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Contract Method Validation Jobs in Marion, NC (NOW HIRING)

RS&H

Assistant Resident Engineer

Arden, NC · On-site

$94K - $120K/yr

... methods, and procedures of a professional work environment. Qualifications: * 4+ years' experience ... Experience working with contractors to resolve issues dealing with contract conformance ...

RS&H

Assistant Resident Engineer

Arden, NC

$94K - $120K/yr

... methods, and procedures of a professional work environment. Qualifications: * 4+ years' experience ... Experience working with contractors to resolve issues dealing with contract conformance ...

RS&H

Assistant Resident Engineer

Arden, NC · On-site

$94K - $120K/yr

... methods, and procedures of a professional work environment. Qualifications: * 4+ years' experience ... Experience working with contractors to resolve issues dealing with contract conformance ...

M Force

Manufacturing Engineer I

Valdese, NC · On-site

$80K - $85K/yr

... methods, tooling, and fixture design Experience with process improvement and manufacturing ... and process validation Job presented by M Force Partners M Force Partners is a specialized ...

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All JobsContract Method Validation JobsContract Method Validation Jobs in Marion, NC

Contract Method Validation information

See Marion, NC salary details

$20

$48

$72

How much do contract method validation jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for contract method validation in Marion, NC is $48.24, according to ZipRecruiter salary data. Most workers in this role earn between $36.59 and $58.65 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.

Contract Method Validation jobs near you

Validation Specialist

Accord Technologies Inc.

Marion, NC • On-site

Contractor

Re-posted 8 days ago

Job description

Validation Specialist
Marion, NC, USA
12 months
W2 contract
 
 
Must have experience supporting medical device manufacturing under ISO 13485 Writing test protocols within KNEAT Gx Knowledge of CQV (Commissioning Qualification and Validation) process
 
 
Required Qualifications: 
• The Validation Specialist (Contract) will support pharmaceutical and medical device operations by executing and maintaining compliant validation activities using Kneat Gx as the electronic validation lifecycle management system
This role is focused on hands on execution of validation deliverables to support equipment, process, utility, and computerized system readiness in accordance with FDA, ISO, and cGMP requirements
• The specialist will work closely with Engineering, Quality, Automation, IT, and Operations to ensure systems and equipment are validated, audit ready, and capable of supporting safe, compliant production
• Validation Execution (Primary Role)
• Execute IQ, OQ, PQ, requalification, and validation maintenance activities for pharma and medical device manufacturing systems.
• Manufacturing and packaging equipment
• Utilities (compressed air, clean utilities, environmental controls)
• Computerized systems (automation, data acquisition, MES, LIMS, vision systems)
• Apply risk-based validation methodologies aligned with GAMP 5 and industry best practices.
Preferred Qualifications:
• Experience supporting medical device manufacturing under ISO 13485.
• Experience with automation and controls (PLC/SCADA), vision systems, or MES.
• Experience supporting high speed packaging or assembly lines.
• Exposure to validation remediation or regulatory commitment work
Required Technical Skills:
• KNEAT Gx Lifecycle Management
• Author, execute, review, and route validation documents within KNEAT Gx.
• Maintain end to end traceability between:
• User Requirements (URS)
• Risk Assessments
• Test cases and protocols
• Deviations and final reports
• Ensure proper use of KNEAT Gx workflows, execution controls, and electronic approvals.
• Maintain compliance with 21 CFR Part 11 and data integrity expectations.
• Deviation, Change Control & CAPA Support
• Document and investigate validation deviations within KNEAT Gx
• Support change control impact assessments affecting validated systems
• Participate in root cause analysis and CAPA implementation when required
Regulatory & Quality Compliance
• Ensure validation deliverables comply with:
• oFDA cGMP regulations (21 CFR Parts 210/211, Part 11)
• ISO 13485 (Medical Devices)
• Internal Quality Management System (QMS) requirements
• Support regulatory inspections and customer audits by providing validation documentation and responses.
• Maintain validation documentation in a state of continuous inspection readiness
Responsibilities:
• Collaborate with Engineering, Quality, IT, Automation, Manufacturing, and external vendors.
• Provide on floor support during commissioning, troubleshooting, and validation execution.
• Support site initiatives such as new equipment introduction, line upgrades, remediation efforts, and capacity expansions.
• Detail oriented with a strong compliance mindset
• Ability to work independently under contract deliverables
• Strong problem solving and root cause analysis skills
• Effective communication with cross functional teams
• Comfortable working in production and controlled environments
• On site support in a controlled GMP manufacturing environment
• May require off shift or weekend support during execution windows
• PPE and gowning requirements may apply depending on area
Additional Details:
• Industry: Pharmaceutical & Medical Devices
• Contract Type: Contract (On site / Hybrid, as required)
• Duration: Contract basis (length defined by project needs)
• On site support in a controlled GMP manufacturing environment
• May require off shift or weekend support during execution windows
• PPE and gowning requirements may apply depending on area