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Manager Qc Jobs in Springboro, OH (NOW HIRING)

RESILIENCE

Analyst II, QC Microbiology

West Chester, OH · On-site

$22.75 - $30.50/hr

For more information, please visit www.resilience.com Position Summary The Analyst II, QC ... Alert supervisor or manager when problems occur outside of SOPs (Standard Operating Procedures)

ALPLA Group

Quality Manager

Vandalia, OH · On-site

Oversite responsibility for plant quality control program including test equipment operation/calibration/verification, product testing, data collection, data integrity and rework management.

Mane USA

QC Lab Tech - Weekend Shift Nights

Lebanon, OH · On-site

$18 - $22.75/hr

The main duty of the Quality Control Lab Technician I/II is to inspect finished goods, work in ... Other duties as assigned by management * Consistent with MANE's environmental commitments ...

STEM Talent Solutions

Be Seen First

Quality Manager

Dayton, OH · On-site

$95K - $120K/yr

Quality Manager Seeking an experienced Quality Manager to lead Quality Assurance, Quality Control, Supplier Quality, and the Quality Management System (QMS) in a manufacturing environment.

gaylor

Quality Assurance Manager

Trenton, OH · On-site

The ideal candidate can establish and maintain quality control goals through training to ensure ... The Quality Assurance Manager is pivotal in electrical installations to ensure the highest ...

Glanbia

Quality Technician I

Sharonville, OH

$18 - $23/hr

Quality Control Related Responsibilities * Implement various analytical tests on incoming samples ... Communicate issues to Quality and/or Production Management, take ownership of solving batch ...

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Showing results 21-40

All JobsQc JobsManager Qc JobsManager Qc Jobs in Springboro, OH

Manager Qc information

See Springboro, OH salary details

$21.2K

$76K

$139.3K

How much do manager qc jobs pay per year?

As of Aug 21, 2026, the average yearly pay for manager qc in Springboro, OH is $75,968.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,800.00 and $119,900.00 per year, depending on experience, location, and employer.

What are the responsibilities of a Manager QC?

A Manager QC (Quality Control Manager) is responsible for overseeing the quality assurance processes within a company to ensure that products meet required standards and specifications. They develop and implement quality control procedures, supervise QC staff, conduct audits, and analyze quality data to identify areas for improvement. Additionally, they collaborate with other departments to resolve quality issues and ensure compliance with industry regulations. Their ultimate goal is to maintain consistent product quality and customer satisfaction.

What skills and qualifications are needed to thrive as a Manager QC?

To thrive as a Manager QC (Quality Control), you need a solid background in quality assurance processes, analytical testing, and industry regulations, typically supported by a degree in science or engineering. Familiarity with quality management systems (like ISO standards), statistical analysis software, and certification such as Six Sigma or ASQ is often required. Strong leadership, problem-solving, and communication skills help drive team performance and handle complex quality issues. These skills are essential for maintaining product standards, ensuring regulatory compliance, and supporting continuous improvement within the organization.

What challenges does a Manager QC face when balancing regulatory compliance with production timelines?

A Manager QC (Quality Control) often faces the challenge of ensuring that all products meet strict regulatory standards while also supporting the company's production goals. This balancing act requires effective communication with production and regulatory teams, as well as proactive planning to anticipate potential bottlenecks. Managers must remain vigilant about documentation and testing, and be prepared to address unforeseen quality issues without causing significant delays. Success hinges on strong leadership, a detail-oriented mindset, and the ability to adapt quickly to changing priorities.

What is the difference between Manager Qc vs Quality Assurance Supervisor?

AspectManager QcQuality Assurance Supervisor
ResponsibilitiesOversees quality control processes, manages teams, implements quality policiesSupervises QA team, conducts inspections, ensures compliance with standards
CredentialsBachelor's degree in related field, experience in quality management, certifications like CQEBachelor's degree, experience in quality assurance, certifications like CQE or ASQ certifications
Work EnvironmentManagement level, strategic planning, cross-department collaborationOperational level, hands-on inspections, team supervision
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, electronics, consumer goods

The main difference between a Manager Qc and a Quality Assurance Supervisor lies in scope and level of responsibility. The Manager Qc typically handles strategic oversight and manages multiple teams, while the QA Supervisor focuses on daily supervision and operational tasks. Both roles require similar credentials and are vital in quality management across industries.

Is manager QC a high paying job?

Manager QC roles typically offer higher salaries compared to entry-level quality control positions, with pay varying based on industry, experience, and location. These roles often require strong leadership, technical skills, and certifications, and they tend to be well-compensated in manufacturing, pharmaceuticals, and food industries.

What does a manager QC do?

A manager QC (Quality Control) oversees the inspection and testing of products or processes to ensure they meet quality standards. They develop quality procedures, supervise QC staff, analyze data, and implement improvements to maintain product integrity and compliance with industry regulations.

What cities near Springboro, OH are hiring for Manager Qc jobs?

Cities near Springboro, OH with the most Manager Qc job openings:

Manager Qc jobs near you
Infographic showing various Manager Qc job openings in Springboro, OH as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 13% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $75,968 per year, or $36.5 per hour.

Analyst II, QC Microbiology

RESILIENCE

West Chester, OH • On-site

$22.75 - $30.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 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 Analyst II, QC Microbiology role supports the Microbiology Department by performing quality-related tasks for pharmaceutical products to include documenting and conducting testing on a variety of samples, such as raw materials, in-process and finished products, stability samples, water, gas, and environmental samples.
Job Responsibilities
  • Read SOPs (Standard Operating Procedures) and excerpts from technical documentation.
  • Write, review, and revise SOPs (Standard Operating Procedures) and/or work instructions for cGMP (Good Manufacturing Practices) manufacturing of commercial product.
  • Complete required training and may train others.
  • Conduct troubleshooting activities.
  • Gather, organize, and communicate operational information to others.
  • Facilitate team meetings to discuss progress, initiatives, and/or other matters.
  • 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.
  • Assist with coordinating activities of support groups.
  • Identifies trends in data in order to provide accurate descriptions, identify root causes, and/or identify solutions or improvements.
  • Demonstrates proficiency on authoring Quality records (Deviations, CAPAs, and Change Controls).
  • Identify temporary and permanent fixes to address issues.
  • Alert supervisor or manager when problems occur outside of SOPs (Standard Operating Procedures).
  • Collect, record, and report metrics.
  • Monitor equipment and/or systems for performance and problem indicators.
  • 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 or participate in process improvement activities and teams to meet strategic goals.
  • Use MAXIMO and/or CMMS (Computerized Maintenance Management System) to manage logistics.
  • Interact with regulatory agency individuals during audits and inspections, when necessary.
  • Author, review, and revise documentation needed for cGMP (Good Manufacturing Practices) manufacturing of commercial product.
  • Attend inter-departmental meetings to discuss matters involving the coordination of multiple departments.
  • Coordinate qualification activities.
  • Perform routine sampling activities on the facility utilities.
  • Recommend compliance resolutions to management.

Minimum Qualifications
  • Working knowledge of cGXP requirements and a strong familiarity with production operations.
  • Good problem solving skills.

Preferred Qualifications
  • Bachelor's degree in biology, microbiology, or related discipline.
  • At least 2 year of laboratory experience in pharmaceutical industry.
  • 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.
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 $60,000.00 - $86,250.00 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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