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Quality Control Analyst Microbiology Jobs (NOW HIRING)

Astrix Inc

Quality Control Analyst I/III

Thousand Oaks, CA · On-site

$39.90 - $60.10/hr

... Manufacturing, Microbiology, and external testing partners. Candidate level placement will be ... Support QC laboratory testing using standard analytical techniques including pH, Osmolality, and FT ...

ARUP Laboratories

Quality Control Analyst

Salt Lake City, UT · On-site

$23.25 - $31.25/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

Lonza

QC Analyst I-Microbial Control

Portsmouth, NH

$24.50 - $32.75/hr

Portsmouth, NH, (On-site) As a QC Analyst I in Microbial Control at our Portsmouth site, you will support microbiological testing and monitoring activities to help ensure the safety and quality of ...

ARUP Laboratories

Quality Control Analyst

South Jordan, UT · On-site

$22.75 - $30.50/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

Lonza

QC Analyst I-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Portsmouth, NH, (On-site) As a QC Analyst I in Microbial Control at our Portsmouth site, you will support microbiological testing and monitoring activities to help ensure the safety and quality of ...

Lonza

QC Analyst II-Microbial Control

Portsmouth, NH

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC ... You will perform microbiological testing, support environmental and utility monitoring, and deliver ...

Intellectt INC

QC Analyst

Lebanon, IN · On-site

$23 - $31/hr

My name is Vyshu, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a QC Analyst - Master Data (LI MS) based in Lebanon, IN with one of our prestigious clients.

Lonza

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC ... You will perform microbiological testing, support environmental and utility monitoring, and deliver ...

InstantServe LLC

QC Microbiology Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Quality Control/Testing: I Duration: 5+ Months Location: Durham NC USA 27712 Description of Responsibilities Position Summary The QC Microbiology Analyst 1 role is responsible for microbiological ...

Arixa Capital

QC Analyst

Los Angeles, CA · On-site

$25.75 - $34.75/hr

Position Overview The QC Analyst is an analytical, process driven, and detail-oriented professional responsible for supporting Arixa Capital's data quality across the loan lifecycle. This role ...

Arixa Capital

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and provide feedback and training to the operational teams to avoid future inconsistencies. This position ...

Arixa Capital

QC Analyst

Phoenix, AZ · Hybrid

$23.75 - $32/hr

The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and provide feedback and training to the operational teams to avoid future inconsistencies. This position ...

Arixa Capital

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

Position Overview The QC Analyst is an analytical, process driven, and detail-oriented professional responsible for supporting Arixa Capital's data quality across the loan lifecycle. This role ...

Granules

Biochemist I/II (QC Analyst)

Chantilly, VA · On-site

$55K - $80K/yr

The role of Biochemist I/II (QC Analyst) is responsible for supporting the operations and ... Conduct routine analytical/microbiological testing of raw materials, packaging materials, finished ...

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Quality Control Analyst Microbiology information

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How much do quality control analyst microbiology jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for quality control analyst microbiology in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What does a Quality Control Analyst Microbiology do?

A Quality Control Analyst in Microbiology is responsible for testing and analyzing samples to ensure that products meet established microbiological quality and safety standards. They perform various laboratory tests to detect microorganisms such as bacteria, fungi, and viruses in pharmaceutical, food, or other product samples. Their role also involves documenting results, maintaining laboratory equipment, and ensuring compliance with regulatory guidelines. By identifying potential contaminants, they help prevent unsafe products from reaching consumers.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst Microbiology, and why are they important?

A Quality Control Analyst Microbiology needs a solid background in microbiology, laboratory techniques, and a relevant degree such as microbiology, biology, or a related field. Familiarity with laboratory equipment, aseptic techniques, LIMS (Laboratory Information Management Systems), and regulatory standards like GMP is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts excel in identifying and reporting issues accurately. These competencies ensure reliable testing, regulatory compliance, and product safety in pharmaceutical or food production environments.

What is the difference between Quality Control Analyst Microbiology vs Quality Control Analyst Chemistry?

AspectQuality Control Analyst MicrobiologyQuality Control Analyst Chemistry
Required CertificationsMicrobiology certifications, such as ASM or microbiology-specific trainingAnalytical chemistry certifications, such as ASCP or chemistry-specific training
Work EnvironmentLaboratories focused on microbiological testing, sterile environmentsLaboratories performing chemical analysis, instrumentation-based testing
Industry UsagePharmaceutical, biotech, food safety industriesPharmaceutical, chemical manufacturing, environmental testing

Both roles involve quality testing but focus on different types of analysis. Microbiology analysts specialize in microbial detection and contamination control, while chemistry analysts focus on chemical composition and purity. They share similar certifications and work environments but serve distinct industry needs.

What are some common challenges faced by Quality Control Analysts in Microbiology and how can they be managed?

Quality Control Analysts in Microbiology often face challenges such as maintaining strict aseptic techniques to avoid contamination, staying current with evolving regulatory standards, and ensuring accurate, timely documentation of results. Managing these challenges typically involves regular training, adherence to standard operating procedures, and effective communication with cross-functional teams, such as production and quality assurance. A proactive approach to troubleshooting and continuous improvement is also essential for success in this role.
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Quality Control Analyst Microbiology jobs near you
Infographic showing various Quality Control Analyst Microbiology job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 86% Full Time, 6% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.
Quality Control Analyst I/III

Quality Control Analyst I/III

Astrix Inc

Thousand Oaks, CA • On-site

$39.90 - $60.10/hr

Full-time, Contractor

Posted 25 days ago

Job description

Pay Rate Low: 28 | Pay Rate High: 60
Quality Control Analyst I / III
Pharmaceutical / Biopharmaceutical Manufacturing | 6-month Contract
Position Overview
A leading contract development and manufacturing organization (CDMO) is seeking Quality Control Analysts at two levels to support cGMP laboratory operations. These roles are integral to ensuring product quality, data integrity, and regulatory compliance across in-process, finished product, and stability testing programs.
Both levels operate within a structured QC laboratory environment and contribute to cross-functional initiatives involving Quality Assurance, Manufacturing, Microbiology, and external testing partners. Candidate level placement will be determined based on relevant experience and technical skillset.
Position Details
Location: On-site in Santa Rosa, CA
Employment Type: 6-month contract with potential for extension or conversion
Hours: M-F 8-5
Compensation
Level Pay Range QC Analyst I $27.40 - $41.35/hr QC Analyst II $39.90 - $60.10/hr
Core Responsibilities (All Levels)
  • Support QC laboratory testing using standard analytical techniques including pH, Osmolality, and FT-IR instrumentation for in-process, finished product, and stability sample analysis.
  • Perform accurate documentation and data recording in accordance with cGMP principles, ALCOA+ standards, and data integrity requirements.
  • Assist with laboratory investigations including out-of-specification (OOS) results, deviations, invalid assays, and other quality system activities.
  • Assist with sample management activities including sample login, labeling, tracking, storage, and shipment coordination.
  • Support stability program execution including sample pulls, submissions, inventory management, and tracking activities.
  • Follow approved SOPs, test methods, and GMP laboratory procedures with appropriate supervision.
  • Perform self-review of data and documentation for accuracy and completeness prior to submission for secondary review.

Level-Specific Responsibilities
QC Analyst I
The QC Analyst I functions in a support capacity within the laboratory, performing routine and standardized testing activities under closer direction. This role is well-suited for candidates early in their analytical career who are building foundational GMP laboratory skills.
  • Execute routine laboratory testing using established methods and SOPs with minimal supervision.
  • Perform data entry into relevant data management systems with accuracy and attention to detail.
  • Assist with day-to-day laboratory support activities as directed by senior laboratory personnel.

QC Analyst III
The QC Analyst III operates at a higher level of independence and technical complexity, taking on expanded responsibilities in method execution, investigation leadership, and cross-functional collaboration. This role is suited for candidates with prior cGMP analytical experience seeking to broaden their scope.
  • Perform complex analytical testing including HPLC, ELISA, and other advanced techniques with independent data evaluation.
  • Troubleshoot equipment issues promptly and communicate resolutions to management.
  • Evaluate data for trends and compile data summaries for management review and reporting.
  • Support and/or lead investigations of OOS events through thorough root cause analysis, assessment of potential product impact, and implementation of appropriate corrective and preventive actions (CAPAs).
  • Interact with cross-functional departments including attendance at meetings and provision of testing updates.
  • Coordinate testing performed at outside testing laboratories including raw materials and external analytical services.
  • Execute, author, and review SOPs, protocols, reports, investigations, change controls, and data summaries.
  • Write and revise test methods and standard operating procedures in alignment with regulatory expectations.
  • Provide training to junior laboratory personnel; attend internal and external training on relevant techniques and procedures, including intra- and inter-departmental cross-training.
  • Enter, track, and trend data within relevant data management systems; present data summaries to management.
  • Lead the stability program including management of test points, reporting of data, and investigation of out-of-specification or aberrant stability results.

Qualifications
QC Analyst I
  • Bachelor's degree in Chemistry, Biology, Biochemistry, or a related life science discipline
  • 0 to 2 years of relevant laboratory experience; prior cGMP exposure is a plus
  • Familiarity with basic analytical instrumentation (e.g., pH meter, Osmometer, FT-IR)
  • Working knowledge of GMP documentation practices and data integrity principles
  • Strong attention to detail and ability to maintain accurate records
  • Ability to follow written procedures and verbal instructions in a structured laboratory environment

QC Analyst II
  • Bachelor's degree in Chemistry, Biology, Biochemistry, or a related life science discipline; advanced degree a plus
  • Minimum 2 to 4 years of relevant QC laboratory experience in a cGMP-regulated pharmaceutical or biopharmaceutical environment
  • Hands-on experience with complex analytical techniques including HPLC and/or ELISA
  • Demonstrated ability to independently plan, execute, and evaluate laboratory investigations and OOS events
  • Experience authoring or reviewing GMP documents including SOPs, protocols, reports, and change controls
  • Experience with data management systems and trending/tracking activities preferred
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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