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Software Quality Operations Associate Jobs in Columbia, SC

... and quality of work produced. Responsible for motivating associates to meet individual and ... Required Software and Tools: Microsoft Office. We Prefer That You Have the Following: * Preferred ...

... and quality of work produced. Responsible for motivating associates to meet individual and ... Required Software and Tools: Microsoft Office. We Prefer That You Have the Following: * Preferred ...

Quality - Testing

Camden, SC · On-site

$14.75 - $19.75/hr

In this role you must be able to support associates and supplement the group's labor force as ... Must be able to read Calipers, Micrometers and Prints * 1 year experience with Microsoft Software ...

Quality - Testing

Camden, SC · On-site

$14.75 - $19.75/hr

In this role you must be able to support associates and supplement the group's labor force as ... Quality Equipment Operation. Assist in creation of MCPs and MCIs and that these are included in ...

Analyze and test software to ensure that products meet design specifications and are within total ... Deep knowledge of healthcare operations (preferably Medicaid), business processes Proficient in ...

Quality Engineer

Columbia, SC

$66K - $86K/yr

... to verify operational and performance parameters * Evaluate engineering change orders and ... Support software validations, maintenance activities, and requalification efforts * Develop product ...

... quality operations. You will work closely with engineers and production teams to ensure parts and ... Exposure to metrology software such asPolyWorks, ZEISS INSPECT, or similar applications.

Showing results 41-60

Software Quality Operations Associate information

See Columbia, SC salary details

$10

$24

$46

How much do software quality operations associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for software quality operations associate in Columbia, SC is $24.92, according to ZipRecruiter salary data. Most workers in this role earn between $16.92 and $29.13 per hour, depending on experience, location, and employer.

What is a software quality operations associate?

A Software Quality Operations Associate is a professional who supports the quality assurance (QA) processes within a software development organization. Their main responsibilities include monitoring software quality, helping to implement QA procedures, coordinating testing activities, and ensuring that software products meet established standards before release. They often work closely with QA engineers, developers, and product managers to track defects, document issues, and improve workflow efficiency. This role is essential for maintaining high software quality and facilitating smooth operations within the QA team.

What are the key skills and qualifications needed to thrive as a software quality operations associate, and why are they important?

To thrive as a Software Quality Operations Associate, you need a solid understanding of software development processes, quality assurance principles, and a relevant degree in computer science or a related field. Familiarity with test management tools (like JIRA or TestRail), bug tracking systems, and automation frameworks is typically required, along with any relevant QA certifications. Strong analytical thinking, attention to detail, and effective communication skills help you excel in identifying issues and collaborating with development teams. These skills ensure the delivery of high-quality software products and support efficient, error-free operations.

What is the difference between Software Quality Operations Associate vs Software Quality Analyst?

AspectSoftware Quality Operations AssociateSoftware Quality Analyst
CredentialsTypically requires a bachelor's degree in computer science, quality assurance, or related fieldUsually requires a bachelor's degree in computer science, software engineering, or related discipline
Work EnvironmentWorks within software development teams, focusing on process and operationsFocuses on testing, identifying bugs, and analyzing software quality
Employer & Industry UsageCommon in tech companies, software firms, and IT departmentsWidely used in software development, IT, and quality assurance sectors

The Software Quality Operations Associate primarily handles quality processes and operational tasks within software teams, while the Software Quality Analyst concentrates on testing and analyzing software quality. Both roles require similar educational backgrounds and are integral to software development, but they focus on different aspects of quality assurance.

What are some of the typical challenges faced by a software quality operations associate when coordinating between development and QA teams?

One of the main challenges for a Software Quality Operations Associate is ensuring clear and timely communication between development and QA teams, especially when managing tight release schedules. Balancing the need for rapid deployment with thorough testing can create pressure to prioritize tasks and manage resources efficiently. Additionally, adapting to shifting project requirements and quickly resolving bugs or discrepancies requires strong organizational and problem-solving skills. Proactively fostering collaboration and maintaining detailed documentation help overcome these obstacles and contribute to smoother software delivery.

What are popular job titles related to Software Quality Operations Associate jobs in Columbia, SC?

For Software Quality Operations Associate jobs in Columbia, SC, the most frequently searched job titles are:

What job categories do people searching Software Quality Operations Associate jobs in Columbia, SC look for?

The top searched job categories for Software Quality Operations Associate jobs in Columbia, SC are:

Infographic showing various Software Quality Operations Associate job openings in Columbia, SC as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $51,825 per year, or $24.9 per hour.

Associate Quality Director

Becton, Dickinson and Company

Sumter, SC • On-site

Full-time

Re-posted 8 days ago


BD rating

7.3

Company rating: 7.3 out of 10

Based on 140 frontline employees who took The Breakroom Quiz

309th of 490 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Reporting to the VP of Quality Management, the Associate Director, Plant QA leads and directly manages technical and managerial staff at the Sumter facility. This role plays a pivotal part in shaping global quality strategy and driving the tactical execution needed to achieve organizational objectives.
Through exceptional communication, proactive problem-solving, and confident navigation of ambiguity, the Associate Director ensures product safety, quality, and full compliance with global regulations and customer expectations.
Success in this role is measured by the minimization of product quality and organizational issues, as well as the continuous improvement of business process effectiveness. By fostering strong relationships with internal and external stakeholders - and investing in the growth and development of people - the Associate Director, Plant QA delivers sustainable, industry-leading results that support key business drivers.
Responsibilities:
As the Management Representative for the Sumter Plant, (as defined per ISO 13485:2003 and 21 CFR 820). you'll serve as the cornerstone of our quality management system, bringing quality standards to life through:
  • Quality System Champion - Establishing, implementing, and maintaining vital quality management processes
  • Executive Quality Liaison - Delivering insightful performance reports to top management through Management Review meetings, highlighting improvement opportunities
  • Regulatory Awareness Ambassador - Fostering a culture where every team member understands and embraces regulatory and customer requirements
  • Inspection Point Person - Serving as the primary contact for FDA, ISO, and third-party audits, representing the Sumter site
  • Compliance Program Overseer - Managing comprehensive quality activities including CAPA, Quality Notifications, Temporary Deviations, Internal and Supplier Audits, Change Control, Calibration, and Complaint Investigations.
    • This includes compliance to applicable regulations and standards for medical devices and pharmaceutical products.
  • Product Release Guardian - Supervising laboratory operations and release personnel to ensure only safe, effective products reach customers, including on-site sterilization quality oversight
    • Responsible for approval or rejection of components, finished products, and documents to achieve this purpose.
  • Strategic Leadership Team Member - Contributing to the Plant Leadership Team and Executive Steering Committee to drive plant initiatives and achieve organizational goals
  • Quality Strategy Architect - Developing and maintaining forward-thinking quality plans and policies that align business objectives with regulatory requirements
  • Continuous Improvement Driver - Directing Quality Assurance projects through leadership teams to maintain regulatory compliance and support plant continuous improvement efforts
  • Talent Developer - Building a high-performing quality team through targeted training and professional development opportunities
  • Financial Steward - Managing the Quality department and laboratory budget with efficiency and foresight
  • Problem-Solving Partner - Collaborating with multi-functional teams to identify root causes of quality issues and customer complaints. Works with the Design Center Quality Management to drive investigations for product issues in the field and assists with the preparation of Situation Analyses.
  • Product Development Collaborator - Supporting new product initiatives and facilitating smooth Design Transfer from development to manufacturing
  • Safety Compliance Advocate - Adhering to all local, state, federal, and BD safety regulations, including RCRA Hazardous waste protocols

Required Qualifications:
  • BS degree in Engineering or Life Sciences
  • 5 years Managerial experience in highly regulated Medical Device Plant

Preferred Qualifications:
  • Master Degree in Business or Engineering
  • ASQ Certification
  • Six Sigma Certification

Knowledge and Skills:
  • Exhibits an exceptional degree of ingenuity, creativity, and resourcefulness
  • Applies and / or develops highly advanced technologies, scientific principles, theories and concepts.(Viewed as expert within the field)
  • Provides technical knowledge and expertise related to competitive products as well as process technologies not currently employed at BD
  • Acquires and adapts new techniques and technologies
  • ISO 13485, 21 CFR 820, and MDSAP regulatory and quality system knowledge

Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
Primary Work Location
USA SC - Sumter
Additional Locations
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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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