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Quality Control Micro Jobs (NOW HIRING)

Pine Pharmaceuticals

QC Micro Analyst II

Tonawanda, NY · On-site

$24/hr

This position collaborates closely with Quality Assurance, Manufacturing, and Quality Control management while maintaining accurate documentation, promoting a safe laboratory environment, and ...

Kellton Tech

QC Micro EM Analyst II

Houston, TX · On-site

$25 - $33/hr

Quality Control Environmental Monitoring Technician Location: Houston, TX (Onsite) Pay Range: $25-33/hr. on W2 Shift: 1st Shift (Wednesday - Saturday) Experience Required: * 3-5 years of relevant ...

Newly Weds Foods

Quality Control Manager

Gerald, MO · On-site

Oversee food defense and security, sanitation, pest control, micro-testing and water quality maintenance. * Perform mock recalls. * Review Quality Control or vendor deviations. * Assist Regulatory ...

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How much do quality control micro jobs pay per hour?

As of Jul 13, 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 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 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 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.

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.
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Quality Control Micro jobs near you
Infographic showing various Quality Control Micro job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.
Job Title: Senior Manager QC Microbiology, (Hopewell, NJ)

Job Title: Senior Manager QC Microbiology, (Hopewell, NJ)

BeiGene, Inc.

Hopewell, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
Manages all QC Microbiology Environmental Monitoring (EM) as well as the utilities sampling programs for WFI, Clean Steam, and Process Gases in accordance with FDA/EU regulations, applicable International Regulations, and BeOne processes and procedures. Oversees and implements QC Microbiology procedures. Authors and reviews QC Microbiology Deviations and Trend Reports. Supports commissioning and qualification of new laboratory equipment. Supports regulatory compliance inspections. Ensures efficient and effective day-to-day operations of the Microbiology laboratory.
Essential Functions of the job:
  • Lead the Environmental Monitoring (EM) and Utilities Sampling programs in accordance with FDA/EU regulations and applicable International Regulations.
  • Compile, author and review QC Trend Reports for Environmental and Utilities Monitoring.
  • Build a highly efficient QC microbiology team, identify and develop key talents.
  • Oversee gowning and aseptic qualifications for site wide personnel.
  • Author and review QC Microbiology Deviations, CAPAs and Change Controls.
  • Lead QC Microbiology laboratory activities to support GMP manufacturing and microbiological testing of materials, intermediates, and finished products in accordance with FDA/EU regulations.
  • Manage QC Micro-Lab routine operations, including but not limited to microbiological sampling, testing, data review, personnel training, and equipment maintenance.
  • Ensure Micro-Lab EHS compliance.
  • Ensure timely completion of sampling (EM, WFI, Clean Steam, and Process Gases) to support QC testing as well as to ensure timely generation and reporting of test results in support of manufacturing operations.
  • Ensure appropriate investigation of OOS events and Microbial Data Deviations (MDD).
  • Ensure appropriate corrective actions and preventive actions (CAPAs) are implemented to prevent recurrence of OOS and MDDs.
  • Participate in internal and external GMP audits.
  • Manage microbial method verification activities, including the verification strategy and approval of protocols and reports.
  • Ensure that the QC Micro-Lab meets or improves on budget, cost, volume and efficiency targets (KPIs) in line with business objectives.
  • Introduce advanced concept of microbiology laboratory to keep the laboratory forward-looking and competitive in the industry.
  • Manage, motivate, coach and mentor direct reports.
  • Undertake any other duties as required.
  • Interacts with all levels of BeOne employees.

Required Education / Experience:
  • Bachelor's Degree or above in Microbiology or Biotechnology related scientific discipline. Scientific degree (ideally microbiology, pharmaceutical sciences, biotechnology or related).
  • Minimum of 7 years' experience in biological drug product Quality Control in a FDA-regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required.
  • Minimum of 5 years' experience in management, with training and knowledge of Data Integrity Guidance and Data Management Systems utilized in a Quality Operation
  • Expert in environmental monitoring, utilities sampling, pharmaceutical microbial testing and related equipment/instruments.
  • Familiar with the USP/EP and cGMP/EU GMP regulations.
  • Experience with microbial contamination control of aseptic process.
  • Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
  • Wide knowledge of analytical methods and electronic systems (LIMS, MODA) used in the QC Micro-Lab.
  • Strong leadership/team management skills and experience.
  • Credible and confident communicator (written and verbal) at all levels.
  • Strong analytical and problem-solving ability.
  • Excellent project management skills.
  • Hands-on approach, with a 'can do' attitude.
  • Ability to prioritize, demonstrating good time management skills.
  • Excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
  • Self-motivated, with the ability to work proactively using own initiative.
  • Committed to learning and development.

Supervisory Responsibilities:
  • Manage direct reports from QC Micro-Lab.

Computer Skills:
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint)

Travel:
  • Must be willing to travel approximately 10%
  • Ability to work on a computer for extended periods of time

Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $127,400.00 - $172,400.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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