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Quality Control Control Jobs in Clifton, NJ (NOW HIRING)

Actalent

QC Investigator

Orangeburg, NY

$45 - $50/hr

QC Investigator Book here for more info! The QC Investigator is responsible for the oversight and execution of complex and critical Phase I and Phase II investigations related to quality control (QC) ...

CookUnity

Quality Control Supervisor

New York, NY · On-site

The Role The Quality Control Supervisor is responsible for overseeing the performance of the QC area, ensuring compliance with operational procedures, and driving continuous improvement across all ...

OnScent

Quality Control Technician

Norwood, NJ

$60K - $68K/yr

The Quality Control Technician is responsible for inspecting, evaluating, and analyzing/testing the raw materials and finished products by performing basic sensory and/or analytical tests to ensure ...

PDI (NY)

QC Investigator

Orangeburg, NY · On-site

$24.25 - $32.75/hr

POSITION PURPOSE The QC Investigator provides the leadership and technical expertise necessary to establish robust investigations during laboratory events, out of specification, and out of trend ...

OnScent

Quality Control Technician

Norwood, NJ

$60K - $68K/yr

The Quality Control Technician is responsible for inspecting, evaluating, and analyzing/testing the raw materials and finished products by performing basic sensory and/or analytical tests to ensure ...

ExtensisHR

Quality Control Technician

Norwood, NJ

$60K - $68K/yr

The Quality Control Technician is responsible for inspecting, evaluating, and analyzing/testing the raw materials and finished products by performing basic sensory and/or analytical tests to ensure ...

PDI

QC Investigator

Orangeburg, NY · On-site

$24.25 - $32.75/hr

POSITION PURPOSE The QC Investigator provides the leadership and technical expertise necessary to establish robust investigations during laboratory events, out of specification, and out of trend ...

CookUnity

Quality Control Associate

New York, NY

The Role As a Quality Control (QC) Associate at CookUnity, you play a key role in ensuring the quality, accuracy, and presentation of meals throughout the production process. You'll support the QC ...

TekSky

Quality Control Inspector

Caldwell, NJ · On-site

Quality Control Inspector West Caldwell, NJ Selco Manufacturing Corp. provides structural and miscellaneous steel fabrication. As an AISC-certified company for Bridge Structures, Selco is recognized ...

OnScent

Quality Control Technician

Norwood, NJ · On-site

$60K - $68K/yr

The Quality Control Technician is responsible for inspecting, evaluating, and analyzing/testing the raw materials and finished products by performing basic sensory and/or analytical tests to ensure ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

BERJE INCORPORATED

QC Analyst

Carteret, NJ

$26 - $31/hr

Reporting to the Quality Control leadership team, the Quality Control Analyst is responsible for performing analytical testing of raw materials, intermediates, and finished products to ensure ...

System One

QC Analyst

Orangeburg, NY · On-site

$22 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $22.00 to $23.00 Work Model: Onsite - onsite Hours: 6:00am to 2:30pm Responsibilities * Perform analyses of Clinical ...

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Quality Control Control information

See Clifton, NJ salary details

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How much do quality control control jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for quality control control in Clifton, NJ is $22.09, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $24.71 per hour, depending on experience, location, and employer.

Is quality control a good career choice?

Quality control is a viable career option that involves inspecting products or services to ensure they meet standards, often requiring attention to detail and knowledge of industry regulations. It can lead to roles in manufacturing, healthcare, or software, with opportunities for advancement and certification such as Six Sigma or ISO auditor training.

What does a quality control job do?

A quality control job involves inspecting products or services to ensure they meet specified standards and quality requirements. It often includes testing, measuring, and documenting findings, and may require knowledge of quality management systems and tools like checklists or testing equipment.

What cities near Clifton, NJ are hiring for Quality Control Control jobs?

Cities near Clifton, NJ with the most Quality Control Control job openings:

Quality Control Control jobs near you

Quality Control Manager

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Re-posted 7 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.