Quality Control Engineer II – Microbiology

Oxoid Remel Microbiology (Acquired from Thermo Fisher Scientific); Lenexa (KS); On-site; USD 65,000 - 88,000; Full time

Job summary

Oxoid Remel Microbiology seeks an Engineer/Scientist II to support the Quality Control Organisms Laboratory in Lenexa, Kansas, focusing on finished-product testing, regulatory compliance, and continuous improvement. You will ensure products meet testing standards, IFUs, SOPs, and regulatory guidelines while collaborating with QC leadership.

The role combines hands-on testing with documentation review, root-cause investigations, and process improvements, requiring teamwork and adherence to GLP,

Qualifications

• Bachelor's degree in Biological Sciences or related field.
• Experience in a microbiology laboratory environment.
• Familiarity with FDA regulations for medical devices.
• Understanding of USP and CLSI requirements.
• Strong organizational and time management skills.
• Proficiency in MS Office.
• Ability to follow written and verbal instructions and lab procedures.
• Strong analytical, critical-thinking, and problem-solving skills.
• Excellent written and verbal communication in English.

Responsibilities

• Support finished-product testing and laboratory investigations.
• Review and maintain product compliance specifications and lab documentation.
• Ensure testing activities follow SOPs and regulatory requirements.
• Maintain accurate lab records for traceability and compliance.
• Collaborate with QC leadership and cross-functional teams on investigations and improvements.
• Develop and execute protocols supporting productivity and process improvement.

Skills

English communication

Analytical skills

Team collaboration

Documentation

Time management

Education

Bachelor's degree in Biological Sciences

Bachelor's degree in Microbiology

Tools

MasterControl

SAP

Microsoft Office

Job description

Oxoid Remel Microbiology seeks an Engineer/Scientist II to support the Quality Control Organisms Laboratory in Lenexa, Kansas, focusing on finished-product testing, regulatory compliance, and continuous improvement. You will ensure products meet testing standards, IFUs, SOPs, and regulatory guidelines while collaborating with QC leadership.

The role combines hands-on testing with documentation review, root-cause investigations, and process improvements, requiring teamwork and adherence to GLP,