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Contract Method Validation Jobs in Scranton, PA (NOW HIRING)

Robert Half

Cost/Pricing Analyst

Olyphant, PA · On-site

We are looking for a Cost/Pricing Analyst to support proposal development, contract pricing, and ... methodologies used in submissions. * Conduct cost and price reviews for budgeting activities as ...

Wipro Limited

Structural Test Engineer

Dallas, PA · On-site

$45K - $121K/yr

This role will partner closely with contract manufacturers and fixture vendors to validate, release ... The ideal candidate brings strong technical depth in structural test methods, hands-on debug ...

GHD

Design Manager

Scranton, PA · On-site

Design engineering solutions and the associated validation process to enable the realization of a ... Contract Management: Deliver required outcomes by managing day-to-day relationships with contract ...

GHD Group

Design Manager

Scranton, PA · On-site

Design engineering solutions and the associated validation process to enable the realization of a ... Contract Management: Deliver required outcomes by managing day-to-day relationships with contract ...

Pride Mobility

Design Engineer II - Quantum

Duryea, PA · On-site

$71K/yr

... validation testing, and work cooperatively with other departments which perform inspections and ... international contract manufacturers as needed for product launches • Ensure all safety and ...

ERM

Inspector (Field Based)

Scranton, PA · On-site

The role of an Inspector working within this program requires the use of multiple methods to ... Distributing water sampling test kits and contracts to landowners, as needed. * Documenting service ...

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All JobsContract Method Validation JobsContract Method Validation Jobs in Scranton, PA

Contract Method Validation information

See Scranton, PA salary details

$22

$51

$77

How much do contract method validation jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for contract method validation in Scranton, PA is $51.47, according to ZipRecruiter salary data. Most workers in this role earn between $39.04 and $62.60 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 Scranton, PA are hiring for Contract Method Validation jobs?

Cities near Scranton, PA with the most Contract Method Validation job openings:

Contract Method Validation jobs near you

GLP Quality Assurance Manager, Contract Research Organization

RPM ReSearch

Scranton, PA • Remote

Full-time

Re-posted 2 days ago

Job description

Job Title: Quality Assurance Manager GLP


About the Role: The Quality Assurance Manager is responsible for managing daily QA activities and leading a small team of QA Associates. Reporting remotely to the QA Director, this role involves ensuring comprehensive audits of nonclinical and laboratory studies to verify compliance with protocols, Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP) (21 CFR Part 58 and Part 11), and applicable regulatory requirements. The QA Manager will also provide leadership, mentorship, and guidance to team members, driving quality assurance best practices within the facility.


Key Responsibilities:


  • Oversee and manage QA operations, ensuring thorough audits across various disciplines including non-clinical GLP studies, method validations, vendor qualifications, and equipment/software validations.
  • Act as the primary onsite QA leader, addressing day-to-day operational issues and compliance questions in the absence of the remote QA Director.
  • Conduct and oversee in-life, process, data, and facility audits to verify adherence to regulatory standards.
  • Lead audits and supervise QA investigations, ensuring robust documentation and timely resolution.
  • Maintain accurate, organized audit records and computerized documentation systems to effectively support audit activities and regulatory inspections.
  • Identify and communicate quality and compliance trends, proactively recommending and implementing process improvements.
  • Provide expert guidance and interpretations of GLP regulations, supporting the development and execution of corrective actions and SOP enhancements.
  • Serve as the primary point of contact during external client and regulatory audits, effectively representing the QA department.
  • Participate in project planning, risk assessments, and strategic implementation activities.
  • Develop and deliver GLP compliance training to facility staff, ensuring alignment with regulatory requirements and industry best practices.
  • Engage actively in professional development activities, including industry seminars, certification programs, and ongoing training.


Qualifications and Experience:


  • Bachelor's degree or higher in a scientific discipline or an equivalent combination of education and experience.
  • Minimum of 5 years of Quality Assurance experience, specifically within GLP-regulated environments, including experience in a supervisory or management role.
  • Professional certification such as RQAP-GLP (Registered Quality Assurance Professional-GLP) or ASQ-CQA (Certified Quality Auditor) strongly preferred.
  • Proven experience managing QA teams, leading audits, managing investigations, and independently hosting client or regulatory audits in a contract research organization
  • Familiarity with computerized system validation processes and requirements is advantageous.
  • Comprehensive understanding of the preclinical drug development process and associated regulatory expectations.


Skills and Competencies:


  • Strong leadership and team management capabilities.
  • Excellent organizational, problem-solving, and decision-making skills.
  • Exceptional communication and interpersonal abilities, able to effectively engage stakeholders across all organizational levels.
  • High level of detail orientation and ability to manage multiple tasks in a fast-paced environment.
  • Proficiency with Microsoft Office Suite and QA documentation management systems.


Join Our Team: If you're an experienced Quality Assurance professional passionate about leading teams and driving compliance excellence, we invite you to apply. Become a key leader in our organization, ensuring the integrity and quality of groundbreaking preclinical research.