ZipRecruiter

Log In

1

Quality Control Assistant Jobs in Lancaster, SC (NOW HIRING)

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Execute cleaning validation of new products. * Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab.

ProSidian Consulting

Quality Control Analyst

Charlotte, NC · On-site

$22.50 - $30/hr

Additionally, the Quality Control Analyst will assist and monitor the Curriculum Developer in collecting data via surveys and focus groups to assess the effectiveness of training sessions and ...

Heidelbergmaterials

QC Tech

Mcconnells, SC · On-site

$25 - $29.32/hr

Aggregates QC Technician About Us Heidelberg Materials is one of the world's largest suppliers of ... quality concerns and recommending corrective actions. * Assist with customer support ...

New

Huntsman

QC Lab Chemist

Rock Hill, SC · On-site

Troubleshoot QC laboratory instrumentation and assist with maintaining analytical equipment performance. * Utilize laboratory software and instrumentation systems to collect, review, and interpret ...

Huntsman Corporation

QC Lab Chemist

Rock Hill, SC · On-site

Troubleshoot QC laboratory instrumentation and assist with maintaining analytical equipment performance. * Utilize laboratory software and instrumentation systems to collect, review, and interpret ...

Riley Power Group

Sr. Manager, QC

Rock Hill, SC · On-site

Essential Duties & Responsibilities Quality Control Management * Manage and maintain company ... * Assist in resolving welding-related production, fabrication, and field issues. * Review ...

InChem

QC Lab Chemist 3rd Shift (Aug '26)

Rock Hill, SC · On-site

QC Lab Chemist - 3rd shift Classification: Hourly Non-Exempt Reports to: QC Lab Manager Summary ... Maintain laboratory organization and cleanliness in accordance with 5S principles. * Assist with ...

New

InChem

QC Lab Chemist 3rd Shift (Aug '26)

Rock Hill, SC · On-site

QC Lab Chemist - 3rd shift Classification: Hourly Non-Exempt Reports to: QC Lab Manager Summary ... Maintain laboratory organization and cleanliness in accordance with 5S principles. * Assist with ...

New

next page

Showing results 1-20

All JobsQuality Control JobsQuality Control Assistant JobsQuality Control Assistant Jobs in Lancaster, SC

Quality Control Assistant information

See Lancaster, SC salary details

$10

$19

$34

How much do quality control assistant jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for quality control assistant in Lancaster, SC is $19.48, according to ZipRecruiter salary data. Most workers in this role earn between $13.94 and $19.66 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality control assistant, and why are they important?

To thrive as a Quality Control Assistant, you need strong attention to detail, basic understanding of quality assurance principles, and at least a high school diploma or equivalent. Familiarity with industry-specific inspection tools, measurement instruments, and software such as Microsoft Excel or specialized quality management systems is often required. Excellent organizational skills, effective communication, and the ability to work both independently and collaboratively set top performers apart. These skills are crucial for ensuring products consistently meet quality standards and for supporting efficient production processes.

What do quality control assistants do?

Quality control assistants inspect products, materials, or processes to ensure they meet quality standards and specifications. They often use testing tools, follow detailed procedures, and document findings to help maintain product consistency and safety in manufacturing or production environments.

What is a quality control assistant?

Quality Control Assistants are professionals who help ensure that products or services meet established quality standards. They assist in inspecting, testing, and evaluating materials or products during various stages of production. Their responsibilities often include recording data, reporting defects, and supporting the implementation of quality assurance procedures. By maintaining high quality standards, they help companies reduce errors, improve customer satisfaction, and comply with industry regulations.

What are some common challenges quality control assistants face when ensuring product consistency, and how can they overcome them?

Quality Control Assistants often encounter challenges such as identifying subtle defects in products, maintaining accurate records under time pressure, and effectively communicating quality issues to production teams. Overcoming these challenges requires keen attention to detail, strong organizational skills, and the ability to collaborate with colleagues from different departments. Regular training on inspection standards and open communication with supervisors can help QC Assistants stay updated and maintain high-quality results.

What is the difference between Quality Control Assistant vs Quality Inspector?

AspectQuality Control AssistantQuality Inspector
CertificationsBasic quality assurance training, sometimes certifications like Six Sigma or ISO awarenessMore advanced certifications often preferred, such as Certified Quality Inspector (CQI)
Work EnvironmentAssist in quality checks, support documentation, and process monitoring in manufacturing or production settingsConducts detailed inspections, tests products, and ensures compliance with standards on the production line
Employer & Industry UsageUsed across manufacturing, food production, and assembly industries as entry-level or support roleCommonly employed in manufacturing, aerospace, automotive, and electronics industries for quality assurance

While both roles focus on quality assurance, the Quality Control Assistant typically supports inspection processes and documentation, whereas the Quality Inspector performs detailed product inspections and testing. The roles often overlap, but the inspector usually has more specialized training and responsibilities.

More about Quality Control Assistant jobs
What are the most commonly searched types of Quality Control jobs in Lancaster, SC? The most popular types of Quality Control jobs in Lancaster, SC are:
What are popular job titles related to Quality Control Assistant jobs in Lancaster, SC? For Quality Control Assistant jobs in Lancaster, SC, the most frequently searched job titles are:
What cities near Lancaster, SC are hiring for Quality Control Assistant jobs? Cities near Lancaster, SC with the most Quality Control Assistant job openings:
Quality Control Assistant jobs near you
Infographic showing various Quality Control Assistant job openings in Lancaster, SC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $40,511 per year, or $19.5 per hour.

Quality Control Analyst

Glenmark Pharmaceuticals

Monroe, NC • On-site

$22.25 - $30/hr

Full-time

Re-posted 13 days ago

Job description

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules - both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets APIs to regulated and semi-regulated countries.
POSITION SUMMARY:
This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide information, data for evaluation and execution of stability study as per Quality and regulatory requirement. Timely complete testing and ensure compliance during analytical TT and AMV performed in QC lab. Able to be a qualified trainer for QC related systems and SOP's and responsible that personnel are appropriately trained.
OVERALL JOB RESPONSIBILITIES:
  • Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project.
  • Provide feedback to management with laboratory standard hours for financial prudence in resource planning, allocation and manpower to ensure within approved budgets while building best in class quality processes and systems at site.
  • Execute and maintain quality system controls to ensure no critical and major market complaints.
  • Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency
  • Perform day to day activities for the chemical laboratory which shall include testing of in- process, RM, PM and FP samples, Swab sample and Tech Transfer (as applicable).
  • Ensuring compliance to systems and procedures throughout product lifecycle.
  • Communicate with Supervisor and/or report any preparations or data that may result in an Incidence & OOS.
  • Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits.
  • Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products.
  • Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab.
  • Apply CAPA for Lab failures in OOS.
  • Prepare in timely fashion updating and revision of SOP, specification, STP and any other documents
  • Assist in timely completion of Tech Transfer of Finished products.
  • Ensure training of QC staff
  • Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc.
  • Perform the Training Tracking Tool/Software for QUALITY Assurance and Quality Control.

Education :
B.Sc. in Chemistry with concentration in Biochemistry
Experience:
• 1-3 years in the field of Pharmaceutical (manufacturing facility).
• Background in the functional areas of Quality Control in Stability, Finished Goods and some Raw Materials with a some experience in R&D.
Extensive knowledge in general laboratory equipment including but not limited to: HPLC, UV-Vis and FTIR.
Knowledge and Skills :
Knowledge of cGMP, Validations and Qualifications, regulatory guidelines, US Pharmacopoeias, Internal auditing, Handling of regulatory Inspections, well acquainted with QMS, well versed with Change control/deviations and market compliant management system.
Skills in coordination of calibration and preventative maintenance services, including but not limited to: setting up vendor contracts, processing quotes, generating purchasing orders and handling vendor invoices.
Technical writing skills to generate SOPs and serve as the Subject Matter Expert.
Began training under Six Sigma and Project Management.
Support the Management to organize and maintain the QC team, good communications skills, front runner, and GMP trainer.
Other requirements (licenses, certifications, specialized training)
Will be an added advantage if the individual has dealt with multiple audits personally.

Apply