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Quality Assurance Reviewer Jobs (NOW HIRING)

Celularity Inc.

Lead, Quality Assurance

Florham Park, NJ · On-site

$90K - $115K/yr

Conducts QA review of product-related records, biobanking files, transplantation documentation, batch records, QC/environmental monitoring data, donor eligibility records, calibration records, and ...

CELULARITY LLC

Lead, Quality Assurance

Florham Park, NJ · On-site

$90K - $115K/yr

Conducts QA review of product-related records, biobanking files, transplantation documentation, batch records, QC/environmental monitoring data, donor eligibility records, calibration records, and ...

CityFirst Bank

Quality Assurance Analyst

Washington, DC · On-site

$87K - $92K/yr

This role supports quality assurance reviews, audit readiness, reporting and analytics process, improvement initiatives and business analysis functions. The QA Analyst ensures that loan files meet ...

MUFG Bank, Ltd.

Quality Assurance Analyst

Tempe, AZ · Hybrid

$71K - $89K/yr

The objectives of the routine reviews is to ensure of having a control process to determine whether process output adheres to established quality objectives and to provide reasonable assurance to ...

MUFG Bank, Ltd.

Quality Assurance Analyst

Jersey City, NJ · Hybrid

$71K - $89K/yr

The objectives of the routine reviews is to ensure of having a control process to determine whether process output adheres to established quality objectives and to provide reasonable assurance to ...

Integrated Resources INC

Quality Assurance

Groton, CT · On-site

Review supplier documentation to support the creation of material supply channels and ensure supply ... QA review and release of routine and high priority transfer/shipment requests and packaging and ...

PCI Pharma Services

Qa Associate I - Ops

Madison, WI · On-site

Quality Assurance Operations Supervisor Responsible For (Staff): No The Quality Associate I ... Review executed Manufacturing Batch Records and supporting documentation for completeness, accuracy ...

PCI Pharma Services

Qa Associate I - Ops

Madison, WI · On-site

Quality Assurance Operations Supervisor Responsible For (Staff): No The Quality Associate I ... Review executed Manufacturing Batch Records and supporting documentation for completeness ...

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How much do quality assurance reviewer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality assurance reviewer in the United States is $33.91, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $39.90 per hour, depending on experience, location, and employer.

What does a quality assurance reviewer do?

A Quality Assurance Reviewer evaluates products, services, or processes to ensure they meet established quality standards and compliance requirements. They analyze performance data, identify defects or inefficiencies, and recommend improvements. Their role may involve reviewing documentation, conducting audits, and providing feedback to teams to maintain consistency and enhance overall quality.

What are the key skills and qualifications needed to thrive as a quality assurance reviewer?

To excel as a Quality Assurance Reviewer, you should possess a keen attention to detail, strong analytical skills, and relevant experience in reviewing processes or documentation, often supported by a degree in a related field such as quality management or life sciences. Familiarity with quality management systems (QMS), auditing software, and certifications like Six Sigma or ISO 9001 can be valuable assets. Excellent communication, problem-solving, and time management skills help distinguish top candidates in this role. These capabilities ensure consistency, accuracy, and continual improvement in products or services, which are essential for organizational success.

What are the main challenges a quality assurance reviewer might face in their day-to-day work?

Quality Assurance Reviewers often encounter tight deadlines and must handle large volumes of data or documents while maintaining high accuracy standards. Balancing the need for thoroughness with operational efficiency can be challenging, especially when identifying and reporting subtle inconsistencies or non-conformities. Collaboration across multiple departments is common, requiring strong communication to align on quality standards and corrective actions. These challenges make the role dynamic and rewarding for those who enjoy detail-oriented and process-driven work environments.

How to become a quality assurance reviewer?

To become a quality assurance reviewer, candidates typically need a high school diploma or equivalent, with some roles requiring a bachelor's degree in a related field such as quality assurance, business, or healthcare. Relevant skills include attention to detail, strong communication, and familiarity with industry-specific tools or standards. Gaining experience through entry-level positions or certifications like Six Sigma can improve job prospects.
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Quality Assurance Reviewer jobs near you
Infographic showing various Quality Assurance Reviewer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $70,532 per year, or $33.9 per hour.

Lead, Quality Assurance

Florham Park, NJ • On-site

Celularity Inc.
Biotechnology Research and Development • 51 - 200 employees
Learn more about Celularity Inc.external

$90K - $115K/yr

Full-time

Posted 19 days ago

Job description

Job Type
Full-time
Description
About Celularity
Celularity Inc. (Nasdaq: CELU) is a longevity-focused regenerative and cellular medicine company developing and manufacturing allogeneic and autologous cell therapies derived from the postpartum placenta. Celularity leverages the placenta's unique biology, immunologic properties and scalable availability to develop therapeutic solutions targeting fundamental mechanisms of aging and age-related disease.
Purpose
The Lead, Quality Assurance (QA) is responsible for supporting clinical and commercial product quality through QA review of product-related records, batch documentation, QC and environmental monitoring data, donor eligibility records, and other quality documentation to support batch disposition and product release. This role also supports QMS processes, including controlled document review and approval, SOP periodic review, training assignments, and training compliance, while supporting change controls, investigations, OOS/OOT events, CAPA activities, audits, regulatory interactions and cross-functional QA guidance to maintain compliance with cGMP, GTP, applicable health authority regulations, and Celularity quality standards.
Role & Responsibilities
  • Conducts QA review of product-related records, biobanking files, transplantation documentation, batch records, QC/environmental monitoring data, donor eligibility records, calibration records, and validation documentation for completeness, accuracy, compliance, and applicable trends.
  • Reviews batch-related documentation, makes quality decisions supporting product release, performs batch disposition, and verifies completion of associated quality event activities.
  • Issues batch records and labels and conducts QA verification and reconciliation of product packaging and labeling.
  • Supports incoming materials inspection and release and resolves documentation errors or discrepancies with appropriate personnel.
  • Handles product-related quality events, including change controls, investigations, OOS/OOT events, CAPA coordination, follow-up, action-item tracking, and timely closure.
  • Writes, reviews, and approves SOPs and associated documents, including work procedures and forms, and provides input to improve processes and procedures.
  • Serves as a QA/QMS approver for controlled documents, including SOPs, work instructions, forms, and related procedural documents, ensuring appropriate review, approval, effectiveness, and alignment with applicable quality system requirements.
  • Supports administration of QMS processes such as document control, training assignments, periodic SOP reviews, and training compliance to maintain inspection readiness and procedural effectiveness.
  • Implements and ensures adherence to applicable Health Authority regulations, cGMP & GTP requirements, and Celularity quality standards.
  • Supports self-inspections, external audits, regulatory filings, and interactions with FDA, partners, and inspectors; serves as audit host as needed.
  • Provides day-to-day QA guidance to peers and cross-functional partners and serves as QA point of contact for assigned product or operational areas.
  • Completes job-related training in electronic database systems, GMP, safety, and Ethics & Compliance requirements.

Requirements
Minimum Qualifications (Must have)
  • Bachelor's degree in scientific discipline required.
  • Minimum of 5+ years of quality assurance experience in a cGMP-regulated environment.
  • Familiarity with cGMP and GTP environments
  • Ability to understand, follow, interpret and apply good laboratory practices.
  • Knowledge of OOS, OOT, investigation, and CAPA processes.
  • Strong organizational and time management skills
  • Ability to work well in a team environment
  • Dynamic individual with the ability to communicate and engage others
  • Independent and self-starting.
  • Eager and adaptable
  • Excellent verbal and written communication skills as well as strong focus and attention to detail.
  • Ability to don personal protective equipment (PPE) during various role responsibilities

Celularity Inc. is an equal opportunity employer
***THIS ROLE DOES NOT PROVIDE RELOCATION
***NO AGENCIES PLEASE
Salary Description
$90,000 - $115,000

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