (RTM), verification reports, and defect documentation.
• Ensure compliance with IEC 62304, ISO 13485, IEC 60601/61010, IEC 62366, FDA 21 CFR Part 11, and QMS standards.
• Support FDA audits, 510(k) submissions, CAPA investigations, and post-market remediation activities.
• Participate in Agile/Scrum ceremonies and cross-functional collaboration with firmware, hardware, systems, and QA teams.
• Lead defect triage, root-cause analysis, and corrective/preventive action verification.
• Support change control and release validation activities for medical device software products.
Qualifications:
Required:
• Software V&V for medical devices and embedded systems
• Test Automation: Squish, Selenium, Python, Pytest
• CI/CD Tools: Jenkins, GitLab CI, Azure DevOps, Bitbucket
• ALM & Traceability Tools: Jama Connect, IBM DOORS, Polarion ALM, Helix ALM
• Embedded interfaces: UART, TCP/IP, Ethernet, serial communication
• HIL testing, LabVIEW, J-Link debugger
• SQL, HTML, CSS
Company:
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is headquartered in South Plainfield, USA, with a team of 51-200 employees. The company is currently Growth Stage.

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