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Contract Method Validation Jobs in Trevor, WI (NOW HIRING)

Technical Program Manager -- Firmware

Mundelein, IL · On-site

$131K - $170K/yr

... validation, production release, and sustaining. Note: this is an ONSITE role in Foster City, CA ... Establish structured processes and reporting methods that improve execution across fast-moving ...

New

This is a remote contract-to-hire opportunity with the potential for long-term employment. The ... Assign and validate Diagnosis-Related Groups (DRGs) * Ensure compliance with federal regulations ...

Contract * On-Site Required * 10+ years' of strong validation experience. * Software Quality ... Knows the difference between Waterfall and Agile software development methodologies. * Previous ...

Contract - * Strong background in mechanical engineering principles combined with elite-level ... Feasibility & Validation: Conduct rigorous Robot Reachability studies and Payload Analysis ...

Showing results 41-60

Contract Method Validation information

See Trevor, WI salary details

$22

$51

$77

How much do contract method validation jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for contract method validation in Trevor, WI is $51.34, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $62.40 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.

Analytical Chemistry (2-4 Yrs of Req Exp in pharmaceutical) - Onsite

Millenniumsoft, Inc

Vernon Hills, IL • On-site

$96.43/hr

Other

Posted 3 days ago

New


Job description

Position : Analytical Chemistry (Req Exp in pharmaceutical) Location : Vernon Hills, IL Duration : 12 Months 1st Shift Total Hours/week : 40.00 Client : Medical Devices Company Job Category : Industrial Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT) Rate of pay $35.79 Onsite Segment/Department Name: Infection Prevention, Analytical Chemistry Job Description - Purpose of Position:
  • This position provides analytical chemistry support and/or remediation to all chemistry-related projects for BD products currently on the market as well as new product development. This position will also participate in the conduct of the stability testing program to support the approval of process and/or product design changes. As needed, this position also supports the development and validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.
General Functions, Specific Responsibilities, and Authority:
  • Chemistry & performance testing, data review and entry, protocol/report generation, laboratory maintenance and support.
Knowledge, Education, and Skills Required: Education
  • BS/MS in Chemistry / Pharmaceutics with related science experience
Skills
  • Demonstrates developed knowledge of respective scientific discipline and standard scientific method and techniques.
  • Excellent scientific writing skills.
  • Ability to multi-task various activities.
  • Troubleshoot issues that arise and solve problems.
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Experience
  • 2-4 years' experience in pharmaceutical analytical chemistry is essential.
  • Hands-on experience with wet-chemistry and instrumental techniques (i.e. pH, tritration, UV-Vis, GC, HPLC).
  • Experience in working within an FDA regulated environment and GMP documentation requirements.
Specialized Knowledge
  • Ability to discuss scientific strategies/results and interact with other functional areas, including Regulatory, Manufacturing, and Quality.
  • Previous experience with writing scientific protocols and reports.
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