Remote QA & Compliance Specialist (Medical Devices)
Alcon Pharma
Location: New York, United StatesCompany: AlconPosted: 2026-10-19Alcon in the United States seeks an Associate, Quality Assurance Compliance focused on implementing and maintaining quality control practices to ensure product compliance with regulatory standards in medical devices and ophthalmic products. You will manage quality systems, change control, supplier quality management, conduct audits, and support adherence to cGMP and ISO requirements across functions.This remote role requires a Bachelor's degree or equivalent with 4–8 years of relevant#J-18808-Ljbffr
- What You’ll DoAs the QA Compliance Specialist, you’ll help ensure Anika’s manufacturing operations meet applicable quality, regulatory, and documentation requirements. Working in a regulated medical device and life sciences manufacturing environment, you’ll review production...Medical deviceFull timeInternshipWork at officeImmediate start
- ...Sentara Health is seeking a Remote Quality Improvement Specialist to review behavioral health claims for medical necessity and regulatory compliance. This is a fully remote role with opportunities across multiple states, including Oklahoma. You will evaluate clinical...Remote work
- ...Sharecare is seeking a Quality Control Specialist to review electronic medical records and perform HIPAA-compliant quality... ...supervisors, and upholding ROI laws. This remote, full-time position emphasizes accuracy and compliance in a fast-paced environment. #J-18808-LjbffrRemote workFull time
- ...seeking a Senior Staff Representative - Quality Assurance for a 100% remote role with 50% travel. The candidate will perform audits and investigations under CFR Title 14, Part 121.373, ensuring compliance across engineering, maintenance, and related programs.Minimum...Remote work
- ...OmniOn Power Inc. is seeking a Quality Assurance Specialist to audit engineering specifications and packages for accuracy, completeness,... ...The position reports to the Services Quality Leader and is 100% remote, with eligibility to work in the United States. Strong Excel/SharePoint...Remote work
- ...Piper Companies is seeking a GCP Quality Assurance Specialist to support a leading clinical research organization. This remote role requires residing in the DMV area (... ...periodic travel.You will maintain the QMS, administer QA training, conduct and support GCP audits, and...Remote work
- ...global healthcare leader, seeks a QA Specialist to support commercial QA and regulatory compliance across the EMEA region from... ..., ISO standards, and medical device regulations while coordinating... ...industries, plus experience with #J-18808-Ljbffr Remote Source, Inc.Remote workMedical device
$85k - $100k
...growing, Boston-based medical technology company using... ...Clinical Quality Assurance Specialist, you'll play a key role... ...Development, Software QA, Clinical, and... ...quality assurance or medical device software testing, including... ...if they prefer. Fully remote employees outside the...Remote workMedical deviceWork experience placementWork at officeFlexible hours$64.07k - $99.79k
...The Senior Compliance Reporting Specialist will be responsible for ensuring compliance with the Physician... ...Finance and Legal. **This is a REMOTE opportunity with preference to candidates... ...experience in a healthcare or medical device company 0-20% Travel This role is not...Remote workMedical deviceFull timeWork experience placementImmediate start- ...General Information Name: QA Specialist III Ref #: 16920 Posting date... ...6 Work Schedule: Full time Remote Work: In office Job: Q -... ...Responsibilities Monitor and enforce compliance with internal procedures,... ..., pharmaceutical, biotech, medical devices, food manufacturing)...Remote workMedical devicePermanent employmentFull timeTemporary workWork at officeShift work
$33 - $35 per hour
...Quality Assurance Compliance Specialist Kelly® Science & Clinical is seeking a Quality Assurance Compliance Specialist for our client, a leader in the medical device industry, in Clearwater, Florida. If you’re passionate about bringing the latest scientific discoveries...Medical devicePermanent employmentFull timeTemporary workWork at officeMonday to Friday$25 - $29.75 per hour
...Thursday, Friday can work remote/from home Top 3 things... ...'s Degree Required in Medical/ biological science/... .... 2. Quality/Compliance experience and working... ...Management systems in medical device industry or similar... ...role as a Compliance Specialist on the Enterprise Product...Remote workMedical deviceContract workWork experience placementWork from homeMonday to Friday- ...Job Description Quality Assurance Compliance Specialist Allendale, NJ Lynkx Staffing LLC specializes... ...the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. This... ...of study. ~5 years’ + experience in QA in a life sciences company with a strong...Medical deviceNight shift
$139.18k - $191.38k
...unique contributions. Varian Medical Systems, a Siemens... ...is seeking an onsite Product Compliance Specialist at our Headquarters in Palo... .... This role will allow some remote/hybrid flexibility but the successful... ...NRTL approvals for medical devices. ~ Knowledge of...Remote workMedical deviceTemporary workWork at officeLocal area- ...International Trade Compliance Specialist Dedicated Computing's international trade compliance... ..., international travel reviews, remote support, cloud access, and secure transfer... ...equipment, aerospace and defense, medical devices, telecommunications, industrial automation...Remote workMedical deviceTemporary workFor contractors
$38 - $56 per hour
...Solutions is seeking a Regulatory Affairs Specialist for a minimum 6-month remote contract opportunity. This... ...who have prior experience in the medical device industry. The ideal candidate will... ...regulatory requirements, medical device compliance, and regulatory documentation....Remote workMedical deviceHourly payContract workLocal areaImmediate startMonday to Friday- ...Cardinal Health is seeking a Proofreader – Global Labeling in Salem, OR to ensure 100% accuracy and regulatory compliance of global labeling graphics for medical devices. You will compare typescript to proofs, verify artwork, and provide feedback to designers to align with...Medical device
- ...is seeking Regulatory Affairs support to ensure ongoing compliance with U.S. FDA medical device requirements, ISO 13485, and related regulations. You will... ...across multiple regions while working with product, QA, and operations teams. The role includes coordinating Pre...Remote workMedical device
- ...45Reference26-01317Remote50% Remote Job Description: Highly experienced... ...Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the... ...knowledge of U.S. and international medical device regulations, strong...Remote workMedical device
- ...Title: Quality Assurance Specialist – Product Operations... ..., Inc. is seeking a QA Specialist to support... ...ensuring the quality, compliance, and reliability of our remote cardiac monitoring devices and related workflows.... ...cadence of a distributed medical device company. Key...Remote workMedical device
- ...Company is seeking a detail‑oriented Credentialing Specialist to review licenses, certifications, and background checks. This fully remote role supports onboarding teams across the United States and emphasizes accuracy, compliance, and timely processing. You’ll handle...Remote work
- ...OmniOn Power Inc. is seeking a Quality Assurance Specialist to audit engineering specifications and packages, ensuring accuracy and adherence... ...engineering, program management, and operations. Based remotely in the United States, you will support TL 9000 metrics,...Remote work
- ...seeking a Senior Regulatory Affairs Specialist to lead regulatory strategies for US... ...ensuring timely approvals for spinal devices and ongoing compliance across sections of regulatory... ...guiding junior staff in a fast-paced medical device environment. #J-18808-LjbffrRemote workMedical device
- Job-ID32466100Reference26-01017Remote50% Remote Job Description: Prepare regulatory... ...market distribution of new and modified medical devices (510(k)/NTF) in US, Canada, and EU. Support... ...risk-benefit analysis for regulatory compliance Submit and review change controls to...Remote workMedical deviceLocal area
- ...standards management, and submission preparation activities in a remote work environment. Key Responsibilities Support ongoing... ...Approximately 2-5 years of experience in regulatory affairs, quality, medical device, pharmaceutical, or related industries Working knowledge of...Remote workMedical device
- ...SpecialistLocation: New Haven, CT 3days onsite 2 remote Interview: 1 round of interviewPosition... ...responsible for ensuring quality and compliance of active GxP documentation and... ...related role in a GxP-regulated biopharma, medical device, or similar industry.Bachelor's degree...Remote workMedical deviceWork at office
$95k - $124k
...GDP audits, supporting supplier qualification, compliance oversight, and inspection readiness activities... ...providers, logistics partners, and/or medical device manufacturers.Plan, execute, and document on-site, remote, and hybrid interna/external audits.Assess compliance...Remote workMedical deviceFull timeContract workTemporary work- ...the full-time Senior Regulatory Specialist will prepare regulatory documents... ...labeling activities, and ensure compliance with global regulations in a remote setting. Key responsibilities... ...a regulatory specialist in the medical device or pharmaceutical industry Knowledge...Remote workMedical deviceFull time
- ...functional teams, the full-time Principal Regulatory Affairs Specialist will provide regulatory guidance, author submissions for medical devices, and monitor regulatory landscape changes while working remotely. Key responsibilities Serve as the regulatory...Remote workMedical deviceFull time
$95k - $115k
...Sr International Regulatory Affairs Specialist to join its growing Regulatory... ...European Union In Vitro Diagnostic Medical Devices Regulation (IVDR) and Medical Devices... ...international market access and ongoing compliance. This is a remote position that will report to the...Remote workMedical deviceFull timeWork at officeNight shift
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