QMS jobs in Remote

Normal, Illinois

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Today

About Rivian Rivian is on a mission to keep the world adventurous forever. This goes for the emissions-free Electric Adventure Vehicles we build, and the curious, courageous souls we seek to attract. As a company, we constantly challenge what's possible, never simply accepting what has always been done. We reframe old problems, seek new solutions and operate comfortably in areas that are unknown. Our backgrounds are diverse, but our team shares a love of the outdoors and a desire to protect it

Full-time

USD 98,500.00 - 123,100.00 per year

QMS Analyst

Burlingame, California

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Today

Job#: 3045579 Job Description: Apex Systems is seeking a Quality System Analyst to support a clients Hearing Enhancement and wearable technology programs. This role will focus on post-market surveillance (PMS), complaint investigations, and customer quality activities supporting regulated products. The ideal candidate will have experience handling product complaints, conducting root cause investigations, supporting CAPA activities, and working within a Quality Management System in a regulated en

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Full-time

$35 - $45 per hour

QMS Business System Analyst (ComplianceQuest)

Irvine, California

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Today

No Corp-to-corp. No 3rd party firms . Position: QMS Business System Analyst (ComplianceQuest) Location: 4-day onsite in Irvine, CA (Only local candidates will be considered) Terms: Direct-hire Compensation: $130,000 to $165,000 + benefits . About the Role We are partnered with a client seeking an experienced Business Systems Analyst (QMS) to lead the support, enhancement, and optimization of our enterprise Quality Management System powered by ComplianceQuest on the Salesforce Platform. T

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Full-time

$130000 - $165000 per annum

QMS Audit Manager - EHSS

South Hackensack, New Jersey

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11d ago

Amtex SystemsInc is an information technology and talent solutions company offering talent and BI consulting to the companies in US for over 25 years. Our solutions are designed to fill resource gaps, by providing the right candidates who deliver value to the organization. Our propensity to nurture and build strong relationships with our clients helps us better understand their business demands and gives us the ability to provide services that are on time and rise above the rest. QMS Audit Manag

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Full-time, Third Party

$150000 - $165000

Veeva QMS

Remote

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2d ago

Job title: Veeva QMS Location: Remote Duration: 6 months plus with possible extension Role Descriptions: 1. Veeva QMS 2. Good understanding of Quality processes, including Deviations, CAPA, Lab Investigations, Change Control, Audits, Complaints, and Training. 3. Application Support (Incident, Problem, Change Management) 4. Excellent stakeholder management and communication skills with the ability to interact effectively with business and technical teams. Good-to-Have 1. Work Experience in Pharma

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Contract

CAPA/QMS Quality Engineer (On-Site)(No Corp to Corp or H-1B)

Pacheco, California

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2d ago

Please note that this is a 12-18 Month Contract and is On-Site. No Corp to Corp or H-1B. JOB DESCRIPTION: Education: Science or Engineering: BS/MS/PhD or equivalent industry experience Required Experience: Minimum 5 years working in a Quality Engineer role in a regulated industry and experience interfacing with regulatory bodies Strong knowledge of quality management systems, including but not limited to ISO standards, GxP, and QSR Operations or Quality Experience in Medical Device Manufactur

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Contract

Depends on Experience

Veeva Vault Regulatory Product Owner

Hybrid in Trenton, New Jersey

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3d ago

Job title: Veeva Vault Regulatory Product Owner Location: Ewing, NJ Work Arrangement: Hybrid Onsite 3 days a week Local Candidates: Required Job Summary We are seeking a Technical Product Owner to lead the strategy, roadmap, and delivery of digital solutions supporting Product Lifecycle Management (PLM), Quality Management Systems (QMS), and Regulatory processes across global R&D. This role combines product ownership with business analysis, partnering with stakeholders and technical t

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Contract, Third Party

Depends on Experience

Principal Quality Systems Engineer, QMS - Alpharetta, GA

Alpharetta, Georgia

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Today

Requisition ID:7180 Job Title:Principal Quality Systems Engineer, QMS - Alpharetta, GA Job Country:United States (US) Here at Avanos Medical, we passionately believe in three things: Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do; Making a difference in how we work and collaborate, constantly nurturing our nimble culture of innovation; Having an impact on the healthcare challenges we all face, and the lives of peo

Full-time

QMS Engineer

Cleveland, Ohio

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Today

Quality isn't just a department at PPG - it's a culture. As a QMS Engineer, you won't just maintain systems; you'll drive transformation. Your work will directly influence how products are made, tested, and delivered to customers across the globe. You'll be a champion of consistency, a solver of complex problems, and a key enabler of PPG's growth strategy. What You'll Do Own the QMS - Design, implement, and continuously improve quality management systems that set the standard for operational exc

Full-time

USD 110,000.00 - 115,000.00 per year

Validation Engineer

Hybrid in Chicago, Illinois

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3d ago

QUALITY ENGINEER / QUALITY COMPLIANCE ENGINEER our client is looking to hire 15-20 people Will provide cross-divisional support for remediation efforts. Under broad supervision, responsible for independently setting and upholding quality standards for portfolio of medical device, commodity, OTC drug, and/or cosmetic products. Evaluate production process, recommend improvements, qualify and conduct vendor management, generate and maintain DMRs, product specifications, design control files, and CE

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Contract

Depends on Experience

Quality Management System Engineer

East Brunswick, New Jersey

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26d ago

Job description:- Quality Management System Engineer Position - 1 Location - Santa Clara, CA Fulltime Experience : 8+ Job Description Summary: 1. Experience in Quality Management Systems(QMS), ISO9001, Change Management and Material Review Boards(MRB) 2. Hands-on experience in Supplier Product Change Notification (PCN) Management 3. Able to manage and deliver projects independently. 4. Excellent communication and interpersonal skills Detailed Job Responsibilities Manage Supplier PCN Process En

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Full-time, Third Party

$140000

Quality Manager

South Hackensack, New Jersey

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11d ago

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Full-time, Third Party

Depends on Experience

Supply Chain Specialist (Pharma/Biotech)

Santa Monica, California

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9d ago

About Nexinfo NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. We offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. We aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Our ERP-related services address challenges such as inven

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Contract, Third Party

$70 - $80

Auditor

Remote or Chicago, Illinois

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Today

Job Title: Quality Auditor Locations: Remote (50 - 60% Travel is expected anywhere in US but that will be sponsored) Duration: 6 months Contract Pay Range: $40 - $43/hr. Must Have's 8+ years of Quality Assurance and Quality Auditing experience within the medical device or pharmaceutical industry Extensive experience leading supplier/vendor audits from planning through final reporting Expert knowledge of FDA regulations (21 CFR Parts 210, 211, and 803), ISO 13485, and Quality Management Systems

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Full-time

$40.0000 - $43.0000

Mold Validation Engineer

Minneapolis, Minnesota

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Today

Primary Responsibilities: Executes mold trials (Functional Test, Gate Freeze, D3, Characterization) Captures RJG data & defines validated process windows Updates PODs & FW redlines Prepares draft OQ/PQ plans Coordinates daily with Healthcare ME, Ops, Quality, and Tooling pproves POD redlines & validation documents Ensures compliance with QMS & regulatory standards Run trials, collect RJG data, set process windows Prepare PODs, FW redlines, OQ/PQ drafts Coordinate with Healthcare teams Define mol

Full-time

Quality manger

Hybrid in Crystal Lake, Illinois

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12d ago

Role Summary We are seeking an experienced Quality Manager for a manufacturing facility based in Crystal Lake. This role reports directly to the Plant Manager and is responsible for leading the sites Quality Management System, ensuring compliance with ISO standards, and driving continuous improvement across all quality-related functions. The ideal candidate is a hands-on quality leader who can balance strategic oversight with operational execution while building a strong quality culture across t

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Full-time

90,000 - 100,000

Associate Scientist III – Analytical Development & Quality Control

New Haven, Connecticut

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3d ago

We are seeking an Associate Scientist to support analytical development and quality control activities for biological products across clinical and commercial programs. This role will collaborate with internal and external laboratories to support assay performance, analytical testing, data trending, method validation/transfer, and quality investigations. QualificationsBachelors or Masters degree in Chemistry, Biochemistry, Molecular Biology, Cell Biology, or related field.36+ years of analytical

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Contract

45 - 48

GxP Project Manager (Pharma)

Hybrid in San Francisco, California

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4d ago

Job Title: GxP Project Manager Location: Bay Area, CA Duration: 6+ months with possible of extension Required Qualifications Bachelor's degree in Engineering, Computer Science, Life Sciences, Pharmacy, Biotechnology, or related field.8+ years of Project Management experience within the Pharmaceutical or Biotechnology industry.5+ years managing GxP-regulated projects.Strong understanding of GMP, GxP, GAMP 5, FDA regulations, and 21 CFR Part 11.Experience managing Computer System Validation (CSV)

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Contract, Third Party

$80 - $90

Validation Engineer

Portsmouth, New Hampshire

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Today

Job Description: The CSV Specialist Level 4 provides team leadership and training to assess new and changing computer systems to ensure compliance with company policies, procedures and industry guidance. The CSV Specialist Level 4 will risk assess systems, review change requests and test scripts, draft protocols and initiate and review GMP documentation revisions. Specialist will be involved as the QA CSV representative during small and large-scale projects. Responsibilities: Perform all aspect

Full-time

Quality Assurance Analyst

No location provided

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Today

Job ID: 2615537 Location: , , US Date Posted: 2026-08-12 Category: Quality Assurance Subcategory: Qual Assurance Schedule: Full-Time Shift: Day Job Travel: No Minimum Clearance Required: None Clearance Level Must Be Able to Obtain: Public Trust Potential for Remote Work: ORA_REMOTE Description We are seeking an experienced Quality Assurance Analyst to support the nationwide deployment, installation, testing, and sustainment of the Tower Simulation System program. The Quality Assurance

Full-time