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Quality Associate Jobs in Spring Valley, NY (NOW HIRING)

Strides Pharma Inc

QA Associate (QMS)

Spring Valley, NY · On-site

$58K - $65K/yr

Position Summary The QA Associate supports the site's Quality Management System by managing product complaints, adverse events, and investigation activities. This role contributes to deviation and ...

Brilliant Earth

Quality Control Associate (Repairs)

Secaucus, NJ · On-site

$24/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Associate (Repairs) - Secaucus, NJ Our Operations team is dedicated to delivering excellence from the time a customer places an order to the moment a customer opens their package. The ...

Englewood Lab

Quality - Regulatory Affairs Associate

Totowa, NJ · On-site

$58K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality / Regulatory Reports To: Manager of Regulatory Affairs Position Summary The Regulatory Affairs Associate will assist the Manager of Regulatory Affairs with inspections and audits, ensuring ...

Sharp Electronics

Associate QA Analyst/Developer

Montvale, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Overview The Associate QA Analyst/Developer is responsible for MICAS and Synappx Manage support functions, including but not limited to creating SQL reports, testing systems, and the latest updates.

Sharp Electronics

Associate QA Analyst/Developer

Montvale, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Overview The Associate QA Analyst/Developer is responsible for MICAS and Synappx Manage support functions, including but not limited to creating SQL reports, testing systems, and the latest updates.

LHH US

Quality Engineer

Northvale, NJ

$50 - $65/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Engineer Location: Northvale, NJ (On-Site) Pay Rate: $50.00 - $65.00 per hour Employment ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

New

LHH US

Quality Engineer

Northvale, NJ

$50 - $65/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Engineer Location: Northvale, NJ (On-Site) Pay Rate: $50.00 - $65.00 per hour Employment ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

New

LHH US

Quality Inspector

Northvale, NJ

$25 - $29/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal ...

New

LHH US

Quality Inspector

Northvale, NJ · On-site

$25 - $29/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal ...

New

Nivoda

Logistics and QC Associate

New York, NY

$50K - $60K/yr

Salary $50,000 - $60,000 We are looking to hire an experienced Logistics and QC Associate for our New York office. You will be responsible for managing all incoming and outgoing shipments to and from ...

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Showing results 21-40

All JobsQuality Associate JobsQuality Associate Jobs in Spring Valley, NY

Quality Associate information

See Spring Valley, NY salary details

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How much do quality associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality associate in Spring Valley, NY is $27.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.92 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

What are the key skills and qualifications needed to thrive as a quality associate, and why are they important?

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Spring Valley, NY?

The most popular types of Quality jobs in Spring Valley, NY are:

What job categories do people searching Quality Associate jobs in Spring Valley, NY look for?

The top searched job categories for Quality Associate jobs in Spring Valley, NY are:

What cities near Spring Valley, NY are hiring for Quality Associate jobs?

Cities near Spring Valley, NY with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Spring Valley, NY as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $56,765 per year, or $27.3 per hour.

Quality Control Analytical Associate II

Lynkx Staffing LLC

Saddle Brook, NJ • On-site

Full-time

Re-posted 10 days ago

Job description

Quality Control Analytical Associate IIAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device, IT & Human Resources disciplines in New Jersey. The Quality Control Analytical Associate II serves as a support role to clinical and commercial production. The QC Analytical Associate II will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. Under the direction of the Manager, QC Analytical Associate II, responsibilities include:
  • Performs the accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or efficacy of different cell populations
  • Performs maintenance, monitoring, and troubleshooting of pertinent equipment
  • Performs and assists in the training of other Quality Control technicians
  • Maintains training records and coordinates records retention with Document Control and Training groups
  • Tests, documents, and reports results for products or materials following company and/or client procedures following CGMP and/or GTP guidelines
  • Performs state proficiency testing and/or client proficiency testing under direct supervision as applicable
  • Participates in managing QC materials and supplies
  • Performs and assists in equipment and method qualification/validation activities as needed
  • Performs reagent and media preparation
  • Provides input based on level of knowledge and experience with troubleshooting malfunctioning equipment
  • Investigates out-of-specification, out-of-trend, aberrant, and/or non-conforming test results
  • Initiates, investigates, and prepares deviation reports with input from assigned supervisor
  • Brainstorms and implements corrective and preventive actions, as and when applicable
  • Documents training and execution of shipping test samples to contract laboratories for testing
  • Completes all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
  • Communicates effectively with other co-workers, departments, management and clients
  • Eventually serves as a lead and/or co-lead for client projects
  • Additional tasks as assigned
REQUIREMENTS
  • BA/BS in a science or relevant field required
  • Prior cGMP experience required
  • Prior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a CGMP/GTP environment preferred
  • Prior industrial experience in cell count methodologies preferred
  • Prior academic and/or industrial cell therapeutic experience preferred
  • Minimum 2-5 years of experience in Quality Control laboratory setting or within the biopharmaceutical industry
  • Proficient with computer software such as: Microsoft Office, Visio
  • Strong written and oral communication skills
  • Strong presentational skills preferred
  • 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.
Other Information
  • 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 clients
  • Must be able to work during the weekend, holidays, and as required by the company
  • Must be able to handle the standard/moderate noise of the manufacturing facility
  • The QC Analytical Associate II must be able to work in a laboratory environment for an extended period.
  • Must be physically capable to stand; walk; sit; bend; stretch; use hands to finger, handle or feel; reach with hands and arms; and talk or hear
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. QC Analytical Associate I is available as well.