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Quality Associate Ii Jobs (NOW HIRING)

Biocytogen

Quality Associate

Waltham, MA · On-site

We are seeking a detail-oriented and motivated Quality Associate to join our team. In this role ... Experience: 0-2 years of experience in a laboratory, quality, or clinical setting (Industry ...

Quest Global

Quality Associate

East Hartford, CT · On-site

$23 - $27/hr

Quality Associate Who We Are: Quest Global delivers world-class end-to-end engineering solutions by ... Bring: * 2-4 years of direct experience performing Quality, Manufacturing, or Supply Chain ...

Quest Global

Quality Associate

East Hartford, CT

$23 - $27/hr

Quality Associate Who We Are: Quest Global delivers world-class end-to-end engineering solutions by ... Bring: * 2-4 years of direct experience performing Quality, Manufacturing, or Supply Chain ...

Quest Global

Quality Associate

East Hartford, CT

$23 - $27/hr

Quality Associate Who We Are: Quest Global delivers world-class end-to-end engineering solutions by ... Bring: * 2-4 years of direct experience performing Quality, Manufacturing, or Supply Chain ...

Quest Global

Quality Associate

East Hartford, CT · On-site

$23 - $27/hr

Quality Associate Who We Are: Quest Global delivers world-class end-to-end engineering solutions by ... Bring: * 2-4 years of direct experience performing Quality, Manufacturing, or Supply Chain ...

Avient Corporation

Quality Associate

Avon Lake, OH · On-site

$19/hr

As a Quality Associate with Avient, you are responsible for testing product batches and will make ... Two weeks of vacation pro-rated based on start date, in addition to sick time, paid holidays ...

Avient

Quality Associate

Avon Lake, OH · On-site

As a Quality Associate with Avient, you are responsible for testing product batches and will make ... Two weeks of vacation pro-rated based on start date, in addition to sick time, paid holidays ...

Avient

Quality Associate

Avon Lake, OH

As a Quality Associate with Avient, you are responsible for testing product batches and will make ... Two weeks of vacation pro-rated based on start date, in addition to sick time, paid holidays ...

Superbeo

Supplier Quality Associate

Sturtevant, WI · On-site

Supplier Quality Associate Job Location: Sturtevant, WI 53177 Job Duration: 5 months Job Type ... Requirements: * BS/BA in Physical Science or Engineering or 2 + years in medical device ...

Baxter

Associate II, Quality (7pm-7am)

Marion, NC

Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices. Your Team at Baxter Within Quality ...

MSD

Bioanalytical Quality Associate

Gaithersburg, MD · On-site

$78K - $116K/yr

The Bioanalytical Quality Associate is responsible for verifying adherence to laboratory policies ... Training and experience in a Biosafety Level 2 (BSL-2) laboratory is preferred. KNOWLEDGE, SKILLS ...

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Quality Associate Ii information

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How much do quality associate ii jobs pay per hour?

As of Jun 30, 2026, the average hourly pay for quality associate ii in the United States is $26.93, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $31.49 per hour, depending on experience, location, and employer.

What is the difference between Quality Associate Ii vs Quality Control Technician?

AspectQuality Associate IIQuality Control Technician
Required CredentialsTypically an associate degree or higher in a related fieldOften an associate degree or technical certification
Work EnvironmentOffice and manufacturing settings, supporting quality processesLaboratory and production environments, performing testing and inspections
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and biotechPrimarily in manufacturing and production sectors
Search & Comparison IntentUnderstanding roles, responsibilities, and career pathFocus on testing procedures and technical skills

The main difference between a Quality Associate II and a Quality Control Technician lies in their focus and responsibilities. Quality Associate II roles often involve supporting quality systems, documentation, and process improvements, while Quality Control Technicians primarily perform testing and inspections to ensure product quality. Both roles require similar educational backgrounds but differ in daily tasks and work environments.

What are some typical challenges a Quality Associate II might face when working on cross-departmental projects?

As a Quality Associate II, you may frequently collaborate with teams from production, engineering, and regulatory affairs. One common challenge is ensuring clear communication and alignment on quality standards across departments, especially when project timelines are tight or priorities differ. You’ll often need to balance attention to detail with efficiency, managing documentation and compliance tasks while supporting process improvements. Developing strong working relationships and proactive communication skills can help you address these challenges effectively and contribute to smoother project execution.

What are Quality Associate IIs?

Quality Associate IIs are professionals who work in quality assurance or quality control, typically within manufacturing, pharmaceuticals, or other regulated industries. They are responsible for ensuring products and processes meet established standards and regulatory requirements. Their duties may include inspecting materials, reviewing documentation, conducting audits, and collaborating with other departments to resolve quality issues. Quality Associate IIs often have more experience than entry-level associates and may assist in training or supervising junior staff. Their work helps maintain product safety, consistency, and compliance.

What are the key skills and qualifications needed to thrive as a Quality Associate II, and why are they important?

To thrive as a Quality Associate II, you need a solid understanding of quality assurance processes, regulatory compliance, and technical documentation, often supported by a bachelor's degree in a scientific or technical field. Familiarity with quality management systems (QMS), statistical analysis tools, and industry-specific standards such as ISO or GMP is typically required. Strong attention to detail, analytical thinking, and effective communication skills set outstanding candidates apart. These abilities are crucial to ensuring product quality, regulatory adherence, and continuous process improvement in a highly regulated environment.
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What cities are hiring for Quality Associate Ii jobs? Cities with the most Quality Associate Ii job openings:
What are the most commonly searched types of Quality Ii jobs? The most popular types of Quality Ii jobs are:
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What job categories do people searching Quality Associate Ii jobs look for? The top searched job categories for Quality Associate Ii jobs are:
Quality Associate Ii jobs near you
Infographic showing various Quality Associate Ii job openings in the United States as of June 2026, with employment types broken down into 83% Full Time, 4% Part Time, and 13% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $56,018 per year, or $26.9 per hour.
Quality Associate

Quality Associate

Biocytogen

Waltham, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Job description

We are seeking a detail-oriented and motivated Quality Associate to join our team. In this role, you will support the day-to-day operations of our Quality Assurance (QA) and facility compliance programs within a non-GLP, research-focused environment. You will work closely with the QA team and scientific staff to ensure scientific rigor, data integrity, and high-quality deliverables for our clients.
Key Responsibilities:
  • 1. Document Control & Data Governance
    • Lifecycle Management: Assist in the administration of the Document Control system, including the formatting, routing, and version control of policies and SOPs.
    • Archiving: Manage the physical and digital QA archives. Ensure secure storage, accurate indexing, and controlled retrieval of raw data, completed study files, and logbooks.
  • 2. Quality Management Systems
    • Event Tracking: Assist in logging, tracking, and following up on Deviations, Corrective and Preventive Actions (CAPAs), and Change Controls to ensure investigations and facility modifications are properly documented and resolved within timelines.
    • Metrics Reporting: Periodically compile basic quality metrics (e.g., CAPA closure rates) to assist QA management in trend analysis.
  • 3. Compliance, Audit & Vendor Support
    • Audit Readiness: Support the preparation and hosting of external client audits (document retrieval, facility readiness) and participate in routine internal audits.
    • Vendor Qualification: Maintain the Approved Vendor List (AVL), track vendor qualification statuses, and assist in renewing quality agreements.
    • Client Inquiries: Assist in completing client quality questionnaires and ensuring sponsor expectations are met.
  • 4. Operations & Facility Oversight
    • Equipment & Training: Track laboratory equipment calibration/PM schedules and maintain personnel training matrices, ensuring scientists are up-to-date on required SOPs.
    • Sample Management & EHS: Monitor the receipt, storage, and dispensation of Test Articles (TA) to ensure chain of custody. Support routine EHS walk-throughs to maintain a safe laboratory environment.

Requirements
  • Education: Bachelor's or Master's degree in Biology, Bioengineering, Life Sciences, or a related field.
  • Experience: 0-2 years of experience in a laboratory, quality, or clinical setting (Industry internships or academic lab management experience are highly welcomed).
  • Quality Mindset: Basic understanding of Quality Systems (Deviations, CAPAs, Audits); familiar with GxP concepts is a plus.
  • Technical Savviness: High digital literacy and efficiency. Must be highly proficient in Microsoft Office Suite (Word formatting, Excel data management) and demonstrate the ability to quickly master new electronic tracking systems and document control software.
  • Work Style: A self-starter with a results-oriented approach. Must possess the ability to work independently, prioritize tasks efficiently, and deliver high-quality work without requiring constant micromanagement.
  • Communication: Excellent written and verbal communication skills, with the ability to collaborate effectively with cross-functional scientific teams.

Benefits
  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Health Reimbursement Accounts
  • Life and AD&D Insurance
  • Short & Long Term Disability Insurance
  • 401K with Company Match
  • Paid Time Off
  • Paid Sick Days & Holidays

BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one's qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

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