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Change Control Manager Jobs in Ruby, SC (NOW HIRING)

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

... 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 ...

QA/QC Lead - Solar Role Type: Full-Time Reporting To: QA/QC Manager / Project Manager Project Sites ... Plans are realistic, promises are kept, and issues are surfaced early when conditions change.

Salary: QA/QC Lead Solar Role Type: Full-Time Reporting To: QA/QC Manager / Project Manager Project ... Plans are realistic, promises are kept, and issues are surfaced early when conditions change.

QA/QC Lead - Solar Role Type: Full-Time Reporting To: QA/QC Manager / Project Manager Project Sites ... Plans are realistic, promises are kept, and issues are surfaced early when conditions change.

Manufacturing Engineer I

Monroe, NC · On-site

$67K - $87K/yr

... control activities for Change Control in the department. • Resolves issues and delays in ... Management. • Proven ability to analyze and troubleshoot production processes. • Project ...

Mid-Senior Mechanical Engineers

Hartsville, SC · Remote

$107K - $141K/yr

... engineering change control processes in nuclear environments * Excellent problem-solving, analytical, and technical skills * Strong written and verbal communication skills * Ability to manage ...

Mid-Senior Mechanical Engineers

Hartsville, SC · Remote

$107K - $141K/yr

... engineering change control processes in nuclear environments * Excellent problem-solving, analytical, and technical skills * Strong written and verbal communication skills * Ability to manage ...

Mid-Senior Mechanical Engineers

Hartsville, SC · Remote

$107K - $141K/yr

... engineering change control processes in nuclear environments * Excellent problem-solving, analytical, and technical skills * Strong written and verbal communication skills * Ability to manage ...

Senior Manufacturing Engineer

Monroe, NC · On-site

$84K - $115K/yr

Lead and manage the Manufacturing Engineering team of 4, including: * 1 Level I Engineer * 1 Level ... Initiate and follow up on Change Control processes for department operations * Coordinate and ...

Continuous Improvement Manager

Monroe, NC · On-site

$87K - $117K/yr

Lead data-driven analysis using statistical tools (e.g., Pareto, regression, control charts, and ... Change Leadership: Effective in driving adoption and managing organizational change * Risk ...

Continuous Improvement Manager

Monroe, NC

$87K - $117K/yr

Lead data-driven analysis using statistical tools (e.g., Pareto, regression, control charts, and ... Change Leadership: Effective in driving adoption and managing organizational change * Risk ...

Continuous Improvement Manager

Monroe, NC · On-site

$87K - $117K/yr

Lead data-driven analysis using statistical tools (e.g., Pareto, regression, control charts, and ... Change Leadership: Effective in driving adoption and managing organizational change * Risk ...

This includes all cost controls, inventory control, cash control and customer relations. You must ... Must be able to make correct monetary change. * Verbal, writing, and telephone skills to take and ...

This includes all cost controls, inventory control, cash control and customer relations. You must ... Must be able to make correct monetary change. * Verbal, writing, and telephone skills to take and ...

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Showing results 1-20

Change Control Manager information

See Ruby, SC salary details

$35.2K

$74.1K

$112.3K

How much do change control manager jobs pay per year?

As of Jul 6, 2026, the average yearly pay for change control manager in Ruby, SC is $74,096.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,900.00 and $109,200.00 per year, depending on experience, location, and employer.

What are the typical challenges faced by a Change Control Manager when coordinating cross-functional teams during change implementation?

A Change Control Manager often encounters challenges such as aligning diverse team priorities, ensuring clear communication, and managing resistance to change across departments. Coordinating cross-functional teams requires balancing the needs and schedules of stakeholders in IT, quality assurance, operations, and regulatory affairs. Successfully navigating these challenges involves setting transparent processes, hosting regular update meetings, and fostering a culture of collaboration to ensure changes are implemented smoothly and in compliance with relevant standards.

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

To thrive as a Change Control Manager, you need expertise in project management, process improvement, and risk assessment, often supported by a relevant degree and certifications such as PMP or ITIL. Familiarity with change management software, documentation systems, and compliance tools is typically required. Strong communication, analytical thinking, and stakeholder management skills help drive successful change initiatives and mitigate resistance. These skills and qualities are crucial to ensure that organizational changes are implemented efficiently, with minimal disruption and maximum compliance.

What is the difference between Change Control Manager vs Quality Assurance Specialist?

AspectChange Control ManagerQuality Assurance Specialist
CertificationsISO 9001, PMP, or equivalentISO 9001, Six Sigma, or equivalent
Work EnvironmentRegulated industries like manufacturing, pharma, biotechManufacturing, software, healthcare sectors
Primary FocusManaging change processes, documentation, approvalsEnsuring product quality, testing, compliance

The Change Control Manager and Quality Assurance Specialist roles often overlap in regulated industries, but their focus differs. The Change Control Manager primarily oversees change processes and documentation, ensuring compliance with procedures. The Quality Assurance Specialist concentrates on maintaining product quality through testing and compliance checks. Both roles require similar certifications and work environments, but their core responsibilities distinguish them within the industry.

What are Change Control Managers?

Change Control Managers are professionals responsible for overseeing and managing the process of controlling changes to projects, systems, or processes within an organization. Their main role is to ensure that all proposed changes are properly evaluated, documented, and implemented in a controlled manner to minimize risks or disruptions. They work closely with project teams, stakeholders, and quality assurance to ensure compliance with regulatory requirements and organizational standards. This role is especially vital in industries like IT, pharmaceuticals, and manufacturing, where changes can significantly impact operations or product quality.
What job categories do people searching Change Control Manager jobs in Ruby, SC look for? The top searched job categories for Change Control Manager jobs in Ruby, SC are:
What cities near Ruby, SC are hiring for Change Control Manager jobs? Cities near Ruby, SC with the most Change Control Manager job openings:
Infographic showing various Change Control Manager job openings in Ruby, SC as of June 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $74,096 per year, or $35.6 per hour.

Quality Control Analyst

Glenmark Pharmaceuticals

Monroe, NC • On-site

$22.25 - $30/hr

Full-time

Posted 7 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.