500 Results for

Quality Assurance Specialist Jobs in New Jersey

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New!

Totowa, NJ3 days ago

p> Ensure that components, containers, closures, in-process materials, packaging materials, labeling, and finished dosage forms are examined and approved or rejected to ensure that all these meet their current specifications.

Maintain oversight of the QA program and Quality Management System (QMS) at a single SOFIE manufacturing facility producing products under both 21 CFR Part 212 and 211 (as needed) regulations.

New!

South Brunswick, NJ6 days ago

$31–$35 Per Hour

li> Evaluate deviations, investigations, change controls, out-of-specification (OOS) and out-of-trend (OOT) events, and CAPA activities, including root cause analysis and quality impact assessments. Required Experience/Skills for the QA Data Review & Compliance Specialist:

3 - 5 years of experience in Quality Assurance, Quality Systems, Compliance, Auditing, or Data Review within a pharmaceutical, biotechnology, or regulated life sciences environment.

Totowa, NJ27 days ago

li class="MsoNormal" style="background-color:white;color:black;line-height:13.5pt;margin-bottom:0in;margin-right:0px;margin-top:0px;padding:0px">Ability to effectively present information, deliver training, and respond to questions from groups of managers, clients, customers, and the general public required.

Identify and assess the training needs of the organization through job analysis, knowledge gaps, operational analysis, and consultation with other SOFIE network leadership.

Totowa, NJ27 days ago

Identify and assess the training needs of the organization through job analysis, knowledge gaps, operational analysis, and consultation with other SOFIE network leadership.

Livingston, NJ30+ days ago

$90,000–$115,000 Per Year

p>Job Summary:

The Life Science Quality Assurance Specialist III is primarily responsible for establishing, developing, implementing, maintaining and improving Quality System processes and programs to include: Quality Event Reporting (Deviations, Nonconformance, Change Management, CAPA, Complaint), Document Control Program, Supplier Qualification, Validations, and Product Transfer. The candidate should have strong written and verbal communication skills to foster cross-functional collaboration and partnerships, lead by positive influence, maintain a high level of integrity, and possess a strong continuous improvement mindset.

Edison, New Jersey30+ days ago

div>One of the Best Clinical Trial Supply Leaders

JRS is one of the leading in sourcing and management of quality, certified, commercially available medicines (comparators, concomitant medication, rescue medication) for clinical trials.

The Quality Assurance Specialist – Clinical Trial Supply plays a critical role in ensuring the quality, safety, integrity, and compliance of clinical trial materials throughout their lifecycle—from receipt and storage to packaging, labeling, distribution, and returns.

Camden, NJ21 days ago

The role of the Quality Assurance Specialist is to assist and support the Director, Quality Assurance in fulfillment of all quality assurance job-related responsibilities including but not necessarily limited to ensuring the efficiency, effectiveness and economy of the internal control systems and processes. Rewards & Benefits: We know Michaels' promise of lifting lives starts with our teammates, so making sure every single teammate is happy, healthy, and set up for a successful future is important to us.

New!

Camden, NJ5 days ago

$60,000–$65,000 Per Year

p>The role of the Quality Assurance Specialist is to assist and support the Director, Quality Assurance in fulfillment of all quality assurance job-related responsibilities including but not necessarily limited to ensuring the efficiency, effectiveness and economy of the internal control systems and processes.

Rewards & Benefits:

We know Michaels' promise of lifting lives starts with our teammates, so making sure every single teammate is happy, healthy, and set up for a successful future is important to us.

Camden, New Jersey22 days ago

$60,000–$65,000 Per Year

The role of the Quality Assurance Specialist is to assist and support the Director, Quality Assurance in fulfillment of all quality assurance job-related responsibilities including but not necessarily limited to ensuring the efficiency, effectiveness and economy of the internal control systems and processes. We know Michaels’ promise of lifting lives starts with our teammates, so making sure every single teammate is happy, healthy, and set up for a successful future is important to us.

NJ13 days ago

$105,000–$150,000 Per Year

li>Perform accurate mechanical, physical, and visual inspections, conduct process surveillance through witnessing and monitoring techniques, and verify test results and documentation for raw materials, components, and sub-assemblies in accordance with approved inspection documents and specification requirements.

Execute quality requirements in accordance with customer-approved quality assurance plans, policies, and specifications during all phases of hardware fabrication, testing, first article inspections, and final end-item inspections.

Springfield, NJ13 days ago

$105,000–$150,000 Per Year

Perform accurate mechanical, physical, and visual inspections, conduct process surveillance through witnessing and monitoring techniques, and verify test results and documentation for raw materials, components, and sub-assemblies in accordance with approved inspection documents and specification requirements. Execute quality requirements in accordance with customer-approved quality assurance plans, policies, and specifications during all phases of hardware fabrication, testing, first article inspections, and final end-item inspections.

NJ8 days ago

$25.50–$35.53 Per Hour

li>Works in accordance with area Supervision to provide quality assurance oversight where the business is responsible for adhering to current Good Manufacturing Practices (cGMPs) including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review, batch disposition, and product distribution as applicable. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation.

Lawrenceville, NJ30+ days ago

$81.05–$85.96 Per Hour
Full-time
Employee

Position Overview:This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area. Maintain close communication with stakeholders and team members to keep apprised of CSV needs, interpretation of requirements, impacts on compliance of an application, project status, and other relevant issues.

Cranbury, NJ30+ days ago

$60,200–$96,300 Per Year

Qualifications: • Bachelors/Masters in relevant field (e.g., Life Sciences, Pharmacy) • 1-2 years in QA/project management, preferably in pharma/biotech • GMP regulations, project management methodologies • Strong communication, problem-solving, and organizational skills • Tools such as Project management: Jira, Aspera, MS Project, Document control: SharePoint, Document Vault (any skill would be a plus). Responsibilities: • Oversee QA projects, ensuring timely completion and quality • Coordinate cross-functional teams (QC, Regulatory and other relevant departments etc.) • Develop and execute project plans, timelines • Ensure compliance with GMP, regulatory requirements • Identify and mitigate project risks, track progress • Collaborate with stakeholders on project scope, changes.

Lawrence Township, NJ24 days ago

$77.14–$81.81 Per Hour
Full-time
Employee

The Production Manager works closely with various external agency partners, including creative and production agencies, to ensure seamless workflow, asset creation, and on-time delivery of marketing materials. The Production Manager partners with external agencies and internal matrix teams to oversee projects, ensure deadlines are met, and support continuous optimization of operational models.

Boulder, CO, CO22 days ago

Full-time

Additional Job Details: The Product Testing Engineer Softgoods is responsible for planning, executing, and documenting product validation, quality inspections, and compliance testing across the softgoods development and manufacturing lifecycle. Tanisha Systems services clients in Government, Banking & Financial Markets, Insurance, Healthcare, Retail & Consumer Goods, Energy & Utilities, Life Sciences, Telecom, Manufacturing and Transportation Industries around the globe.

Florence, NJ19 days ago

As a vital part of the receiving department, the warehouse receiving quality assurance specialist inspects the merchandise to ensure B&H has received what it was supposed to receive and in perfect condition. Long known as "The Professional's Source", B&H is recognized by savvy consumers worldwide for its honest, knowledgeable guidance, expert tips and articles… and always-great prices.

Edison, NJ30+ days ago

The Quality Assurance Specialist – Clinical Trial Supply plays a critical role in ensuring the quality, safety, integrity, and compliance of clinical trial materials throughout their lifecycle—from receipt and storage to packaging, labeling, distribution, and returns. The QA Specialist ensures that all products and processes meet regulatory and customer expectations while supporting JRS’s mission to deliver reliable, resilient, and high-quality clinical supply solutions worldwide.

Fords, NJ30+ days ago

$74,500–$109,200 Per Year

LANXESS has achieved leading positions in the Dow Jones Best-in-Class Index and the MSCI ESG and ISS ESG ratings, among others, for its commitment to sustainability. We are seeking a range of human interests, backgrounds, and experiences that can be engaged to achieve respect, ownership, trust, professionalism, integrity and healing across all sectors.

Bridgewater, NJ22 days ago

$38–$40 Per Hour

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. This position offers an excellent opportunity to gain well-rounded experience across quality operations, documentation, and floor oversight-particularly within advanced therapeutic manufacturing.

Princeton, New Jersey14 days ago

p>You will work on a variety of projects with several different styles of training, primarily interactive media such as eLearning, instructor-led courses/workshops, videos, and print resources. For these materials, within the constraints of our/clients’ guidelines, you will:

Copyedit assets created by subject matter experts or instructional designers during various project life cycles.

Monroe Township, New Jersey30+ days ago

$50,000–$60,000 Per Year

System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. Utilize available data to aid in continuous improvement efforts related to food safety and quality in production, maintenance, sanitation, and quality assurance areas.

New!

NJ5 days ago

p>Job Summary: The Proofreader/QA Specialist role is responsible for ensuring all marketing and brand materials, across print and digital, are accurate, polished, and error-free before release.

Knowledge, Skills, and Abilities:

Well-developed ability to multi-task and prioritize, strong organizational skills, detail orientation and accuracy are of the highest importance.

New Brunswick, NJ30+ days ago

$40.70–$43.18 Per Hour
Full-time
Employee

The incumbent partners closely with crossfunctional stakeholders including laboratory teams, project managers, external vendors, and Quality Assurance to ensure clear communication, alignment to business priorities, and timely execution of deliverables supporting clinical and commercial programs. Success in this role requires the ability to operate effectively in a fastpaced, matrixed environment with changing priorities, demonstrate strong attention to detail and data integrity, and contribute to continuous improvement of processes, systems, and team culture through collaboration, accountability, and adherence to Client values.

Fairfield, NJ30+ days ago

Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Ensures process nonconformances (PNC), deviations, change controls, and other Quality Assurance tools are appropriately completed and tracked.

Fairfield, NJ30+ days ago

Provides support to technical staff in their efforts to ensure that routine testing submitted by clients is completed within established parameters governing turnaround time, quality specifications, etc. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

New Brunswick, NJ27 days ago

Corp., a division of Spectrum Laboratory Products, Inc., has grown into the chemical industry's leading customer-focused global supplier of high quality chemicals, laboratory supplies and equipment. The California and New Jersey plants are also FDA registered drug establishments and operate under current Good Manufacturing Practices (cGMP).

OLD BRIDGE, New Jersey30+ days ago

$57,500–$83,400 Per Year

td>

Minimum of 2 years of related quality assurance,

service delivery, or field operations experience.

Prior experience in service-based industries such

as sanitation, logistics, or facilities preferred.

TWIC Card and other site-specific safety

certifications (as needed based on customer/site

access requirements)

Newark, NJ30+ days ago

$22–$24 Per Hour

Main Duties and Responsibilities: Conducts temperature checks on products and ensures that all HAPPC, and FDA rules and regulations are followed along with managing the units log books. This position is responsible for the oversight of all HACCP logs in the Hot Foods Production ensuring that the logs are completed as per company policies and procedures.

Pennsauken, NJ30+ days ago

To ensure products satisfy the required quality levels and that operations are consistently efficient and effective, employees must wear protective clothing such as a uniform, coverall, frock, hair net, beard cover, etc. in certain areas of the facility. This position also requires some standing, pulling (e.g., files, boxes, or binders from shelves, filing cabinet or carts), fingering (computer keyboard), grasping (computer mouse, talking, and hearing.

Pennsville, New Jersey30+ days ago

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Your Role: .

A BA/BS degree in microbiology, biology, chemistry, or engineering and 3-5 years of experience in QA in a pharmaceutical manufacturing environment , or an equivalent combination of education and experience.

Pennsville, NJ30+ days ago

$82,000–$110,000 Per Year

EDUCATION AND EXPERIENCE: A BA/BS degree in microbiology, biology, chemistry, or engineering and 3-5 years of experience in QA in a pharmaceutical manufacturing environment required, or an equivalent combination of education and experience. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide.

New!

Totowa, NJ6 days ago

p>Ensure that components, containers, closures, in-process materials, packaging materials, labeling, and finished dosage forms are examined and approved or rejected to ensure that all these meet their current specifications.

Maintain oversight of the QA program and Quality Management System (QMS) at a single SOFIE manufacturing facility producing products under both 21 CFR Part 212 and 211 (as needed) regulations.

Cranbury, NJ20 days ago

$63,000–$93,000 Per Year

The ideal candidate is a detail-oriented quality professional with a degree in Food Science, chemistry, or a related life science and at least three years of quality assurance experience, ideally within the food or dietary supplement industry. The benefits set forth in this posting reflect Innophos' current benefits for similarly situated employees, are subject in all respects to the terms and conditions of the applicable program policies and may be modified or discontinued by Innophos in the future (subject to applicable law).

Newark, NJ30+ days ago

p>Hologic is seeking a Director of Design Assurance to lead quality strategy for a high‑visibility portfolio within our Breast & Skeletal Health division. At Hologic, we are seeking a Product Quality Engineer 2 to provide engineering support for on-market medical devices.

NJ10 days ago

$106,200–$167,200 Per Year

p>Required Skills:

Analytical Thinking, Audits Compliance, Clinical Research, Clinical Trials, Detail-Oriented, Ethical Compliance, GCP Auditing, Investigative Skills, Metrics Analysis, Multiple Therapeutic Areas, Process Improvements, Stakeholder Management, Taking Ownership, Technical Documentation Management, Time Management.

Our Research Laboratories Quality Assurance (QA) is an independent organization that provides quality focus at each critical stage of the product development life cycle, including post approval marketing, to ensure high-quality, safe, and effective products, contributing to the company mission of improving and saving lives around the world.

Cranbury, New Jersey23 days ago

$63,000–$93,000 Per Year

div>The benefits set forth in this posting reflect Innophos’ current benefits for similarly situated employees, are subject in all respects to the terms and conditions of the applicable program policies and may be modified or discontinued by Innophos in the future (subject to applicable law).

$63,000 - $93,000 a year

The actual salary paid to an individual will vary based on multiple factors, including but not limited to education, specific skills, licenses and certifications, experience, and training.

About Innophos

Innophos is a leading international producer of specialty ingredient solutions that deliver far-reaching, versatile benefits for the food, health, nutrition and industrial markets. The Quality Assurance Documentation Specialist will assist in developing, facilitating and continually improving the Supplier Quality (SQ) Documentation Processes, focusing on the Supplier Documentation requirements from a quality or regulatory standpoint.

Belvidere, NJ30+ days ago

$66,000–$80,000 Per Year

Computing skills in Microsoft programs (Word, Excel, PowerPoint, Outlook, Teams) are required; experience with SAP, TrackWise, EDM and Mendix tools (e.g., iCCR) is preferred. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.

New Brunswick, NJ29 days ago

$78,980–$95,708 Per Year

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Mount Laurel, NJ28 days ago

$91,000–$136,240 Per Year

Job Description: The Centralized Governance & Control - Remediation Quality Assurance Testing team performs in-flight Assurance Testing Activities throughout the Issue Remediation Lifecycle to ensure Management Action Plans (MAPs) are designed to sufficiently mitigate and manage risk drivers of the issues and operate effectively. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition.

Ledgewood, NJ30+ days ago

Members of our Harrow Family often express their pride in being a part of our commitment to (1) innovation, (2) patient access to affordable medicines, and (3) our track record of having never turned down an ophthalmologist doing mission work around the world - providing free medicines in support of mission work aimed at giving or maintaining the gift of sight to those most in need. Management includes the periodic review of in-process activities such as cleaning, weighing, aseptic filling, material status verification, compounding, batch record documentation accuracy, logbook documentation accuracy, and room/line clearances.

Wall, NJ30+ days ago

This role is responsible for monitoring and evaluating agent performance, identifying areas for improvement, and providing constructive feedback to enhance the quality, consistency, and professionalism of customer-agent interactions. Required Skills/Abilities: Excellent Communication Skills: Strong written and verbal communication skills, able to provide constructive feedback in a clear and supportive manner.

New!

Monmouth Junction, NJ2 days ago

Also requires skills (2 yrs exp) in: cGMPs in the pharmaceutical industry; Issuing, tracking and closing Investigations, CAPAs, CPIs, Planned Deviations and Product Quality Complaint Investigations; conducting investigations leading to root cause and closure of investigations within defined timelines; conducting investigations, root cause analysis, CAPA or CPI in accordance with Quality System; and tracking and trending quality metrics for open Investigations: lab OOS/OOT/Lab Event, CAPAs/CPIs, planned deviations, and product quality complaints. ### Experience Required 2 years ### Minimum Education Required Bachelors ### Compensation $81,037.00 - $81,037.00 / Yearly ### Hours Per Week 40 ### Number Of Positions 1 ### Job Description Specialist I, QA QMS for Tris Pharma, Inc to work at our Monmouth Junction, NJ loc.

East Hanover, NJ30+ days ago

$89,600–$166,400 Per Year

p>Cross Train Expectations:

• QA Batch Release: • Perform Master Batch Record approvals and issuance of batch records and labels • Reviewing and approving raw material documentation and supplier CoAs to ensure quality and compliance of raw materials to be used in manufacturing processes • Perform Final Batch Record Review and Final Product Release • Perform a comprehensive review of all executed batch records and associated documentation to ensure compliance with specifications and regulatory requirements before product release.

• QA Compliance: • Support the following programs as needed: Change Control Management, Customer Complaint Management, Document Control Management, Training Program Management, Supplier Qualification Program, Audit/Self-Inspection Program, Annual Product Quality Review (APQR), Logbook Issuance.

NJ8 days ago

Pennsauken, NJ27 days ago

East Brunswick, NJ30+ days ago

This role requires a combination of office-based work and field visits to residential program . Assurance Specialist will also assist in monitoring program operations to promote ongoing .

Princeton, NJ30+ days ago

$130,000–$160,000 Per Year

Strong written and verbal communication skills in English, with the ability to work cross‑functionally under tight timelines, manage multiple priorities with high attention to detail, and willingness to successfully complete required visual acuity testing (including Graham Field Eye Test Chart and Ishihara Color Vision Test). Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.

Egg Harbor Township, NJ30+ days ago

$65,650–$118,675 Per Year

The Leidos National Airspace Systems Integration Support (NISC) Program is looking for a part-time Quality Assurance Specialist to support the Federal Aviation Administration's (FAA) William J. Hughes Technical Center for Advanced Aerospace in Atlantic City, New Jersey. For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.

07054, New Jersey30+ days ago

Review and assess supplier-provided technical documents for raw materials and finished goods, including SDSs, specifications, allergen/GMO statements, BSE/TSE letters, nutritional data, test methods, certifications, and SIDIs. System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.

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Quality Assurance Specialist Jobs in New Jersey

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Product Testing Engineer / Product Testing Specialist – Softgoods Tanisha Systems

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Quality Assurance Documentation Specialist - Supplier Quality Innophos Holdings Inc

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Quality Assurance Documentation Specialist – Supplier Quality Innophos

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