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Laboratory Technician

Sterling Engineering

Location

Buffalo Grove, IL

Salary

Not specified

Type

fulltime

Posted

Today

via linkedin

Job Description

Lab Technician

Buffalo Grove, IL

8-hour Shifts available:

  • 1st Shift, Mon-Fri (7am-3:30pm)
  • 2nd Shift, Mon-Fri (3pm-11:30pm)

12-hour Rotating Shifts Available: (2/2/3 schedule)

  • Day shift, 6am-6pm
  • Night Shift, 6pm-6am

Starting Pay $20\.50-$35/hour, depending on experience and shift.

  • Overtime Pay X1\.5/hr

Position Overview

The Quality Technician / Lab Technician will support a newly established wet chemistry laboratory focused on testing and validation of blood-reading medical devices. This role is responsible for executing laboratory testing, environmental monitoring, and quality control activities to ensure compliance with FDA, GMP, and internal quality standards.

This is a hands-on role in a highly regulated environment, requiring strong attention to detail, documentation accuracy, and the ability to follow structured test methods and protocols.

Key Responsibilities

  • Perform routine wet chemistry and microbiological testing to support validation and quality control of blood-reading devices
  • Execute laboratory activities including sample preparation, testing, data collection, and result reporting
  • Conduct microbiological testing such as bioburden, endotoxin, and media assessments
  • Perform environmental monitoring within controlled lab environments (viable air sampling, surface testing, etc.)
  • Support dosimetry and lab-controlled measurement activities where applicable
  • Inspect incoming materials, in-process samples, and finished components to ensure compliance with specifications
  • Identify, document, and escalate out-of-specification (OOS) or out-of-trend results
  • Assist with investigations, including root cause analysis and corrective actions (CAPA)
  • Maintain accurate, detailed, and compliant laboratory documentation following Good Documentation Practices (GDP)
  • Support lab startup activities including equipment setup, calibration, validation, and organization
  • Ensure adherence to GLP, GMP, FDA, ISO, and internal quality standards
  • Maintain cleanliness and organization of the laboratory environment in accordance with controlled lab requirements
  • Collaborate cross-functionally with Quality Engineers, Lab Management, and manufacturing teams

Qualifications

  • High School Diploma required; Associate’s or technical degree in Biology, Chemistry, or related field preferred
  • 2–5\+ years of experience in a laboratory, quality, or regulated manufacturing environment (medical device, pharma, or biotech strongly preferred)
  • Experience with wet chemistry or microbiology testing preferred
  • Familiarity with FDA-regulated environments and standards (GMP, GLP, ISO)
  • Experience with environmental monitoring and controlled lab environments is a plus
  • Strong documentation skills with high attention to detail
  • Ability to follow detailed procedures and work instructions with precision
  • Basic math skills (fractions, percentages, measurements)
  • Proficiency with Microsoft Office; experience with LIMS systems is a plus
  • Ability to work independently after training while maintaining high quality standards

Key Traits for Success

  • Detail-oriented with strong organizational skills
  • Ability to manage multiple tasks in a structured lab environment
  • Critical thinking and problem-solving mindset
  • Strong communication skills and ability to work within cross-functional teams
  • Comfortable working in a fast-paced, evolving lab environment (especially during lab buildout and FDA remediation efforts)

What This Role Offers

  • Opportunity to be part of a newly built lab supporting critical FDA remediation efforts
  • Hands-on involvement in medical device validation and quality systems
  • Exposure to cross-functional engineering and quality teams
  • Growth potential within quality, lab operations, or engineering pathways

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