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Quality Control In Jobs (NOW HIRING)

Martin Marietta

Quality Control Technician

Alden, IA

$19.25 - $24.50/hr

The QC Tech uses prescribed standards to determine gradational and/or physical characteristics for ... Work in and around aggregate processing plants to obtain material samples from conveyors ...

Skilled Up Solutions

Quality Control

Madison, IN

$25 - $27/hr

Quality Control Job DescriptionOverview Join our dynamic team in Madison, IN, where we prioritize excellence and innovation! As a Quality Control professional, you will play a vital role in ensuring ...

New

SU Solutions

Quality Control

Madison, IN · On-site

$25 - $27/hr

Quality Control Overview Join our dynamic team in Madison, IN, where we prioritize excellence and innovation! As a Quality Control professional, you will play a vital role in ensuring our products ...

New

HI-TECH ENGINEERING PARTNERS LLC

QC

West Lafayette, IN · On-site

$70K - $120K/yr

S. Semiconductor Factory Construction in West Lafayette IN Job Summary We are seeking an experienced CSA Quality Control Inspector to ensure the highest standards of quality in the construction of ...

Corbion

Manager, QA/QC

Blair, NE

As our next QA/QC Manager, you will be a member of the Blair management team, take part in the ... In addition, you will effectively manage the annual QA Department budget. Essential Job Functions:

corbion

Manager, QA/QC

Blair, NE

As our next QA/QC Manager, you will be a member of the Blair management team, take part in the ... In addition, you will effectively manage the annual QA Department budget. Essential Job Functions:

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Quality Control In information

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$30.5K

$81.3K

$129.5K

How much do quality control in jobs pay per year?

As of May 30, 2026, the average yearly pay for quality control in in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Quality Control Inspector, you need a solid understanding of quality assurance principles, attention to detail, and familiarity with industry standards, often supported by a high school diploma or technical certification. Experience with measurement tools (such as calipers and micrometers), inspection software, and knowledge of ISO standards are typically required. Strong analytical thinking, effective communication, and problem-solving skills set top performers apart in this role. These abilities are crucial for ensuring product consistency, meeting regulatory requirements, and maintaining customer satisfaction.

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

Quality Control Inspectors often encounter challenges such as identifying subtle defects, maintaining consistency across large batches, and managing tight deadlines. Effective communication with production teams and a thorough understanding of product specifications are crucial for addressing these challenges. Leveraging checklists, standardized procedures, and ongoing training can help inspectors stay accurate and efficient. Additionally, embracing new quality management technologies can improve inspection processes and facilitate collaboration with other departments.

What are Quality Control Inspectors?

Quality Control Inspectors are professionals responsible for examining and testing products or materials to ensure they meet established quality standards and specifications. They work in various industries, including manufacturing, food production, and pharmaceuticals, using specialized tools and techniques to detect defects or deviations. Their role is vital in maintaining product safety, compliance, and customer satisfaction by identifying issues early in the production process. Inspectors document their findings, recommend improvements, and sometimes help implement corrective actions. Their work helps organizations maintain high-quality standards and avoid costly recalls or customer complaints.

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

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

More about Quality Control In jobs
What cities are hiring for Quality Control In jobs? Cities with the most Quality Control In job openings:
What states have the most Quality Control In jobs? States with the most job openings for Quality Control In jobs include:
What job categories do people searching Quality Control In jobs look for? The top searched job categories for Quality Control In jobs are:
Quality Control In jobs near you
Infographic showing various Quality Control In job openings in the United States as of May 2026, with employment types broken down into 86% Full Time, 8% Part Time, 3% Temporary, and 3% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Quality Control Manager

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Posted 10 days ago

Job description

Quality Control Manager The Quality Control (QC) Manager plays a pivotal role in ensuring that QC is effectively serving in its support role to clinical and commercial production. The QC Manager will ensure that analytical testing for process check points, stability, and release assays are being carried out to certify that quality standards are upheld for all products produced at the facility. The goal is to ensure that the Quality Control group and company is constantly moving towards fulfilling its short-term and long-term objectives and does not diverge from its strategic guidelines. Under the direction of the VP, Global Quality Head, responsibilities of the QC Manager will include but are not limited to:
  • Leading, hiring, developing, training, and evaluating QC personnel
  • Devising sound hiring strategies based on business needs
  • Supervising and overseeing QC personnel in their roles for safe and efficient verification, approval, release/disposition of HCATS and/or client products/materials
  • Delegating responsibilities and supervising the work of laboratory personnel, while providing guidance and motivation to drive maximum performance
  • Ensuring and promoting compliance with applicable cGMP and GTP regulations, while ensuring compliance with company and client methodologies
  • Assuring alignment and efficient continuity in laboratory practices between sites
  • Serving as approver in investigations while overseeing timely closure of deviation reports, change controls, CAPAs, and applicable batch records
  • Ensuring completion of all client QC requirements related to GMP cellular products and/or materials
  • Overseeing QC role in material dispositions via deviation reporting system, CoAs, and/or client-based systems, if applicable
  • Prioritizing, scheduling, and managing multiple projects and resources simultaneously
  • Monitoring effectiveness of quality systems, change control activities and their completion, for both, internal and client audit findings
  • Evaluating and investigating customer complaints and deviations; coordinating corrective and preventive actions as they relate to the Quality Control function
  • Delegating maintenance, tracking, and trending aspects of the deviation reporting system
  • Developing and maintaining Key Performance Indicators (KPIs) for laboratory testing
  • Interfacing with vendors, suppliers, and in-house production personnel to ensure effective corrective and preventive actions are implemented for recurring product/process discrepancies, when applicable
  • Interfacing with management at all levels for alignment on significant deviation resolution and corrective action implementation
  • Delegating development, revisions, and implementation of Standard Operating Procedures as related to Quality Control activities
  • Participating in and tracking group budget setting and cost containment drives
  • Communicating and maintaining trust relationships with senior management, business partners, and clients
  • Ensuring company policies and legal guidelines are communicated top-down in the company and that they are followed at all times
  • Completing projects and special tasks as assigned by the Global Quality Head
  • Off-schedule shifts during weekends and holidays based on business requirements a possibility
  • On-call presence preferred while physical personal presence is not possible
  • Candidate will oversee QC Scientist and QC Associate I, II, and III roles. The QC Manager will delegate responsibilities to direct reports to achieve the requisite business needs, while providing ongoing support to Manufacturing processes.
REQUIREMENTS
  • BA/BS/MS in a science or relevant field required
  • Master’s in Business Administration or relevant field will be preferred
  • 7 – 10 years’ experience in the pharmaceutical, biologics or related industry
  • Prior cGMP experience required
  • Prior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a CGMP/GTP environment a must
  • Experience in Flow Cytometry is a must
  • 5 + Years experience leading a team is a must. Proven ability to lead, coach, and motivate employees, clearly communicate job requirements and effectively manage performance of assigned staff
  • Sound understanding of current Good Manufacturing Practices (cGMPs)
  • Working knowledge of routine QC laboratory procedures such as flow cytometry and CBC analysis, endotoxin testing, equipment and systems, and understanding of production processes and validation
  • Prior experience with reviewing Standard Operating Procedures, work instructions, protocols, methods, method validations preferred
  • Proven experience in a supervisory or managerial position
  • Demonstrable experience in developing strategic plans based on business needs
  • Strong understanding of Quality Control in pharmaceutical/biotechnology/biologics industries
  • Thorough knowledge of market changes and forces that influence the company
  • Proficient with computer software: Microsoft Office, Visio
  • Strong written, oral, and presentational skills
  • Strong knowledge of QC Analytical testing methodologies, philosophies, method validation and method transfers
  • Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review
  • Excellent organizational and leadership skills
  • Excellent communication, interpersonal, and presentation skills
  • Outstanding analytical and problem-solving abilities
  • Strong business acumen
  • Ability to think strategically, tactically (detail-oriented), and advise personnel in an effective manner
  • Candidate must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities
While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noisy. Must have the ability to work in a team-oriented environment and with clientsMust be able to handle the standard/moderate noise of the manufacturing facility Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.