Full-Time

Environmental Data Validation / Quality Assurance Lead

Posted on 12/12/2025

Deadline 9/3/26
Serco North America

Serco North America

No salary listed

Chicago, IL, USA

In Person

On-site in Chicago, IL; no hybrid option currently. Relocation assistance may be offered upon award.

Category
QA & Testing (1)
Requirements
  • BS/BA in Chemistry or related field from an accredited university
  • 8+ years in an environmental laboratory and/or using EPA methods (6 years with an MS, 4 years with a Ph.D)
  • Experience managing analytical or data validation chemists or quality assurance personnel
  • Expertise in Organic and Inorganic prep, analyses, and data review
  • Proficient in Microsoft Office 365
  • Strong analytical, communication, and leadership skills
  • Must be able to work on-site at the Chicago, IL Laboratory Monday through Friday. This position does not offer any Hybrid work schedules at this time
  • Ability to obtain EPA Public Trust
Responsibilities
  • Review and validate organic (volatiles, semi-volatiles, pesticides, PCBs) and dioxin/PCB congener data using USEPA National Functional Guidelines (NFGs) and Regional SOPs
  • Review and validate ICP/AES and ICP/MS metals data per NFGs
  • May require a familiarity with various other organic, inorganic and high-resolution mass spectrometry (HRMS) methods
  • Prepare detailed, professional reports on findings
  • Manage electronic data across platforms
  • Monitor workflow, backlogs, and performance metrics
  • Conduct SOP reviews as needed
  • Trend and monitor key performance metrics.
  • Technical support in development, review, and/or revision of QA-related documents which may include: statements of work, scopes of work, reporting procedures, functional guidelines, data validation manuals, and other data review guidance for various analytical procedures, technical papers/documents prepared for publication, etc.
  • Maintenance of laboratory-related documents including support to review, track, and maintain laboratory-related documents
  • Implementation of a QA Program including QMP, QAPPs, and related procedural SOPs
  • Generation and maintenance of documentation to keep current with program changes and to maintain efficiency.
Desired Qualifications
  • OSHA HAZWOPER 40-Hour certification
  • 2+ years as an organic and/or inorganic chemist or lab technician
  • First Aid/CPR/AED certification

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