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Quality Assurance Associate I Jobs (NOW HIRING)

Strides Pharma Inc

QA Associate I

Chestnut Ridge, NY · On-site

$22 - $26/hr

POSITION SUMMARY The Quality Associate I, Operations is responsible for actively participating in ... Assurance experience preferred) Knowledge & Skills * Ability to communicate and work with teams

Karius

Quality Assurance Associate

Redwood City, CA · On-site

The Quality Assurance Associate must demonstrate a high level of individual responsibility and accountability and possess the ability to perform to the requirements listed below. The QA Associate ...

Karius

Quality Assurance Associate

Redwood City, CA · On-site

$41.47 - $62.21/hr

The Quality Assurance Associate must demonstrate a high level of individual responsibility and accountability and possess the ability to perform to the requirements listed below. The QA Associate ...

Karius

Quality Assurance Associate

Redwood City, CA

$41.47 - $62.21/hr

The Quality Assurance Associate must demonstrate a high level of individual responsibility and accountability and possess the ability to perform to the requirements listed below. The QA Associate ...

Avcend

Quality Assurance Associate

Reno, NV · On-site

$28.40/hr

Quality Assurance Associate Payrate: $28.85 / hr. on W2 Work Week   1 - Monday, 2 - Tuesday, 3 - Wednesday, 4 - Thursday, 5 - Friday Job Description/Comment: Responsible for all activities ...

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How much do quality assurance associate i jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for quality assurance associate i in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What is a quality assurance associate I?

A Quality Assurance Associate I is an entry-level professional responsible for assisting with the maintenance and enforcement of quality standards within an organization, typically in industries like pharmaceuticals, manufacturing, or food production. Their duties often include inspecting products or processes, documenting findings, supporting audits, and ensuring compliance with regulatory requirements. They work under the direction of more senior quality assurance staff to help identify and resolve quality issues, contributing to the overall reliability and safety of the company's products or services.

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

To thrive as a Quality Assurance Associate I, you need a solid understanding of quality control principles, attention to detail, and a bachelor's degree in a scientific or technical field. Familiarity with quality management systems (QMS), documentation software, and regulatory guidelines such as GMP or ISO standards is typically required. Strong analytical thinking, effective communication, and teamwork skills help you identify issues and collaborate with cross-functional teams. These abilities are crucial for maintaining product standards, ensuring compliance, and supporting continuous improvement within the organization.

What are some common challenges faced by a quality assurance associate I and how can they be managed effectively?

As a Quality Assurance Associate I, you may encounter challenges such as balancing multiple testing projects with tight deadlines, understanding evolving regulatory requirements, and ensuring effective communication with cross-functional teams. To manage these effectively, it's important to prioritize tasks, stay organized with detailed documentation, and proactively seek clarification when requirements are unclear. Building strong relationships with colleagues in production, research, and regulatory departments also helps ensure smooth workflow and quick resolution of issues.

What is the difference between Quality Assurance Associate I vs Quality Control Technician?

AspectQuality Assurance Associate IQuality Control Technician
CredentialsTypically requires a bachelor's degree in life sciences or related fieldOften requires a diploma or associate degree in a technical field
Work EnvironmentInvolves documentation, process audits, and compliance activities within labs or manufacturingFocuses on testing, sampling, and inspecting products or materials
Industry UsageCommonly used in pharmaceutical, biotech, and manufacturing industries

The main difference is that a Quality Assurance Associate I focuses on ensuring processes meet quality standards through documentation and audits, while a Quality Control Technician primarily tests and inspects products to identify defects. Both roles are essential in maintaining product quality but differ in their specific responsibilities and focus areas.

What cities are hiring for Quality Assurance Associate I jobs?

Cities with the most Quality Assurance Associate I job openings:

What states have the most Quality Assurance Associate I jobs?

States with the most job openings for Quality Assurance Associate I jobs include:

What are popular job titles related to Quality Assurance Associate I jobs?

For Quality Assurance Associate I jobs, the most frequently searched job titles are:

Quality Assurance Associate I jobs near you

QA Associate I

Chestnut Ridge, NY • On-site

Strides Pharma Inc
See more jobs at Strides Pharma Incexternal

$22 - $26/hr

Full-time

Re-posted 20 days ago

Key responsibilities

  • Perform physical inspection of in-process and finished product samples according to the production schedule.

  • Collect samples from manufacturing and packaging, label them appropriately, and submit to archive storage.

  • Respond to and escalate non-conforming events identified during production to Quality Management.

Job description

POSITION SUMMARY

The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging. Quality activities include product sampling and inspection, area clearance to confirm process readiness, non-conforming event support to resolve in-process issues. Communicates to multiple departments and supervision to provide timely process and issue updates. Identifies and escalates issues or problems to appropriate supervision. Participates as a team member on cross-functional teams. Participates in reviews and structured processes for continuous improvement. 

 

ESSENTIAL FUNCTIONS

Quality Operations 

  • Performs physical inspection of in-process and finished product samples as assigned and according to the production schedule. 
  • Collects samples from manufacturing and packaging according to the defined Batch Production Record and procedure requirements 
  • Becomes competent in processes: Weighing, Blending, Granulation, Compression, Coating, Encapsulation, Packaging. 
  • Follows internal processes related to controlled substances 
  • Performs GMP-related verifications such as line clearances, cleaning, room inspection, and materials. 
  • Collects and appropriately labels packaging retain samples, and submits to the archive storage. 
  • May execute computer data entries in CME, JDE, LIMS, and department databases 
  • Collects retain samples and performs sample evaluation for Annual Product Review 
  • May backup third party product review/release 
  • Perform sampling of Active Pharmaceutical Ingredients, excipients, and packaging components or release testing

 

Non-Conforming Events 

  • Responds to and escalates events identified during production to Quality Management 
  • Participates in investigations with the Rapid Response Team as needed 



Process Improvement 

  • Collaborates with Manufacturing and Quality partners to identify and implement improvements 


Compliance 

  • Conducts GMP walkthroughs of facilities 
  • Learns how to perform in-process audits to identify adherence to SOPs and BPR requirements 
  • Actively participates in training events, and maintains currency with assigned training requirements 

Safety 

  • Follows all procedures to ensure a safe and compliant work environment. 


QUALIFICATIONS

Education & Experience 

  • High school diploma or equivalent with 2-4 years’ relevant industry (Oral Solid Dose pharmaceutical manufacturing and Quality Assurance experience preferred)


Knowledge & Skills 

  • Ability to communicate and work with teams 
  • Attention to detail 
  • Strong documentation skills 
  • Ability to read and interpret SOPs and function within the scope of procedures 
  • Proficiency with basic math skills and basic experience with computers and software applications required 
  • Ability to learn new processes and procedures
  • Able to communicate effectively with other departments, management and operational personnel 
  • Customer/Stakeholder focused (understands impact of daily work to compliance and overall business) 
  • Proof-reading skills; ability to identify errors 
  • Ability to read and comprehend documentation and requirements set forth in Batch Production Records (BPRs)
  • Experience with Enterprise Resource Planning (ERP) system is a bonus
  • Ability to work overtime as needed, including occasional weekend shifts


Physical Requirements

  • Lift 15 lbs. 
  • Walk across plant/warehouse 
  • Wear appropriate gowning as required 
  • Ability to read for extended periods of time