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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 ...

Goodwill Industries of Greater New York and Northern New Jersey

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E-Commerce Quality Control Associate

South Hackensack, NJ · On-site

$17 - $20/hr

Position Overview The Authentication Associate plays a critical role in ensuring the integrity of ... Stay informed on emerging counterfeit trends and evolving replica quality across categories E ...

Goodwill Industries of Greater New York and Northern New Jersey

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E-Commerce Quality Control Associate

South Hackensack, NJ · On-site

$17 - $20/hr

Position Overview The Authentication Associate plays a critical role in ensuring the integrity of ... Stay informed on emerging counterfeit trends and evolving replica quality across categories E ...

Express Employment Professionals

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Quality Assurance & Supply Chain Associate

Franklin Lakes, NJ · On-site

$65K - $75K/yr

Quality Assurance & Supply Chain Associate Location: Franklin Lakes, NJ Schedule: Monday-Friday, 8:00 AM - 5:00 PM Salary: $65,000 - $75,000 per year About the Role We are seeking a detail-oriented ...

The Chefs' Warehouse

Produce Quality Control

Bronx, NY

$23/hr

... associates, best-in-breed technology, rapid service, and support levels that solidify our long ... The Produce QC team member will assist in maintaining the highest quality produce, consistent with ...

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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Quality Associate information

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$11

$27

$51

How much do quality associate jobs pay per hour?

As of Jun 15, 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.

Is QA a difficult job?

Quality Associate roles can be challenging as they require attention to detail, understanding of quality standards, and often involve repetitive tasks and strict compliance requirements. Success in the role depends on strong analytical skills, knowledge of testing procedures, and sometimes certifications like Six Sigma or ISO standards.

Is QC a high paying job?

Quality Associate positions typically offer average salaries that are competitive within manufacturing and production industries, but they are generally not considered high-paying roles. Salary levels depend on factors such as experience, location, and industry, with some roles offering opportunities for advancement and certification that can increase earning potential.

What are Quality Associates?

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 jobs pay 10,000 a month without a degree?

A Quality Associate typically earns less than $10,000 a month, but high-paying roles in sales, real estate, or skilled trades can reach or exceed that level without a degree. These jobs often require experience, certifications, or specialized skills and may involve variable income or commission-based pay structures.

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 is the job of a quality associate?

A quality associate is responsible for inspecting products, monitoring manufacturing processes, and ensuring compliance with quality standards. They often use testing tools and follow procedures to identify defects and improve product quality. Strong attention to detail and knowledge of quality management systems are essential for this role.

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

Quality Assurance Associate III

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Posted 10 days ago

Job description

Quality Assurance Associate IIIAllendale, 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 Assurance Associate III is responsible for performing Quality Assurance activities within minimal supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, issuance, review and approval of batch records, SOPs, Qualification and Validation Reports; review of QC data; perform material releases and final product releases; review of Deviations as well as assists Quality management with department needs. He/she exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. This role manages internal and external audits which may include interaction with Health Authorities and clients
  • Interfaces directly with client and cross functional teams
  • Provides resolutions pertaining to quality for project related issues
  • Independently prioritize, schedule, and manage multiple projects and resources (team)
  • Ensures the safe release of cellular products in accordance with company and/or client procedures and requirements.
  • Ensure and promote compliance with applicable CGMP and GTP regulations and company and client SOPs
  • Able to provide input based on knowledge and experience on quality systems and procedures and CGMP/GTP issues.
  • Author and review relevant SOPs, validation and other documents.
  • Responsible for the timely issuance, review and approval of QC certificates, closure of Batch Records, and deviation reports.
  • Responsible for the completion of all client requirements related to cellular product and/or material releases.
  • Master Batch Record Control, distribution and label verification
  • Perform line clearance activities as required.
  • Assignment and maintenance of product Lot numbers as applicable.
  • Perform internal documentation audits as assigned.
  • Materials management nonconformance disposition and release activity as applicable.
  • Responsible for accurate deviation reporting as applicable and tracking/trending follow up actions to closures
  • Evaluate and investigate deviation reports and initiate and coordinate corrective and preventive actions.
  • Track and trend relevant quality metrics including environmental monitoring data.
  • Provide Quality Assurance related support to various departments.
  • Interface with suppliers and in-house production personnel to ensure effective corrective and preventive actions are implemented for recurring product/process discrepancies.
  • Electronic Document Control activities as assigned.
  • Provide training to personnel as assigned by supervisor.
  • Travel may be required.
REQUIREMENTS
  • BS in biological sciences or other relevant field of study
  • 5 years + experience in QA in a life sciences company company with a strong focus in the manufacturing and/or testing of biologics.
  • Working knowledge and technical understanding of aseptic manufacture of biologics
  • Understanding of quality system applications
  • Experience in both clinical and commercial manufacturing is preferred.
  • Experience in authoring, reviewing, and /or approving cGMP/cGTP related documents (validation/qualification reports, SOPS. Etc.
  • Experience in organizing teams for effective and timely completion of projects.
  • Understanding of quality system applications, including the use of electronic applications for training, deviations, CAPA management, etc.
  • Experience participating in or hosting health authority inspections and/or client audits.
  • Computer skills (Microsoft Office, Outlook)
  • Detail-oriented and organized
  • Analytical and problem-solving skills
  • Good written and oral communication skills
  • Ability to multi-task and be adaptable
  • Flexible and able to adapt to company growth and evolving responsibilities
  • Ability to work independently and with a team
  • Strong Project Management and organization skills
  • 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
May be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, etc. 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.