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Quality Control Lab Manager Jobs in Monroe, NC (NOW HIRING)

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

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 ...

Huntsman

QC Lab Chemist

Rock Hill, SC

This position will report to the Quality Manager . Job Scope The QC Laboratory Chemist is responsible for performing Quality Control testing on raw materials, in-process materials, and finished ...

NOVA Engineering

Lab Manager (CMT/Soils)

Charlotte, NC · On-site

Performing specific QA/QC tests on construction materials and building components such as soil ... Manage lab personnel and maintain required certifications among the laboratory team. * Maintaining ...

Huntsman Corporation

QC Lab Chemist

Rock Hill, SC · On-site

This position will report to the Quality Manager . Job Scope The QC Laboratory Chemist is responsible for performing Quality Control testing on raw materials, in-process materials, and finished ...

NOVA Engineering

Lab Manager (CMT/Soils)

Charlotte, NC · On-site

Performing specific QA/QC tests on construction materials and building components such as soil ... Manage lab personnel and maintain required certifications among the laboratory team. * Maintaining ...

TransTech Group

Quality Control Manager

Charlotte, NC · On-site

Quality Control Manager Location: Charlotte, NC Company Overview Bendel Tank and Heat Exchanger, LLC, a division of TransTech Group, LLC, is a leading manufacturer of custom Carbon Steel, Stainless ...

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All JobsQuality Control Lab JobsQuality Control Lab Manager JobsQuality Control Lab Manager Jobs in Monroe, NC

Quality Control Lab Manager information

See Monroe, NC salary details

$28.3K

$75.4K

$120.1K

How much do quality control lab manager jobs pay per year?

As of Jul 26, 2026, the average yearly pay for quality control lab manager in Monroe, NC is $75,396.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,100.00 and $92,700.00 per year, depending on experience, location, and employer.

What does a Quality Control Lab Manager do?

A Quality Control Lab Manager oversees the daily operations of a laboratory to ensure that products meet industry and safety standards. They supervise lab staff, develop testing protocols, review test results, and maintain compliance with regulatory guidelines. The manager is also responsible for training employees, troubleshooting equipment, and implementing improvements to lab processes. Their work is crucial in guaranteeing the quality and safety of products before they reach consumers.

What is the difference between Quality Control Lab Manager vs Quality Control Technician?

AspectQuality Control Lab ManagerQuality Control Technician
CredentialsBachelor's degree in science or related field; often certifications in quality managementAssociate's or bachelor's degree; relevant technical certifications
Work EnvironmentLaboratories, overseeing testing processes and staffLaboratories, performing tests and data collection
ResponsibilitiesSupervising testing activities, managing staff, ensuring complianceConducting tests, recording results, maintaining equipment

The main difference between a Quality Control Lab Manager and a Quality Control Technician lies in their responsibilities and level of oversight. The manager oversees testing operations, manages staff, and ensures quality standards, while the technician performs the actual testing and data collection. Both roles require relevant scientific credentials and work in laboratory environments, but the manager holds a broader supervisory role.

What are some common challenges faced by a Quality Control Lab Manager, and how can they be addressed?

Quality Control Lab Managers often face challenges such as ensuring compliance with evolving regulatory standards, maintaining the accuracy and reliability of test results, and managing a diverse team of technicians. To address these issues, managers must stay updated on industry regulations, implement rigorous training programs, and foster open communication within the team. Effective use of laboratory information management systems (LIMS) and regular audits can also help maintain high-quality standards and streamline workflows.

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

To thrive as a Quality Control Lab Manager, you need a solid background in chemistry or biology, experience in laboratory operations, and often a relevant degree or certification. Familiarity with laboratory information management systems (LIMS), analytical instrumentation, and quality standards such as ISO or GMP is typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring compliance. These skills and qualities are crucial to maintain product quality, regulatory adherence, and efficient laboratory performance.
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What job categories do people searching Quality Control Lab Manager jobs in Monroe, NC look for? The top searched job categories for Quality Control Lab Manager jobs in Monroe, NC are:
What cities near Monroe, NC are hiring for Quality Control Lab Manager jobs? Cities near Monroe, NC with the most Quality Control Lab Manager job openings:
Quality Control Lab Manager jobs near you
Infographic showing various Quality Control Lab Manager job openings in Monroe, NC as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 25% Part Time, 1% Temporary, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $75,396 per year, or $36.2 per hour.

Quality Control Analyst

Glenmark Pharmaceuticals

Monroe, NC • On-site

$22.25 - $30/hr

Full-time

Posted 28 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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