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Entrylevel Quality Control Inspector Jobs in Concord, NC

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

... Inspections, well acquainted with QMS, well versed with Change control/deviations and market ... Support the Management to organize and maintain the QC team, good communications skills, front ...

The Bradley Group

Be Seen First

Quality Control Associate

Charlotte, NC · On-site

$22/hr

... Control Associate to join our growing team in Monroe, NC. This is a hands-on position --you'll ... Inspect incoming products for color, texture, and overall quality. * Verify SKUs, labels, and box ...

Commercial Metals Company

QC Technician

Denver, NC · On-site

$17.25 - $22.25/hr

Perform quality control tests on raw materials, in-process, and finished products ... Inspect products for defects, dimensional accuracy, and adherence to specifications. * Document and ...

SLR Search

Quality Inspector

Charlotte, NC

$20 - $23/hr

Exciting opportunity for a Quality Inspector looking to grow within a stable organization. Quality ... quality control and use of measurement tools. -- Perform quality checks on production output ...

Commercial Metals Company

QC Technician

Denver, NC · On-site

$17.25 - $22.25/hr

Perform quality control tests on raw materials, in-process, and finished products ... Inspect products for defects, dimensional accuracy, and adherence to specifications. * Document and ...

Industrial Fabricators

Quality Inspector

Gastonia, NC

$20 - $28/hr

Quality InspectorPosition Summary IFAB Corp is seeking a Quality Inspector to support quality control for metal fabricated automotive components across our manufacturing operations, including heavy ...

E2 Optics

QA/QC Coordinator

Charlotte, NC

$19.25 - $26.50/hr

Join Our Team as a QA/QC Coordinator at E2 Optics! Are you ready to elevate your career with an ... Inspections & Reporting: Conduct quality inspections, generate data analytics, and track ...

RK&K

Inspector

Charlotte, NC · On-site

As a construction inspector in RK&K's Construction/CEI division you will perform complex and ... Inspects work zones for proper traffic control setup, erosion control devices and maintenance ...

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All JobsEntrylevel Quality Control Inspector JobsEntrylevel Quality Control Inspector Jobs in Concord, NC

Entrylevel Quality Control Inspector information

See Concord, NC salary details

$10

$20

$31

How much do entrylevel quality control inspector jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for entrylevel quality control inspector in Concord, NC is $20.00, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $22.40 per hour, depending on experience, location, and employer.
What are popular job titles related to Entrylevel Quality Control Inspector jobs in Concord, NC? For Entrylevel Quality Control Inspector jobs in Concord, NC, the most frequently searched job titles are:
What job categories do people searching Entrylevel Quality Control Inspector jobs in Concord, NC look for? The top searched job categories for Entrylevel Quality Control Inspector jobs in Concord, NC are:
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Entrylevel Quality Control Inspector jobs near you
Infographic showing various Entrylevel Quality Control Inspector job openings in Concord, NC as of July 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $41,603 per year, or $20 per hour.

Quality Control Analyst

Glenmark Pharmaceuticals

Monroe, NC • On-site

$22.25 - $30/hr

Full-time

Posted 17 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.

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