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Manager Quality Control Microbiology Jobs (NOW HIRING)

RESILIENCE

Senior Analyst, QC Microbiology

West Chester, OH · On-site

$22.75 - $30.50/hr

... Analyst, QC Microbiology performs and documents microbiological testing on raw materials, in ... Facilitate communication between management and non-management and team meetings. * Provide ...

ProKidney

QC Microbiology Analyst 3

Winston Salem, NC · On-site

$22.25 - $29.75/hr

Quality Control (QC) Microbiology Analyst III provides support and execution on ProKidney ... Generate and present metrics and trends for Management Review. * Support training on Good ...

Alliance Biotech Solutions LLC

QC Microbiologist

Raleigh, NC · On-site

$22 - $28.75/hr

Experience/Skills • Bachelor's degree in Microbiology, Biology, Biotechnology, or a related life sciences field. • 3+ years of QC Microbiology experience in a pharmaceutical or biotech GMP ...

Perritt Laboratories

Be Seen First

Lead QC Microbiology Specialist

Hightstown, NJ · On-site

$70K/yr

... to oversee critical quality-control testing operations in our pharmaceutical microbiology ... Manage microbiological culture inventories and related laboratory resources * Communicate testing ...

Lonza

Senior Supervisor QC Microbiology

Vacaville, CA · On-site

$10K - $170K/mo

The Senior Supervisor, Quality Control Microbiology will lead laboratory personnel and manage day-to-day testing operations within a cGMP manufacturing environment. This role is responsible for ...

Integrated Resources INC

QC Microbiologist

Andover, MA

$25.75 - $34/hr

We deliver strategic workforce solutions that help you manage your talent and business more ... documentation respective to QC Microbiology assay and activities. Review will include:

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How much do manager quality control microbiology jobs pay per year?

As of Jul 2, 2026, the average yearly pay for manager quality control microbiology in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Manager Quality Control Microbiology, you need expertise in microbiological testing, regulatory compliance, and quality assurance, typically supported by a degree in microbiology or a related field. Familiarity with laboratory information management systems (LIMS), GMP/GLP regulations, and certifications such as ASQ Certified Quality Auditor are often required. Strong leadership, problem-solving, and communication skills help drive team performance and effective cross-departmental collaboration. These skills ensure accurate testing, regulatory adherence, and consistent product quality in pharmaceutical or biotech environments.

What does a Manager Quality Control Microbiology do?

A Manager Quality Control Microbiology oversees the microbiological testing and quality assurance processes in laboratories, typically within pharmaceutical, biotechnology, or food industries. They manage teams responsible for ensuring that products are free from harmful microorganisms and comply with regulatory standards. Their duties include establishing testing protocols, troubleshooting laboratory issues, training staff, reviewing data, and ensuring compliance with Good Manufacturing Practices (GMP). They also collaborate with other departments to resolve quality issues and implement continuous improvement initiatives. Effective managers in this role play a critical part in maintaining product safety and quality.

What are the typical challenges faced by a Manager Quality Control Microbiology, and how can they be addressed?

A Manager Quality Control Microbiology often faces challenges such as ensuring regulatory compliance, maintaining laboratory data integrity, and keeping up with evolving testing technologies. Managing a diverse team of microbiologists and coordinating with cross-functional departments like manufacturing and quality assurance also requires strong leadership and communication skills. Staying proactive with training, implementing rigorous quality systems, and fostering a culture of continuous improvement helps address these challenges effectively.
What cities are hiring for Manager Quality Control Microbiology jobs? Cities with the most Manager Quality Control Microbiology job openings:
What are the most commonly searched types of Quality Control Microbiology jobs? The most popular types of Quality Control Microbiology jobs are:
What states have the most Manager Quality Control Microbiology jobs? States with the most job openings for Manager Quality Control Microbiology jobs include:
Manager Quality Control Microbiology jobs near you
Senior Analyst, QC Microbiology

Senior Analyst, QC Microbiology

RESILIENCE

West Chester, OH • On-site

$22.75 - $30.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago

Job description

A career at Resilience is more than just a job - it's an opportunity to change the future.
Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
For more information, please visit www.resilience.com
Position Summary
The Senior Analyst, QC Microbiology performs and documents microbiological testing on raw materials, in-process and finished products, and environmental samples. The role ensures GMP compliance through timely review of laboratory data and documentation, communicates findings, and supports corrections. This position also authors SOPs and serves as a subject matter expert for the EDMS system.
Position Responsibilities
  • Evaluates data trends and authors reports associated with trends.
  • Leads and/or actively participates in investigations involving manufacturing process areas, related to QC processes or data, such as sampling, deviations potentially affecting QC results, investigational sampling, and testing.
  • Provides and follows up on ideas for continuous improvements in laboratory processes.
  • Maintains and troubleshoots testing equipment.
  • Completes required training and trains QC employees in GMP, SHE, QC methods and processes. As well as, good aseptic techniques, and instrumentation based on expertise.
  • Actively support and/or lead the implementation of compendial changes for raw materials, in-process or finished products tests in accordance with applicable Pharmacopoeias such as USP/NF, European Pharmacopeia, British, and Japanese Pharmacopeia.
  • Troubleshoots methods and processes.
  • May serve as an expert in a specific area of laboratory equipment, process, or system.
  • Serve as a subject manner expert during regulatory inspections including potential demonstrations and inspection room discussions.
  • Demonstrates expertise on authoring Quality records (Deviations, CAPAs, and Change Controls).
  • Answer and guide others in documentation, compliance, and other process questions.
  • Gather, organize, and communicate operational information to others.
  • Facilitate communication between management and non-management and team meetings.
  • Provide leadership, development, and mentoring for others.
  • Provide support in coordinating activities in the laboratory.
  • Identify temporary and permanent fixes to address issues.
  • Coordinate with representatives from other departments.
  • Attend team meetings to discuss progress, initiatives, and/or other matters.
  • Collect, record, report and trend metrics when applicable.
  • Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities.
  • Consult cross-functionally as an SME (Subject Matter Expert) on systems and/or processes within a functional area.
  • Perform logbook reviews.
  • Lead process improvement activities and teams to meet strategic goals.
  • Use MAXIMO and/or CMMS (Computerized Maintenance Management System) to manage logistics.
  • Alert supervisor or manager when problems occur outside of SOPs (Standard Operating Procedures).
  • Perform regular audits of SOPs (Standard Operating Procedures) and/or work instructions.
  • Review and approve documentation needed for qualification of equipment and processes.
  • Attend and facilitate inter-departmental meetings to discuss matters involving the coordination of multiple departments when necessary.
  • Interact with other departments to implement corrective/preventative actions.
  • Review and approve quality records as a SME when required.
  • Provide "off shift" support (i.e., night shift support if you normally workday shift).
  • Coordinate qualification activities.
  • Assess and implement improvements in productivity, waste generation, quality and cost.
  • Recommend compliance resolutions to management.

Hours (Day Shift):
  • Sunday - Wednesday
  • 10 hour shift

Minimum Qualifications
  • Prior experience in a regulated GMP environment.
  • Working knowledge of cGXP requirements and a strong familiarity with production operations.
  • Excellent attention to details and problem-solving skills.

Preferred Qualifications
  • Bachelor's degree in a Science subject (Microbiology, or closely related subjects)
  • 5 years QC Microbiology laboratory experience.
  • High level knowledge and competence with a specific piece of laboratory equipment, or a QC/QA process or system.
  • Prior experience supporting microbiological testing in a sterile pharmaceutical operation environment.

This position may also include the following conditions:
  • This role is primarily non-sedentary. May include but not limited to standing, walking, repetitive motion, and chemical usage.
  • All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role.
  • The items described here are representative of those that must be met successfully to perform the essential functions of this job.
  • The work schedule listed reflects the employee's expected schedule at the time of hire. The Company reserves the right to modify work schedules at any time, with or without notice, based on business needs, operational requirements, or other considerations. Nothing in this description creates a guarantee of specific hours, days, or shift assignments.

Sponsorship or support for work authorization, including visas, is not available for this position.
Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.
Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $75,000.00 - $116,250.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.

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