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Senior Qa Manager Jobs in Ohio (NOW HIRING)

Peak Nano

Quality Assurance Manager

Valley View, OH · On-site

$110 - $160/hr

... to senior leadership Preferred Qualifications Bachelor's degree in Engineering, Quality ... Assurance Management certification through ASQ or similar organization. About The Company Peak Nano ...

Confidential

Quality Assurance Manager

Cincinnati, OH · On-site

$110K - $125K/yr

Quality Assurance Manager - Northern Kentucky Do you enjoy leading quality, compliance, and food safety programs? Are you detail-oriented, proactive, and able to build strong relationships with ...

Sotera Health

Quality Assurance Manager

Marion, OH · On-site

The QA Manager maintains responsibility for all aspects connected with compliance, including the development, analysis and reporting of support data for regulatory agencies and Corporate Quality. In ...

Battelle

Quality Assurance Officer

Columbus, OH · On-site

$85K - $100K/yr

In collaboration with the Senior QA Officer and/or QA Manager, reviews research proposals to assess quality assurance requirements, ensuring regulatory requirements are adequately addressed and QA ...

Kutol-Product

Quality Assurance Manager

Cincinnati, OH · On-site

$110 - $140/hr

As the Quality Assurance Manager, you will lead QA activities for our OTC drug and cosmetic manufacturing operations, ensuring compliance with current Good Manufacturing Practices (cGMP), FDA ...

gaylor

Quality Assurance Manager

Hamlet, NC

The Quality Assurance Manager must be independent self-motivated, innovative, resourceful, and possess strong organizational and communication skills. The Quality Assurance Manager is pivotal in ...

Battelle

Quality Assurance Officer

Columbus, OH

$85K - $100K/yr

In collaboration with the Senior QA Officer and/or QA Manager, reviews research proposals to assess quality assurance requirements, ensuring regulatory requirements are adequately addressed and QA ...

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Senior Qa Manager information

See Ohio salary details

$27.1K

$92.3K

$173.5K

How much do senior qa manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for senior qa manager in Ohio is $92,313.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,600.00 and $129,800.00 per year, depending on experience, location, and employer.

What is a senior QA manager?

Senior QA Managers are experienced professionals responsible for overseeing quality assurance processes within an organization. They lead QA teams, develop testing strategies, ensure products meet quality standards, and collaborate with other departments to improve software or product reliability. Their role often involves mentoring junior QA staff, managing resources, and driving continuous improvement in testing methodologies. Senior QA Managers also play a key part in defining quality metrics and ensuring compliance with industry regulations.

How does a senior QA manager typically collaborate with cross-functional teams to ensure product quality?

A Senior QA Manager works closely with development, product management, and operations teams to align testing activities with business goals and release schedules. They facilitate regular meetings to discuss quality objectives, review test strategies, and coordinate bug tracking and resolution efforts. By fostering open communication and integrating QA processes into the overall development lifecycle, Senior QA Managers help ensure that quality is a shared responsibility and that potential issues are addressed early. This collaborative approach not only improves product outcomes but also enhances team efficiency and morale.

What are the key skills and qualifications needed to thrive as a senior QA manager, and why are they important?

To thrive as a Senior QA Manager, you need extensive experience in software quality assurance, deep knowledge of testing methodologies, and often a degree in computer science or a related field. Familiarity with automation tools (such as Selenium or JMeter), test management systems, and certifications like ISTQB are highly valued. Leadership, strategic thinking, and strong communication skills help manage teams and foster cross-functional collaboration. These capabilities ensure software quality, process efficiency, and seamless project delivery within complex development environments.

What are popular job titles related to Senior Qa Manager jobs in Ohio?

For Senior Qa Manager jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Senior Qa Manager jobs in Ohio look for?

The top searched job categories for Senior Qa Manager jobs in Ohio are:

What cities in Ohio are hiring for Senior Qa Manager jobs?

Cities in Ohio with the most Senior Qa Manager job openings:

Senior Qa Manager jobs near you
Infographic showing various Senior Qa Manager job openings in Ohio as of August 2026, with employment types broken down into 84% Full Time, 12% Part Time, 1% Temporary, and 3% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $92,313 per year, or $44.4 per hour.

Senior Quality Assurance Manager - BioScience

Smithfield Foods, Inc.

Cincinnati, OH • On-site

Full-time

Re-posted 23 days ago

Job description

If you are currently employed at Smithfield, please log into Workday and submit your application through the Jobs Hub.
Have a seat at our table. When you join Smithfield, you become part of something special - a company that's sustainably feeding people around the world, producing good food the right way with respect for our people, animals, communities and planet. With opportunities across locations and functions, a culture grounded in our Core Four values - gratitude, communication, respect and accountability - and a strong commitment to learning, collaboration, and innovation, Smithfield offers challenging and rewarding careers where you can grow, contribute and make a real impact. Apply Now!
THE VALUE YOU'LL BRING:
The position summary states the general nature and purpose of the job. Overall accountabilities are defined in this section.
Step Into a High-Impact Role in Quality Assurance!
Ready to make a real difference in the world of pharmaceutical and medical device manufacturing? Smithfield BioScience, Inc. (SBC) is seeking a quality-driven professional for a full-time role reporting to the Head of Quality-a position that sits at the heart of our mission to deliver products that meet the highest global standards.
As a Quality Assurance leader, you'll be on the front lines of enforcing current Good Manufacturing Practices (cGMP) and safeguarding the integrity of our quality management systems. You won't just be checking boxes-you'll be shaping the standards that ensure our FDA-registered facility operates with unmatched precision and compliance.
Your oversight will be critical to the manufacture of high-quality Active Pharmaceutical Ingredients (APIs) and medical device components, all in accordance with 21 CFR Parts 210/211, ICH Q7, ISO 22442, and EU regulatory guidelines. You'll own system controls, uphold procedural excellence, and be a key driver of continuous improvement and operational readiness.
If you're passionate about compliance, thrive in a fast-paced regulated environment, and are ready to lead with confidence-this is the opportunity for you.
WHAT YOU'LL DO:
The below statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. May perform other duties as assigned.
Quality Assurance Leadership
  • Lead and manage the QA team to ensure full compliance with cGMP standards and adherence to internal SOPs.
  • Provide strategic direction and decision-making on all quality-related matters, acting as a go-to leader during escalations.
  • Champion a culture of quality-first thinking, driving operational excellence across departments.

Process Development & Continuous Improvement
  • Collaborate in the design, development, and refinement of quality systems, procedures, and product processes.
  • Drive continuous improvement initiatives across QA operations to streamline workflows and elevate product quality.
  • Coordinate with Regulatory Affairs to assess the impact of critical change control activities on customer satisfaction and compliance.

Data Management & Reporting
  • Ensure accurate recordkeeping, archival, and retrieval of all QA-related data, supporting traceability and audit-readiness.
  • Compile and present quality metrics and key performance indicators (KPIs) to senior management for informed decision-making.
  • Assist in preparation and presentation of the Annual Product Review to the Quality Review Board.

Regulatory Compliance & Inspection Readiness
  • Maintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections.
  • Actively participate in internal audits, customer audits, and regulatory inspections, demonstrating a deep understanding of applicable standards.
  • Stay current with evolving FDA, EU, and ICH regulations, ensuring company procedures remain aligned with global expectations.

Quality Systems Oversight
  • Oversee and safeguard company Quality Management System (QMS) records to ensure accuracy, security, and compliance.
  • Ensure timely and thorough investigations of OOS (Out of Specification) results, CAPAs, complaints, and deviations, all in accordance with FDA guidelines.
  • Collaborate cross-functionally to support the validation of company processes, test methods, and computerized systems.

Skills & Competencies
  • Detail-Oriented Problem Solver - Able to spot quality issues early and implement smart, sustainable solutions.
  • Exceptional Communicator - Strong written and verbal communication skills, essential for audits, reporting, and cross-team collaboration.
  • QMS & Tech Proficiency - Experience with digital quality systems like TrackWise Digital or similar platforms.
  • Team Player with Leadership Drive - Comfortable managing multiple priorities in a collaborative, fast-paced environment.
  • Analytical Thinker - Brings logic, critical thinking, and data-driven decision-making to every challenge.

WHAT WE'RE SEEKING:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions.
  • Bachelor's degree from an accredited four-year college or university in a chemistry, microbiology or other relevant technical field and 8+ years of relevant manufacturing experience, or an equivalent combination of education and experience, required.
  • Minimum 2 years of demonstrated experience in team management/development or project leadership is required preferably in pharmaceutical cGMP manufacturing.
  • Candidates with a Master's Degree in a Science or Technical field from an accredited four-year college or university and 6+ years relevant experience will be considered qualified.
  • In-depth knowledge of relevant regulations and standards in the pharmaceutical industry (e.g., 21 CFR Part 210/211, ICH Q7, 21 CFR Part 11).
  • Strong understanding of Good Manufacturing Practices (GMP) and their application in the pharmaceutical industry.
  • Experience in developing, implementing, and maintaining a quality management system.
  • Experience in conducting internal and external audits and managing audit programs.
  • Proficient with the TrackWise QMS modules for Quality Events, CAPA, OOS, and Audit (or equivalent eQMS system).
  • Familiarity with risk management principles and tools, including FMEA (Failure Modes and Effects Analysis) and risk assessment methodologies.
  • Excellent analytical, problem-solving, and root cause analysis skills, with the ability to apply data-driven decision-making.
  • Strong written and verbal communication skills, with the ability to effectively interact with cross-functional teams, regulatory authorities, and external stakeholders.
  • Relevant certifications such as Certified Quality Manager (CQM), Certified Quality Auditor (CQA), or Six Sigma Black Belt are advantageous
  • Strong Communicator: Exceptional written and verbal communication skills, capable of articulating complex technical issues clearly and concisely across all levels of the organization. Bilingual communication in Mandarin and English is preferred.

IndSPR-Ops
The expected pay range for this position is $120,000 - $162,500 annually.
Smithfield Foods provides pay ranges that reflect its good faith estimate of the salary or hourly wage the company reasonably expects to pay for a position at the time of hire. Individual compensation will be determined based on several factors, including but not limited to, the scope and responsibilities of the role, location of the position, the candidate's qualifications and experience, internal equity, external market pay for comparable positions and budget considerations. At Smithfield Foods, base pay represents only one aspect of the comprehensive total rewards package. Learn more about our benefits package here.
Relocation Package AvailableYes
EEO Information
Smithfield is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, gender identity, protected veterans status, status as a disabled individual or any other protected group status or non-job characteristic as directed by law.
If you are an individual with a disability and would like to request a reasonable accommodation for any part of the employment selection process, please call us at 757-357-1595.

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