Last updated: 2025-05-22

47 Quality Assurance And Engineering jobs in New York City.

Hiring now: Associate Dir Inspection @ Regeneron , Sr Mgr Gd Quality Managem @ Regeneron , Sr Associate Quality Eng @ L3Harris T, Regulatory Spec Fragrance @ Osmo, Dir Regulatory Cmc @ Eikon Ther, Vice President Innovative @ Johnson Jo, Cqv Eng Consultant @ Project Fa, Healthcare Quality Adviso @ Federal Ex, Sr Facilities Engr @ Genscriptp, Quality Systems It Mgr @ Legend Bio.Explore more at at kaamvaam.com

🔥 Skills

regulatory compliance (9) compliance (6) product development (6) project management (5) Corrective Action (5) cell therapy (5) cross-functional teams (5) cGMP (5) Quality Control (5) Documentation (5)

📍 Locations

New York City (17) Bridgewater (8) Basking Ridge (4) Somerset (4) Millburn (3) Clifton (2) Newark (2) Brooklyn (2) Elizabeth (1) Jersey City (1)
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Regeneron Pharmaceuticals Inc.

Associate Director Inspection Management (GCP) Basking Ridge
Skills & Focus: GCP, GVP, GLP, inspections, stakeholder engagement, regulatory compliance, quality management, clinical trials, training, risk mitigation
Experience: 10 years
Salary: $154,800.00 - $252,800.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Regeneron Pharmaceuticals

Senior Manager, GD Quality Management (GCP) Basking Ridge
Skills & Focus: Quality Management, GCP, compliance, clinical trials, risk management, stakeholders, audit, quality assurance, Corrective Action/Preventive Action, training
Experience: 8 years in healthcare/pharmaceutical industry
Salary: $132,400.00 - $216,000.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Regeneron Pharmaceuticals Inc.

Associate Director, GPS Standards & Training Basking Ridge
Skills & Focus: Pharmacovigilance, Drug Safety, Quality Management, Regulatory Affairs, Compliance, Project Management, Procedural Documentation, Training Compliance, Audits, Metrics
About the Company: Regeneron is a biotechnology company that develops and commercializes medicines for the treatment of serious medical conditions.
Experience: 7+ years in Pharmacovigilance/Drug Safety, Regulatory Affairs or Quality Assurance in the pharmaceutical/biotech industry
Salary: $154,800.00 - $252,800.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off
Senior Manager, Veeva Vault Clinical SSU Basking Ridge
Skills & Focus: Clinical Operations, GxP validation, Veeva Technology systems, Agile development, project management, vendor relationship management, customer experience, product support, continuous improvement, product strategy
Experience: 8+ years in Clinical Operations management
Salary: $132,400.00 - $216,000.00
Type: Contract
Benefits: Health and wellness programs, fitness centers, equity awards, annual bonuses, paid time off

L3harris Technologies

Senior Associate, Quality Engineering Clifton
Skills & Focus: Quality Assurance, Hardware, Electronic & Mechanical Spaceflight, Root Cause Analysis, Corrective Action, Quality Management System, ISO9001/AS9100, Process Audit, Continuous Improvement, Security Clearance
About the Company: L3Harris Technologies is a defense industry leader providing end-to-end technology solutions across air, land, sea, space, and cyber domains, dedicated to nati…
Experience: 4+ years supporting design, development, manufacturing, and/or quality engineering activities
Specialist, Quality Engineering Clifton
Skills & Focus: Quality Engineering, defect data analysis, corrective actions, quality system, manufacturing processes, non-conforming material, engineering design changes, defect dispositioning, material review board, cost of poor quality
About the Company: L3Harris is a defense industry leader providing technology solutions across air, land, sea, space, and cyber domains in the interest of national security.
Experience: Minimum 4 years of relevant experience; or 2 years with Graduate Degree; or 8 years without degree

Osmo

Regulatory Specialist, Fragrance Manufacturing Elizabeth
Skills & Focus: regulatory compliance, fragrance, SDS preparation, IFRA, REACH, FDA, EPA, technical documentation, product registrations, risk assessments
About the Company: Osmo is a digital olfaction company focused on enhancing human health and wellbeing through the power of smell.
Experience: Minimum of 3-5 years of experience in regulatory affairs
Type: Full time

Eikon Therapeutics

Director, Regulatory CMC Jersey City
Skills & Focus: Regulatory, CMC, pharmaceutical, biotech, regulatory affairs, compliance, drug targets, submissions, inspections, team management
About the Company: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biolog…
Experience: Minimum of 3 days a week onsite presence; 10+ years of experience in regulatory affairs, focusing on CMC aspects of pharmaceutical products.
Salary: $213,000 to $232,750
Type: Full-time
Benefits: 401k plan with company matching, Medical insurance (premiums covered at 95%), dental and vision insurance (100%), menta…

Johnson & Johnson

Vice President, Innovative Medicine Regulatory Compliance New Brunswick
Skills & Focus: regulatory compliance, FDA, inspection readiness, audit, leadership, supply chain, team culture, risk management, Good Manufacturing Practices, compliance excellence
About the Company: Johnson & Johnson is a leading global healthcare company that focuses on innovative medicine and medical technology, empowering health solutions and improving …
Experience: 15+ years working in US FDA regulated environments; 10+ years of people leadership
Type: Hybrid

Project Farma

CQV Engineering Consultant Newark
Skills & Focus: CQV Engineering, Technical Documentation, Project Management, Life Science, Validation Life Cycle, Mentoring, Business Development, Collaboration, Client Engagement, Fast-paced Environment
About the Company: Project Farma is the leading advanced therapy technical operations consulting company in the life science industry. They are committed to advancing manufacturi…
Experience: A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
Salary: $50,000 - $240,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance effective you…

Federal Express Corporation

Healthcare Quality Advisor-1 Newark
Skills & Focus: healthcare, quality assurance, management, project management, continuous improvement, business, transportation, logistics, supply chain, compliance
Experience: Five (5) years’ minimum experience required in healthcare quality
Salary: Indianapolis Pay Range: $6,511.62/month - $8,627.89/month; Newark Pay Range: $7,882.48/month - $10,444.28/month
Type: Full Time
Benefits: health, vision and dental insurance, retirement, and tuition reimbursement

Genscript/Probio

Sr. Facilities Engineer Piscataway
Skills & Focus: project management, biopharmaceuticals, facility operations, construction, validation, compliance, risk assessment, procurement, government permits, engineering
About the Company: GenScript Biotech Corporation is a global biotechnology group founded in 2002, specializing in gene synthesis technology, biopharmaceuticals, and cell therapy.…
Experience: 10+ years
Type: Full-time
Benefits: Competitive salary with performance-based bonuses, comprehensive health, dental and vision insurance, 401(k) retirement…

Legend Biotech

Quality Systems IT Manager Somerset
Skills & Focus: GxP, Validation, Veeva, Management, LMS, Compliance, IT Operations, Pharmaceutical, Quality Systems, Biotech
About the Company: Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inc…
Experience: 10+ years of hands-on experience in implementation and support of computerized systems in regulated GxP environment.
Sr. Data Manager Somerset
Skills & Focus: Clinical Data Management, Cell and Gene Therapy, CRO Oversight, Medidata Rave, Regulatory Compliance, Data Quality, Data Integrity, Clinical Trial, CDISC Standards, Project Management
Experience: Minimum of 10 years of clinical data management experience
Type: Full-time
Director, Regulatory CMC Somerset
Skills & Focus: regulatory, CMC, biotechnology, viral vector technology, global submissions, INDs, IMPDs, product development, regulatory guidelines, documentation
About the Company: Legend Biotech is a biotechnology company focused on developing innovative therapies for cancer and other serious diseases.
Experience: 10 years
Type: Full-time

Perrigo

Operations Supervisor The Bronx
Skills & Focus: Operations, Manufacturing, Leadership, Quality, Production, Team Development, Safety, Training, Problem-solving, FDA regulated
About the Company: Perrigo is a leading player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula products…
Experience: 4 years of leadership experience preferred
Salary: $85,000
Type: Full-time
Benefits: Competitive compensation, benefits tailored to supporting you and your family, career development opportunities.

Cresilon

Medical Device Engineer Brooklyn
Skills & Focus: medical devices, product development, design control, FDA Quality System Regulations, regulatory compliance, Solidworks, experimental design, user needs, Lean Six Sigma, biomedical engineering
About the Company: Cresilon® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company’s proprietary hyd…
Experience: A minimum of 4+ years of product development experience; at least 2 years in a cGMP-regulated industry
Salary: $80,000 - $160,000
Type: Full-time
Benefits: Competitive annual base salary range of $80,000 - $160,000, Paid Vacation, Sick, & Holidays, Monthly MetroCard Reimburs…
Medical Device R&D Project Manager Brooklyn
Skills & Focus: medical device, project management, biotechnology, product development, cross-functional teams, quality compliance, design control, PMP certification, risk management, innovation
About the Company: Cresilon® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company’s proprietary hyd…
Experience: A minimum of 6 years of technical project management experience in the medical device or biotechnology industry is REQUIRED; a minimum of 3 years in product development within the medical device industry is REQUIRED.
Salary: $100,000 - $160,000
Type: Full-time
Benefits: Competitive annual base salary range of $100,000 - $160,000, Paid Vacation, Sick, & Holidays, Medical, Dental, and Visi…

Parexel

Regulatory Affairs Jobs New York City
Skills & Focus: Regulatory Affairs, Consulting, Medical Device, Drug & Device Expert, Labeling Operations, Home Based, Functional Service Provider, Senior Regulatory Affairs Associate, East Coast, Remote

Baxter

Technical Services Jobs in New York New York City
Skills & Focus: Technical Services, medical devices, manufacturing, healthcare, patient care, medical solutions, product development, medical equipment, quality assurance, clinical support
About the Company: A healthcare company focused on manufacturing medical devices and solutions, dedicated to improving patient care and saving lives.
Type: Full-time

Formation Bio

Director, Medical Writing New York City
Skills & Focus: medical writing, clinical development, regulatory documents, pharmacovigilance, cross-functional teams, AI tools, Good Clinical Practice, document author, stylish guidelines, continuous improvement
About the Company: Formation Bio is a tech and AI driven pharma company focused on radically more efficient drug development, utilizing technology platforms and AI advancements t…
Experience: 7+ years in the development of clinical and regulatory documents
Salary: $250,000 - $300,000 for NYC and Boston; $238,000 - $285,000 for other eligible remote locations
Type: Hybrid
Benefits: Equity, generous perks, hybrid flexibility, comprehensive benefits

Intuitive Surgical

Head of Clinical Research Engineering New York City
Skills & Focus: clinical research, engineering leadership, medical devices, robotic systems, clinical studies, product development, regulatory compliance, patient safety, prototype evaluation, team management
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years in medical device development, 5+ years in leadership
Type: Full-time

Veeva Systems

Senior Director of Manufacturing & Quality Strategy New York City
Skills & Focus: Manufacturing, Quality Strategy, Biopharmaceuticals, Industry Cloud, Customer Solutions, Stakeholder Relationships, Customer Success, Digital Technologies, Thought Leadership, Adoption and Growth
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.
Experience: Senior leadership with a deep understanding of the global life sciences quality and manufacturing space and associated digital technologies.
Type: Full-time
Benefits: Flexibility to work from home or in the office, support for customer and employee success.

The Farmer's Dog

Packaging Engineer New York City
Skills & Focus: packaging engineering, sustainable packaging, food safety, CAD software, Lean Six Sigma, cross-functional teams, project management, packaging trials, consumer needs, regulatory compliance
About the Company: The Farmer’s Dog was born from a mission to change the landscape of pet health, providing dogs and their humans with honest, smart, and simple care. We’re star…
Experience: 3+ years in packaging engineering, preferably in the food industry
Salary: $70,000 - $85,000 USD Annual
Type: Full-time
Benefits: Comprehensive Healthcare, Dental, and Vision; Company supported mental health benefits; 12 week paid parental leave; Co…

Maesa

Senior Manager, Regulatory New York City
Skills & Focus: regulatory, compliance, safety standards, claims substantiation, product lifecycle, leadership, team development, domestic & global standards, cross-functional teams, regulatory guidance
About the Company: The next gen beauty company, Maesa is transforming the industry by incubating and growing meaningful, innovative brands and making prestige beauty accessible.
Experience: 6+ years
Salary: $110,000 - $130,000
Type: Hybrid
Benefits: Health insurance coverage, wellness programs, life and disability insurance, retirement savings plans, generous paid ti…

Formation Bio

Director, Quality Management Systems New York City
Skills & Focus: pharmaceutical quality systems, QMS, regulatory compliance, cGMP, quality assurance, internal and external audits, corrective and preventive actions, cross-functional collaboration, quality metrics, leadership
About the Company: Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. The company partners, acquires, or in-license…
Experience: 12+ years
Salary: $210,000 - $300,000
Type: Full-time
Benefits: Equity, generous perks, hybrid flexibility, comprehensive benefits.

Intuitive Surgical

Project Coordinator New York City
Skills & Focus: Project Management, Product Development, Cross-functional Collaboration, Risk Management, Design Control, Regulatory Submissions, Milestone Tracking, Quality Systems, Medical Devices, Process Improvement
About the Company: At Intuitive, we are committed to minimally invasive care through innovative robotic-assisted surgery technology. We foster an inclusive and diverse team dedic…

Selux

Manufacturing Engineer New York City
Skills & Focus: Manufacturing Engineer, Contract Manufacturing, cGMP, FDA guidelines, Product Development, NPI process, Validation and Verification, Good Manufacturing Processes, Supply Chain Management, Key Performance Indicators
About the Company: Selux’s mission is to preserve the lifesaving efficacy of antibiotics by providing diagnostic results in hours, rather than days. We are building a multidiscip…
Experience: 5+ years
Salary: $96K-$125K
Type: Part-time
Benefits: Competitive benefits package including healthcare, 401K match, stock option grants, open paid time off and supportive f…

Peloton

Sr. Engineer, Safety and Regulatory New York City
Skills & Focus: Product Safety, Regulatory Compliance, UL60335, ASTM, IEC, 3rd Party Certification, Chemical Regulations, Material Toxicity, Root Cause Analysis, Design & Quality Tools
About the Company: Peloton provides Members with expert instruction, and world class content to create impactful and entertaining workout experiences. Founded in 2012 and headqua…
Experience: Over 7 years in a product safety and regulatory role, experience in consumer goods/fitness equipment a plus.
Salary: $135,830—$183,370 USD
Type: Full-Time
Benefits: Medical, dental and vision insurance; Paid time off; Disability benefits; Mental health services; 401k; Tuition reimbur…

New York City Department Of Social Services

Principal Administrative Associate II New York City
Skills & Focus: Quality Control, Case Review, SNAP, Eligibility Criteria, Audit, Documentation, Corrective Action, Interviews, Federal QC, Regulations
About the Company: The DSS Accountability Office is responsible for protecting the integrity of social services programs administered by the New York City Department of Social Se…
Type: Full-time
Principal Administrative Associate II New York City
Skills & Focus: Quality Control, Case Review, SNAP, Eligibility Criteria, Audit, Documentation, Corrective Action, Interviews, Federal QC, Regulations
About the Company: The DSS Accountability Office is responsible for protecting the integrity of social services programs administered by the New York City Department of Social Se…
Type: Full-time
Principal Administrative Associate II New York City
Skills & Focus: Quality Control, Case Review, SNAP, Eligibility Criteria, Audit, Documentation, Corrective Action, Interviews, Federal QC, Regulations
About the Company: The DSS Accountability Office is responsible for protecting the integrity of social services programs administered by the New York City Department of Social Se…
Type: Full-time

Ro

Director of Packaging Development New York City
Skills & Focus: packaging engineering, user experience, cross-functional collaboration, strategic leadership, packaging design, patient-centric, regulatory compliance, scalability, automation, innovation
About the Company: Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possi…
Type: Full-time
Benefits: Recognized as a Fortune Best Workplace in New York and Health Care, Best Workplace for Parents, named in CNBC Disruptor…

Peloton

Sr. Program Manager - Product Safety/regulatory New York City
Skills & Focus: Product Safety, Regulatory Compliance, Consumer Goods, Certification, Test Procedures, Safety Standards, Investigation, Root Cause Analysis, Design Tools, Cross-Functional
About the Company: Peloton provides Members with expert instruction and world-class content to create impactful and entertaining workout experiences for anyone, anywhere and at a…
Experience: Over 7 years in a product safety and regulatory role
Salary: $135,830 - $183,370 USD
Benefits: Comprehensive benefits including health insurance, paid time off, disability, mental health services, 401k, tuition rei…

Novartis

QA Operations Specialist Millburn
Skills & Focus: Quality, GxP compliance, batch record review, product release, CAPAs, Deviations, change controls, regulatory inspections, cGMP, continuous quality improvement
About the Company: Novartis is an innovative medicines company working to reimagine medicine to improve and extend people's lives. They focus on a wide range of therapeutic areas…
Manufacturing Head, Millburn Site Millburn
Skills & Focus: manufacturing, GMP, radioligand therapy, supply chain, quality, safety, leadership, compliance, capex, operations
About the Company: Novartis is an innovative medicines company focused on reimagining medicine to improve and extend people's lives. They work across various therapeutic areas in…
Process Expert Millburn
Skills & Focus: nuclear medicine, targeted radioligand therapy, manufacturing, technical support, process expert, deviation investigations, CAPA, data analysis, quality requirements, team management
About the Company: Novartis is an innovative medicines company that works to improve and extend people's lives through advanced medical treatments and therapies.
Type: Full-time

Cellares

QC LIMS Administrator Bridgewater
Skills & Focus: QC, LIMS, administrator, cell therapy, GMP, regulatory, data integrity, report design, training, stakeholder collaboration

Cellares

Computer System Validation (CSV) Engineer Bridgewater
Skills & Focus: Quality Engineering, FDA-regulated environment, cGMP, GAMP 5, multidisciplinary, product life cycle, product development, production builds, market release, fast-paced environment
About the Company: Cellares is focused on advanced cell therapy manufacturing.
Principal Enterprise Architect, GMP Systems Bridgewater
Skills & Focus: Enterprise Architect, GMP Systems, cell therapy, manufacturing facility, IDMO IT strategy, infrastructure development, planning, design, implementation, coordination
About the Company: Cellares is focused on developing innovative cell therapy solutions.
Sr. Product Manager - Cell Therapy Manufacturing Bridgewater
Skills & Focus: cell therapy, manufacturing, automation, product management, biotech, biologics, cell culture, scale-up, manufacturing processes, cross-functional
About the Company: Cellares is developing integrated technologies for cell therapy manufacturing, including the Cell Shuttle platform, to accelerate access to life-saving cell th…
Experience: 5+ years of product management experience in biotech or medical devices
Salary: $90,000 - $210,000 a year
Type: Full-time
Benefits: Medical, Dental, Vision, 401(k), Stock options, Onsite lunches, EV charging

Bausch Health

Director, Regulatory Affairs (Global Labeling) Bridgewater
Skills & Focus: labeling, regulatory affairs, drug products, guidance, strategic development, cross-functional teams, labeling documents, health authority interactions, risk assessment, medical concepts
About the Company: Bausch Health is a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufa…
Experience: 8+ years of relevant experience in pharmaceutical labeling/regulatory experience.
Benefits: Comprehensive Medical (includes Prescription Drug), Dental, Vision, Health Savings Account with company contribution, F…
Senior Regulatory Affairs Specialist Bridgewater
Skills & Focus: Regulatory Strategy, Compliance, Documentation, Product Development, International Submissions, Analytical Reasoning, Communication Skills, Interpersonal Skills, Risk Management, Pharmaceutical Industry
About the Company: We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufacture and …
Experience: 2+ years of relevant pharmaceutical industry and regulatory experience; brand experience preferred
Benefits: Comprehensive Medical (includes Prescription Drug), Dental, Vision, Health Savings Account with company contribution, F…