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Qc Microbiology Supervisor Jobs (NOW HIRING)

QC Microbiology Technician

Frederick, MD · On-site

$25.25 - $33.25/hr

Title: QC Microbiology Technician Duration: 12 months contract Location: Frederick, MD 21704 Shift: Wednesday to Saturday, 7:00 AM - 6:00 PM Position Summary • We are seeking a highly motivated ...

New

R&D Partners is seeking to hire a Quality Control Microbiology Tech in Frederick, MD . Your main responsibilities as a Quality Control Microbiology Tech: · Maintain laboratory areas in a clean ...

Associate Director, QC Microbiology

Hopewell, VA · On-site

$22.75 - $30/hr

Leads and manages all QC Microbiology laboratory activities to support GMP manufacturing, including Environmental Monitoring (EM) and microbiological testing of materials, intermediates, and finished ...

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Qc Microbiology Supervisor information

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$47K

$93.7K

$145K

How much do qc microbiology supervisor jobs pay per year?

As of Sep 2, 2026, the average yearly pay for qc microbiology supervisor in the United States is $93,656.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $111,000.00 per year, depending on experience, location, and employer.

What does a QC Microbiology Supervisor do?

A QC Microbiology Supervisor oversees the microbiology laboratory operations within a quality control environment, ensuring that testing procedures comply with regulatory standards and company policies. They manage a team of microbiologists, review test results, and troubleshoot any microbial contamination issues. Additionally, they collaborate with other departments to support product quality, conduct investigations, and implement process improvements. Their role is critical in maintaining compliance with Good Manufacturing Practices (GMP) and ensuring product safety.

What are the key skills and qualifications needed to thrive as a QC Microbiology Supervisor?

To excel as a QC Microbiology Supervisor, you need a robust background in microbiology or a related life science, experience in quality control, and a bachelor's or advanced degree. Familiarity with laboratory information management systems (LIMS), aseptic techniques, GMP regulations, and certifications like ASQ or similar are highly beneficial. Strong leadership, communication, problem-solving, and organizational skills distinguish outstanding supervisors in this field. These capabilities are critical to ensure regulatory compliance, maintain product safety, and lead high-performing QC teams in a laboratory environment.

What are the typical daily responsibilities of a QC Microbiology Supervisor?

A QC Microbiology Supervisor oversees the daily operations of the microbiology laboratory, ensuring all testing is conducted according to established protocols and regulatory standards. This includes supervising laboratory staff, reviewing and approving test results, troubleshooting technical issues, and maintaining laboratory documentation for audits. The role also often entails training team members, coordinating with other quality departments, and participating in investigations of out-of-specification results. By balancing technical duties with team leadership, the supervisor ensures high-quality and timely support for manufacturing processes.

More about Qc Microbiology Supervisor jobs

What cities are hiring for Qc Microbiology Supervisor jobs?

Cities with the most Qc Microbiology Supervisor job openings:

What states have the most Qc Microbiology Supervisor jobs?

States with the most job openings for Qc Microbiology Supervisor jobs include:

Infographic showing various Qc Microbiology Supervisor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $93,656 per year, or $45 per hour.

Microbiology Analyst I

Nephron Pharmaceuticals

West Columbia, SC • On-site

Full-time

Re-posted 15 days ago


Job description

Job Purpose:
The QC Microbiology Analyst I performs microbiology department related raw material, in-process, and finished product testing according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Must demonstrate a high level of proficiency in Microbiology testing.
Essential Duties and Responsibilities:
• Applies quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures.
• Notifies Microbiology management of all OOS and OAL testing results.
• Provides feedback on SOPs, forms, logbooks, etc., as necessary, to facility ever-changing expectations for operating procedures and testing-related information.
• Performs routine testing of products to support release and company needs.
• Trains fellow QC laboratory personnel on QC test methods.
• Demonstrates ability to understand and interpret test results in relation to acceptance or rejection of lot tested.
• Generates data, as needed, for investigations; performs data entry for various systems and processes, and understands the necessity of trending reports
• Reports and initiates documentation and communication of OOS and OOT results and investigation reports.
• Assists the Sample Management team with sample receiving and waste destruction, as needed.
• Performs method validation testing if requested by supervisor.
• Performs general laboratory housekeeping and upkeep of various testing stations.
• Communicates all Microbiology-related observations, issues, problems, discrepancies, and any violation of company policies or procedures to QC Microbiology Shift Lead, QC Microbiology Supervisor, QC Microbiology Operations Manager, Director of Microbiology, or designee.
Supplemental Functions:
  • Performs other duties as assigned.

Job Specifications and Qualifications:
Knowledge & Skills:
  • 2 - 4 years of experience with Microsoft Office programs, as well as the ability to learn new systems and computer software programs effectively and efficiently required.
  • Experience with cGMP documentation systems and with implementation of quality control systems.
  • Strong interpersonal, verbal, and written communication skills; effectively multi-tasking and problem solving skills.
  • Must maintain flexibility in the assignments of tasks, and be open to receive and provide training in multiple areas.
  • Knowledge of FDA manufacturing/regulatory quality systems regulations, qualifications, facilities, and requirements.
  • Accepting of new changes in order to achieve department demands.
  • Must possess effective written and oral communication skills and be able to handle multiple tasks within limited time frames.
  • Aseptic technique and familiarity with cGMPs and regulatory requirements is required.
  • Specific expertise, skills and knowledge within microbiology gained through education and experience.
  • A broad perspective that aligns decisions to organizational objectives and long term consequences of day-to-day activities.
  • The ability to take strategic objectives and accept accountability to drive results through effective actions.
  • The ability and willingness to change direction and focus to meet shifting organizational and business demands.
  • The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.
  • Position requires bending, typing, lifting, reaching, vision, standing (50%), sitting (10%), walking (20%), and hearing.
  • Incumbents required to wear safety glasses, gloves, laboratory coats and other non-specified protective equipment as necessary.

Education/Experience:
  • Regionally accredited Bachelor's Degree in Biology, Microbiology, or Life Sciences, required; Master's degree, preferred.

• At least 1-year experience working directly with Pharmaceutical Microbiology methods.
• 1 - 2 years of experience in general laboratory skills and a knowledge of aseptic technique.
Working Conditions / Physical Requirements:
  • This position requires bending, typing, lifting (up to 40 1bs.), standing, sitting and walking throughout the facility.

• Hours of work: 12-hour rotating shifts.
• Salary range: Based on experience.