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Quality Control Micro Jobs (NOW HIRING)

Legend Biotech USA, Inc.

Test method verification, qualification, validation and/or transfer activities in the QC Micro laboratories.Process Performance Qualification and Continued Process Verification activities associated ...

Integrity Trade Services

Quality Control

Buchanan, MI

$16 - $18/hr

Quality Control - $16.00-$18.00/HR Integrity Trade Services is hiring a Quality Control for our ... Conduct gaging and physical measurements utilizing, calipers, micrometers, Micro-Vu, optical ...

Integrity Trade Services

Quality Control

Buchanan, MI · On-site

$16 - $18/hr

Quality Control - $16.00-$18.00/HR Integrity Trade Services is hiring a Quality Control for our ... Conduct gaging and physical measurements utilizing, calipers, micrometers, Micro-Vu, optical ...

Newly Weds Foods

Quality Control Technician

Mount Pleasant, TX · On-site

$15.75 - $20.25/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 ...

Summa

QC Inspector

Houston, TX

$20 - $25/hr

... 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 ...

Actalent

Quality Control Technician

Chicago, IL · On-site

$19.25 - $24.75/hr

Quality Control Technician The Quality Control Technician evaluates finished products to ensure ... Collect microbiological (micro) samples as needed and place associated products on micro hold when ...

W3Global Inc.

Quality Control Inspector

Billerica, MA

$65K - $80K/yr

Full Quality Control Inspector Summary of Position: We are seeking an experienced mechanical ... Micro-Vu, Keyence, or similar vision system experience desired * Experience using standard ...

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How much do quality control micro jobs pay per hour?

As of May 31, 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 are the key skills and qualifications needed to thrive as a Quality Control Microbiologist, and why are they important?

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 are Quality Control Microbiologists?

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 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.

More about Quality Control Micro jobs
What cities are hiring for Quality Control Micro jobs? Cities with the most Quality Control Micro job openings:
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Quality Control Micro jobs near you
Infographic showing various Quality Control Micro job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 98% Full Time, and 1% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Sr. Manager, QC Microbiology

Legend Biotech US

Raritan, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a Sr. Manager, QC Microbiology as part of the Quality team based in Raritan, NJ.
Role Overview
The Sr. Manager, QC Microbiology, is an exempt level position with responsibilities for managing the operation and workflow of the quality control microbiology laboratories in support of cell therapy manufacturing. This includes hiring, development and performance management of staff, reviewing/approving laboratory test data, developing and implementing microbiology procedures and methods, supporting laboratory investigations and ownership of various QC microbiology department projects. The role develops and implements long-term strategies and manages a team of people leaders and technical professionals within the QC department based on assigned work, direction, coaching and developing capabilities
Key Responsibilities
  • Ensuring adequate training (skills-based, cGMP and safety) of people leaders and associates within the department.
  • Manage Raw material, in-process, environmental monitoring/utility, product release, and stability testing.
  • Manage and support Investigation of laboratory non-conformances (events, deviations, and invalid assays).
  • Maintenance, calibration and qualification of laboratory instruments and equipment.
  • Test method verification, qualification, validation and/or transfer activities in the QC Micro laboratories.
  • Process Performance Qualification and Continued Process Verification activities associated with QC microbiology laboratory testing.
  • Providing expertise in troubleshooting complex laboratory issues and demonstrating strong reasoning skills in support of ongoing laboratory investigations.
  • Maintain detailed knowledge of industry guidelines/trends, regulatory requirements, and applicable pharmacopeia while remaining current in on-the-job training requirements.
  • Collaborate with Quality Assurance, Manufacturing, Technical Operations, Engineering and Maintenance to support business needs.
  • Contribute to global strategies related to QC laboratories which align with compliance and business objectives as well as the overall corporate vision.
  • Manage departmental budget and resources; prepare staffing plans. Make adjustments to roles and responsibilities of department to meet business needs.
  • Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
  • Monitor QC method performance through trending analysis for on QC generated test results.
  • Represent department during internal and external audits.
  • Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals.
  • Works in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, Technical Operations, Engineering and Maintenance, Supply Chain and Planning.
  • Other duties will be assigned, as necessary.

Requirements
  • A minimum of a Bachelor's Degree in Science, Biology or equivalent technical discipline is required.
  • A Minimum of 12 to 14 years relevant work experience is required. It is preferable that the candidate has experience working in an aseptic manufacturing facility, preferably in microbiology quality control laboratory, quality assurance, or cell therapy. A minimum of 3-5 years of leadership experience is also required.
  • Experience working with Quality systems is required.
  • Extensive knowledge of chemical, biochemical and microbiological concepts is required.
  • Ability to apply basic and advanced mathematical concepts (including statistics) in the evaluation of laboratory data is required.
  • Knowledge of cGMP regulations and FDA/EU guidance is required.
  • Comfortable with speaking and interacting with inspectors.
  • Good written and verbal communication skills are required.
  • This position may require up to 10% domestic or international travel as business demands.
  • Detailed knowledge and understanding of current Good Manufacturing Practices (cGMP) and current Good Tissue Practices (cGTP) related to CAR-T manufacturing or cell processing.
  • Proven people management and leadership experience are required.
  • In-depth knowledge and experience in biopharmaceutical analysis method verification is preferred.
  • Experience in microbiological test methods and EM is preferred.
  • Ability to quickly process complex information and often make critical decisions with limited information.
  • Ability to handle multiple priorities on a daily basis while being flexible and responsive to frequently shifting priorities.
  • Proficient in applying excellence tools and methodologies.
  • Ability to summarize and present results, and experience with team-based collaborations is a requirement.
  • Experience in developing and setting long-term objectives for individual and teams.
  • Have a high sense of responsibility and professionalism with excellent organizational skills, analytical judgment and communication skills.
  • Able to work cross functionally and under pressure.

#Li-BZ1
#Li-Onsite
The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.
Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.
Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
Pay Range (Base Pay):
$146,410-$192,164 USD
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.
EEO Statement
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.
For information related to our privacy notice, please review: Legend Biotech Privacy Notice.

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