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Lab Quality Control Jobs in New Jersey (NOW HIRING)

Quality Control Technologist III

Warren, NJ · On-site

$19.50 - $25/hr

They schedule all testing activities in the lab and report status in daily update meetings. The ... Guides QC technicians training activities and ensures that the appropriate training records are ...

QUALITY CONTROL TECHNICIAN

Linden, NJ · On-site

$19.25 - $24.75/hr

Quality Control Related Responsibilities * Implement various analytical tests on incoming samples ... Maintain cleanliness of the lab according to Good Laboratory Practices. * Order supplies and ...

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

Job Title - Scientist I, QC Work Location - Cranbury, NJ Job Summary: We are seeking a self ... Conduct assays and lab procedures according to and in compliance with cGMP guidelines and internal ...

As our Quality Control Technician you will assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining ...

As our Quality Control Technician you will assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining ...

As our Quality Control Technician you will assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining ...

Support daily lab operation activities, including but not limited to lab equipment cleaning, lab ... years of industry quality control experience. * Or Master's degree in Analytical Chemistry ...

Quality Control Technologist III

Warren, NJ · On-site

$19.50 - $24.75/hr

They schedule all testing activities in the lab and report status in daily update meetings. The ... Guides QC technicians training activities and ensures that the appropriate training records are ...

Perform equipment checks and safety monitoring * Assist in maintaining the lab's quality control system * Sterilize microbiological waste and biohazards * Adhere to GMP and safety standards; report ...

Perform equipment checks and safety monitoring * Assist in maintaining the lab's quality control system * Sterilize microbiological waste and biohazards * Adhere to GMP and safety standards; report ...

Perform equipment checks and safety monitoring * Assist in maintaining the lab's quality control system * Sterilize microbiological waste and biohazards * Adhere to GMP and safety standards; report ...

Perform equipment checks and safety monitoring * Assist in maintaining the lab's quality control system * Sterilize microbiological waste and biohazards * Adhere to GMP and safety standards; report ...

Perform equipment checks and safety monitoring * Assist in maintaining the lab's quality control system * Sterilize microbiological waste and biohazards * Adhere to GMP and safety standards; report ...

Perform equipment checks and safety monitoring * Assist in maintaining the lab's quality control system * Sterilize microbiological waste and biohazards * Adhere to GMP and safety standards; report ...

Showing results 41-60

Lab Quality Control information

See New Jersey salary details

$14

$22

$31

How much do lab quality control jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for lab quality control in New Jersey is $22.96, according to ZipRecruiter salary data. Most workers in this role earn between $19.28 and $24.42 per hour, depending on experience, location, and employer.

What is lab quality control?

Lab Quality Control refers to the processes and procedures used in laboratories to ensure the accuracy, reliability, and consistency of test results. Professionals in this field monitor equipment, follow standardized protocols, and analyze samples to detect errors or inconsistencies. They play a crucial role in maintaining compliance with regulatory standards and ensuring that laboratory outcomes are trustworthy. Effective quality control helps prevent inaccurate results, which can impact scientific research, medical diagnoses, and industrial processes.

What are the key skills and qualifications needed to thrive as a lab quality control professional?

To thrive in Lab Quality Control, you need a solid background in laboratory science, attention to detail, and familiarity with quality assurance protocols, often supported by a degree in chemistry, biology, or a related field. Proficiency with laboratory information management systems (LIMS), analytical instruments, and understanding of relevant regulatory standards (such as ISO 17025 or GMP) is typically required. Strong problem-solving, organizational, and communication skills help professionals effectively manage testing processes and collaborate with team members. These skills ensure accurate results, regulatory compliance, and the reliability of laboratory operations.

What are some common challenges faced in a lab quality control role and how can they be managed?

Lab Quality Control professionals often encounter challenges such as maintaining consistent adherence to strict protocols, managing tight deadlines for sample testing, and troubleshooting unexpected equipment or process issues. Working in this role requires strong attention to detail and effective communication with both lab technicians and management to ensure results are accurate and compliant with regulatory standards. To manage these challenges, it's important to stay organized, keep up with ongoing training, and foster collaborative relationships with colleagues from other departments like production and R&D.

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

AspectLab Quality ControlLab Technician
Primary RoleEnsures lab processes and products meet quality standardsPerforms tests and procedures in the lab
CertificationsOften requires quality assurance or related certificationsTypically requires a technical diploma or associate degree
Work EnvironmentQuality assurance labs, manufacturing, or clinical settingsResearch labs, clinical labs, or industrial labs
ResponsibilitiesDeveloping, implementing, and monitoring quality protocolsConducting tests, recording data, maintaining equipment

Lab Quality Control specialists focus on maintaining and improving lab quality standards, while Lab Technicians perform the hands-on testing and data collection. Both roles are essential in lab operations but differ in scope and responsibilities.

How to become a lab quality control technician?

To become a lab quality control technician, typically a high school diploma or equivalent is required, with many employers preferring an associate's degree or higher in fields like biology, chemistry, or related sciences. Relevant skills include attention to detail, knowledge of laboratory procedures, and familiarity with quality standards and testing equipment; certifications such as ASQ Quality Technician can enhance job prospects. On-the-job training is common, and the role often involves working in a laboratory environment with adherence to safety protocols.

Is lab quality control a good career?

Lab quality control is a vital role in ensuring the safety and efficacy of products in industries like pharmaceuticals, food, and manufacturing. It involves analyzing samples, maintaining compliance with regulations, and often requires certifications such as ISO or GMP. The field offers stable employment with opportunities for advancement and specialization.

What are popular job titles related to Lab Quality Control jobs in New Jersey?

For Lab Quality Control jobs in New Jersey, the most frequently searched job titles are:

Infographic showing various Lab Quality Control job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $47,756 per year, or $23 per hour.

Quality Control Technologist III

Werfen

Warren, NJ • On-site

$19.50 - $25/hr

Full-time

Re-posted 21 days ago


Werfen rating

8.7

Company rating: 8.7 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Introduction
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and bio-materials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.
Overview
Job Summary
This job is a lead role in the quality control laboratory, performing routine activities and assisting the manager in daily operations. This person knows how to execute all test methods performed in the lab. They schedule all testing activities in the lab and report status in daily update meetings. The train new employees, perform OOS and root cause investigations, perform data/record review, lead projects, and updates WIN/SOPs.
Responsibilities
Key Accountabilities
  • Provides direction and guidance to Quality Control staff in the performance of daily tasks. Creates daily and weekly scheduling of all QC related activities
  • Performs and schedules testing for incoming raw material, in-process, final release and inspection of BioArray products according to approved Standard Operating Procedures (SOP's) and other applicable documents within defined timeframes. Performs and schedules stability, method validations, equipment validations, threshold analysis process and other special testing.
  • Act as OJT trainer to train new employees and current employees on new test methods. Guides QC technicians training activities and ensures that the appropriate training records are completed as per the role functions
  • Reports and escalates out-of-specification results and deviations to the department supervisor/manager. Assists and leads the investigations, root cause analyses, and reports for out-of-specification results and deviations.
  • Writes/Revises SOPs, WI, QC Specification/testing documents. Maintains accurate, legible, and complete records according to Current Good Manufacturing Procedures (cGMP's).
  • Performs all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. Blood borne pathogens and chemical hazards).
  • Maintains work area, equipment, department, and all storage areas in a clean, neat, and orderly manner. Performs, schedules and delegates equipment calibration and manintenance.
  • Performs data review of QC test data. Works with quality assurance (QA) to ensure batch records are approved in a timely manner.
  • Stay up-to-date on medical device regualtions. Participate in internal and external audits.
  • Performs other duties and responsibilities as assigned

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Networking/Key relationships
This role will ineract with the following areas within the company (at a minimum):
  • Quality Assurance and Quality Control
  • Operations
  • Regulatory Affairs
  • Technical Support and R&D

This role may ineract with the following external partners:
  • External auditors
  • Regulatory agencies

Qualifications
Minimum Knowledge & Experience required for the position:
  • Bachelor's degree in biology or chemistry or related field. Five (5) or more years experience in a medical device or pharmaceutical GMP quality control laboratory. Experience working under 21 CFR Part 210/211 and/or 820 regulations required. Knowledge of ISO 13485 desired.
  • Two (2) or more years of experience performing out of specification (OOS) and/or root cause investigations (RCI) required. Experience with test method validation, performing data trending, and writing/revising SOP/WIN preferred.
  • Experience performing OOS Phase I investigations, in alignment with FDA guidelines, required.
  • Experience training QC technicians desired.
  • Experience performing PCR (Polymerase chain reaction) desired.
  • Experience in internal/external audits is a plus.

Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.
Skills & Capabilities:
  • Ability to accurately pipette solutions from 0.01 ul up to 10 ml.
  • Critical thinking and problem solving abilities
  • Ability to learn and work with software programs (off-the shelf and company designed)
  • Ability to work in a GMP lab environment, including donning the appropriate PPE (personnel protective equipment)
  • Overtime work may be required (occaissionally)
  • Ability to lead others to complete tasks and projects

Travel requirements:
No travel is required for this position.
Closing
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.
www.werfen.com

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About Werfen

Sourced by ZipRecruiter

Industry

Health care and social assistance

Company size

1,001 - 5,000 Employees

Headquarters location

L'Hospitalet de Llobregat, Barcelona, ES