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Quality Control Associate Jobs in Manning, SC (NOW HIRING)

Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory ... Systems Associate; including direction, assignment of work, hiring, development and training ...

Our focus has always been bringing our customers a constant stream of high-quality brands and on ... Responsible for security of building including entrance/exit control (Associate entry/egress ...

Our focus has always been bringing our customers a constant stream of high-quality brands and on ... Responsible for security of building including entrance/exit control (Associate entry/egress ...

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Quality Control Associate information

See Manning, SC salary details

$10

$23

$35

How much do quality control associate jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for quality control associate in Manning, SC is $23.66, according to ZipRecruiter salary data. Most workers in this role earn between $17.21 and $28.80 per hour, depending on experience, location, and employer.

What is a QC Associate job description?

A Quality Control (QC) Associate is responsible for inspecting and testing products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to address issues, often using tools like measurement instruments and quality management systems. The role typically requires attention to detail, knowledge of quality procedures, and adherence to safety protocols.

What does a Quality Control Associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

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

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges Quality Control Associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

Which pays more, QA or QC?

Quality Assurance (QA) and Quality Control (QC) roles often have similar pay scales, but QA positions typically offer higher salaries due to their focus on process improvement and prevention. Factors such as industry, experience, certifications, and location can influence compensation for both roles.

What do quality control associates do?

Quality control associates inspect products, materials, or processes to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or production environments to identify defects and ensure product consistency.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

Is QC a high paying job?

The salary for a Quality Control Associate varies depending on industry, experience, and location, but it is generally considered an entry-level to mid-level position with moderate pay. Higher salaries are often associated with advanced certifications, specialized skills, or supervisory roles within quality control departments.
What cities near Manning, SC are hiring for Quality Control Associate jobs? Cities near Manning, SC with the most Quality Control Associate job openings:
Infographic showing various Quality Control Associate job openings in Manning, SC as of July 2026, with employment types broken down into 1% As Needed, 57% Full Time, 40% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $49,222 per year, or $23.7 per hour.
Associate Quality Director

Associate Quality Director

Becton, Dickinson and Company

Sumter, SC • On-site

Full-time

Re-posted 6 days ago


BD rating

7.3

Company rating: 7.3 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

265th of 430 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

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Primary Work LocationUSA SC - SumterAdditional LocationsWork Shift

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About BD

Sourced by ZipRecruiter

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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