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Quality Control Micro Jobs (NOW HIRING)

$18.75 - $24.75/hr

Job Summary The Principal Specialist - Quality Control Microbiology (QC Micro) Lead, will serve as the Lead for the Microbiology side of the QC unit at a large molecule manufacturing plant. This role ...

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Food defense and security, sanitation, pest control, micro-testing and water quality maintenance. Review Quality Control or vendor deviations. Assist Regulatory Technical Information Systems and ...

QC Tech

Pendleton, OR · On-site

$19 - $24.25/hr

Collect micro samples as needed and places micro hold products on hold. * Performs special tasks as assigned by QC manager. * Maintains retain sample area and control sample file. * Follows all GMP ...

QC Tech

Pendleton, OR

$19 - $24.25/hr

Collect micro samples as needed and places micro hold products on hold. * Performs special tasks as assigned by QC manager. * Maintains retain sample area and control sample file. * Follows all GMP ...

Manager, Quality Control

Carson, CA · On-site

$105K - $138K/yr

Manage Environmental Monitoring Program (EMP) swab testing for micro indicators, pathogens ... QC, Sanitation, and Operations personnel. * Lead and maintain BRCGS certification across all ...

... on incoming quality control. This role supports inspection of raw materials and precision ... This is a detail-heavy, precision-focused role working with small components like PCBs and micro ...

Quality Technician II, QC Aseptic

West Chester, OH · On-site

$17.50 - $22.25/hr

For more information, please visit www.resilience.com The Quality Technician II, QC Aseptic Control Micro - Aseptic Control Technician performs environmental monitoring and microbial sampling ...

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Quality Control Micro information

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How much do quality control micro jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for quality control micro in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is a quality control microbiologist?

Quality Control Microbiologists, often called QC Micro, are professionals who monitor and ensure the microbiological quality of products, environments, or processes, especially in industries like pharmaceuticals, food, and cosmetics. They conduct laboratory tests to detect and identify microorganisms, ensuring products meet safety and regulatory standards. Their work helps prevent contamination, ensures consumer safety, and maintains compliance with government regulations. QC Microbiologists also document results, analyze trends, and may be involved in troubleshooting and improving microbiological testing procedures.

What are the key skills and qualifications needed to thrive as a quality control microbiologist?

To thrive as a Quality Control Microbiologist, you need a solid background in microbiology, laboratory techniques, and a relevant degree in biology or a related field. Familiarity with laboratory information management systems (LIMS), aseptic techniques, and regulatory standards such as GMP are typically required, and some roles may prefer certifications like ASCP. Attention to detail, problem-solving abilities, and strong communication skills help ensure accuracy and effective teamwork in the lab. These competencies are crucial for maintaining product safety, regulatory compliance, and overall quality standards in manufacturing or clinical environments.

What are the typical challenges faced by a quality control microbiologist in a laboratory setting?

Quality Control Microbiologists often encounter challenges such as managing high sample volumes while maintaining accuracy, adapting to evolving regulatory standards, and troubleshooting unexpected contamination or equipment malfunctions. They must also balance timely result delivery with strict adherence to testing protocols and documentation requirements. Collaboration with production teams and other quality departments is essential to address issues promptly and ensure product safety and compliance.

What is the difference between Quality Control Micro vs Quality Control Inspector?

AspectQuality Control MicroQuality Control Inspector
CertificationsOften requires microbiology or lab certificationsTypically requires general quality assurance certifications
Work EnvironmentLaboratory settings, microbiology labsManufacturing plants, production lines
Industry UsageFood, pharmaceuticals, biotechManufacturing, consumer goods
Job FocusMicrobial testing, lab analysisProduct inspection, quality assurance

While both roles focus on quality assurance, Quality Control Micro specializes in microbial testing and lab analysis, often within laboratory environments. In contrast, Quality Control Inspectors typically perform on-site product inspections in manufacturing settings. Understanding these differences helps job seekers target the right roles based on their skills and industry interests.

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Infographic showing various Quality Control Micro job openings in the United States as of September 2026, with employment types broken down into 2% As Needed, 80% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Quality Control, Senior Associate Specialist (Weekend)

Cranbury, NJ • On-site

$28 - $42/hr

Other

Posted 29 days ago


Key responsibilities

  • Perform quality testing and sampling of environmental, water, gas, and raw materials according to GMP procedures.

  • Record, report, and analyze test results, including generating trend charts and reports.

  • Support investigation of out-of-specification results, conduct root cause analysis, and assist in preparing documentation such as SOPs, reports, and validation documents.


Job description

Job Title - Senior Assocaite Specialist, Quality Control (Weekend)
Work Location - Cranbury, NJ
Shift/Hours - 8:30am - 5pm - Saturday & Sunday required, 3 weekdays
Job Summary:
This team member (Weekend Shift) is responsible for the quality and on-time testing/collection of samples, EM (Environmental sampling), Water and Gas system sampling (when required) with raw material sampling to the various testing sections. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and GMP documentation.
Job Responsibilities:
  • Adhere to GMP sampling (Clean rooms, WFI, gas) and testing, follow laboratory procedures according to and in compliance with cGMP guidelines and internal SOPs.
  • Able to follow and conduct EM sampling in cleanroom areas in/between the various building sites in Cranbury or other US sites (when needed).
  • Able to support sample receiving, transporting needs in/between the various building sites in Cranbury or other US sites (when needed).
  • Perform micro related testing including but not limit to bioburden, pH, growth promotion, endotoxin, conductivity, TOC, nitrate, plate readings, plate transferring etc (when required).
  • Receive required samples, perform testing, report results independently and in a timely manner (when required).
  • Able to input data and generate EM data trend charts and reports.
  • Able to initiate investigation/excursions when having OOS/OOL/Atypical results
  • Able to perform reagents/consumables inventory management (LIMS receiving, disposal etc) to ensure consistent QC Micro operation needs..
  • Operate according to the experimental or sampling plan and deliver results, testing/sampling method/SOP's
  • Record and organize experimental data in accordance with "Good Document Management Practices" to ensure data integrity.
  • Ensure compliance to training, preparation, documentation and general lab maintenance requirements for Industry Standards and/or Regulations.
  • Assist in preparing SOP, protocols, final reports, investigations, and deviations as needed..
  • Assist in investigating any Out-of-Specification results and laboratory deviations, conducting root cause analysis, and implementing CAPA.
  • Assist in preparing or executing validation documents to support new materials, process changes and qualifications.
  • Maintains laboratory notebooks and worksheets for QC tasks as required.
  • Work for weekend shift (Wed to Mon, or Thur to Tue)
  • Support night shift work when required by supervisor (when needed)
  • Any other duties assigned by the supervisor (when applicable)

Job Qualifications:
Education and Experience:
  • High school certificate or above degree and/or advanced Graduate degree in Chemistry, Microbiology, Biochemistry or equivalent field.
  • High school certificate: 2 years and above working experience is preferred
  • Bachelor's degree: 1 year and above working experience is preferred
  • Master's degree: no requirement

Technical Skills / Knowledge:
  • Candidate must possess willingness to learn analytical and QC operations of pharmaceutical industry, understand current regulations and industry trends of biologics product development, characterization and manufacturing testing requirement including cGMP, ICH, EMA, FDA, and other global compendia regulations and guidance.
  • Basic familiarity with analytical instruments and methodologies, such as TOC, conductivity meter is preferred but not mandatory.
  • Basic experience with software and information systems (e.g. Empower, TrackWise, Master Control, LES, lab notebook and preferably LIMS). Ability to adapt between strategic and tactical thinking/planning and manage multiple priorities to achieve department and site objectives.
  • Ability to understand technical data

Problem Solving:
  • Basic experience in planning and ability to solve simple QC technical and operation problems.
  • Be able to raise issues immediately to supervisor and work with supervisor when in doubt.

Communication Skills:
  • Proficiency in English is required. Good communications skills (verbal, written, and presentation skills).
  • Effectively exchange information or discuss clearly framed issues or ideas with colleagues.

The anticipated hourly range for this position is $28 - $42hr
Job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.