Senior Medical Writer - Medical Devices & Regulatory
PPG US ProPharma Group, LLC
ProPharma Group in the United States seeks an experienced Medical Writer to lead cross-functional projects, author regulatory and clinical documents, and mentor junior writers. The role emphasizes strong communication with clients and internal teams to ensure on-time, compliant deliverables. The candidate should have 7+ years of experience in writing clinical/regulatory documents for drugs, biologics, or devices, and a solid grasp of FDA and ICH guidelines, with hybrid work options and a #J-18808-Ljbffr PPG US ProPharma Group, LLC
- ...supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global... ...Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret...SeniorRegulatoryMedical deviceRemote jobFull timeWorldwide
- ...expertise that empowers biotech, med device, and pharmaceutical... ...With deep domain expertise in regulatory sciences, clinical research solutions... ..., pharmacovigilance, medical information, and R&D technology... ...less experienced medical writers, as necessary. ~ Adheres...RegulatoryMedical deviceContract workWork at officeRemote work
- ...Senior Manager Quality Engineering - Neurosurgery - 3686014 Join an innovative medical device company seeking a Senior Quality Manager to take ownership of the Quality function... ...FDA inspection readiness and support regulatory audits and inspections. Partner cross...SeniorRegulatoryMedical deviceFull timeContract work
- MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and...SeniorRegulatoryRemote job
- Senior Medical Writer - Clinical Development Immix Biopharma, Inc. United States / Remote / LA, CA Our 3 Core Values Intelligence Integrity... ...department, responsible for preparing, reviewing, and editing regulatory documents required for submission to the U.S. Food and Drug...SeniorRegulatoryOdd jobRemote work
- ...22Remote50% RemoteJob Description: The Senior Computer System Validation (CSV) Engineer... ...as pharmaceutical, biotechnology, or medical device manufacturing. This role ensures that systems... ...in compliance with FDA, EU, and global regulatory requirements. The Senior CSV Engineer...SeniorRegulatoryMedical device
- ...is an engine of innovation, helping pharmaceutical, biotech, medical device, and diagnostic companies develop custom solutions that tackle... ...planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. #J-18808-Ljbffr GuidehouseSeniorRegulatoryMedical deviceImmediate start
$120k - $165k
...patients, at the right time.Senior Manager, Companion Diagnostics... ...diagnostic validation, ensuring regulatory compliance and timely study... ...for running clinical device studies, including adherence... ...demonstrated experience in IVD or medical device development with a minimum...SeniorRegulatoryMedical deviceFull time- ...practice supports pharmaceutical, biotech, medical device, and diagnostic companies in product planning, pricing, reimbursement, and regulatory solutions. This role leads project teams... ...mentor consultants, collaborate with senior leaders, and participate in sales and practice...SeniorRegulatoryMedical device
- ...digital platforms in biopharma. This role focuses on regulated non-medical-device software used in healthcare and digital health, guiding... ...product lifecycle. You will collaborate with Product, Engineering, Regulatory, Cybersecurity, and Data teams to develop quality procedures,...SeniorRegulatoryMedical device
- ...data-focused clinical research organization, invites a senior Medical Writer to guide regulatory documentation and regulatory submissions. You will mentor... ...driving innovative solutions for pharmaceutical, biotech, and medical device clients worldwide. #J-18808-Ljbffr MMSSeniorRegulatoryMedical deviceWorldwide
- ...CAPA and nonconformance resolution, and own field quality and complaint investigations. The role reports to the SVP of Quality and Regulatory and collaborates closely with Manufacturing, Supply Chain, and Engineering to ensure inspection readiness and continuous #J-1880...SeniorRegulatoryMedical deviceContract work
- ...or Aliso Viejo, California office. As a Senior Quality Engineer, you will:Lead... ...maintenance of host systems supporting Tempus Medical Device(s).Lead risk assessments to determine testing... ...and FDA guidance, other applicable regulatory requirements, as well as best practices...SeniorRegulatoryMedical deviceFull timeWork at officeRemote work3 days per week
- ...edge technology to improve lives? As a Senior Design Quality Engineer at Gilero, A Sanner... ...the quality development of new medical device and combination products; from ideation... ...Translate user needs, intended use, regulatory inputs, and risk controls into measurable...SeniorRegulatoryMedical deviceWork experience placementWork at office3 days per week
- ...and capabilities to provide regulatory compliance, disputes, and investigations... ..., nursing, pharmacy, medical science, economics,... ...healthcare technology, medical devices and/or diagnostics), with experience... ...at a Partner/Director/Senior Management level --- OR a combination...SeniorRegulatoryMedical deviceFull timeRemote work
- ...and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only...SeniorRegulatoryMedical deviceRemote job
$80k - $200k
...experienced consultant to lead MedTech Regulatory Information Management (RIM) implementations... ...Affairs specifically within the Medical Device or Diagnostics industryDirect experience... ...exerciseA final conversation with our group's Senior Leader.Once all interviews are complete...SeniorRegulatoryMedical deviceWork at officeLocal areaRemote workWork from home3 days per week- ...support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global... ...career. Visit or follow MMS on LinkedIn. Senior Pharmacovigilance Physician distinction...SeniorRegulatoryMedical deviceRemote job
- ...and industry-leading employee retention. We support the pharmaceutical, biotech, and medical device industries with our proven scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains...SeniorRegulatoryMedical deviceRemote job
- ...Senior Technology Auditor GE HealthCare (GEHC) is a leading global medical technology and digital solutions innovator. Our purpose... ...such as Manufacturing, Medical Devices, Technology, Consulting or... ...General knowledge of legal, regulatory and compliance requirements....SeniorRegulatoryMedical deviceWorldwideFlexible hours
$110.7k - $218.3k
Position Summary Senior Consultant - Product Quality & Safety... ...& Risk Our Deloitte Regulatory, Risk & Forensic team helps client... ...understand how Commercial and Medical activities and related messaging... ...pharmaceutical and medical device Regulatory Affairs and...SeniorRegulatoryMedical deviceLocal area$110.7k - $218.3k
Position Summary Senior Consultant - Digital Quality & ComplianceOur Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted... ...environment, including pharmaceutical, biotechnology, medical device, or clinical environmentsExperience leading...SeniorRegulatoryMedical deviceVisa sponsorship$86.7k - $173.3k
...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000... ...compliance with all corporate policies, procedures, and regulatory requirements. Required Qualifications ~ Bachelor's...SeniorRegulatoryMedical deviceWork at office$131k - $198k
...Salesforce Life Sciences Cloud, Senior ConsultantOur Deloitte Customer team empowers... ...the workforce.An evolving customer and regulatory landscape, mounting pipeline of next-gen... ...technology firms to global big pharma to medical devices, to drive business value through end-to...SeniorRegulatoryMedical deviceLocal areaVisa sponsorship$105k - $145k
...patients, at the right time. Senior Technical Product Manager for... ...diagnostic products, clinical regulatory requirements for software... ...significant experience in regulated device development. This role will... ...Significant experience in medical device development and regulatory...SeniorRegulatoryMedical deviceContract work- ...OPPORTUNITY: We are seeking a Senior Verification & Validation... ...wearable sensors and medical monitoring system solutions.... ...Product Management, Quality/Regulatory, and the Engineering teams (SW... ...industry required; ~ Medical device experience (Class II/IIb) strongly...SeniorRegulatoryMedical deviceFull timeContract workWork at officeWorldwideRelocation
- ...THE OPPORTUNITY: We are hiring a Senior Accountant to own the day-to-day accounting... ...supply chain, real inventory, and real regulatory obligations. You will drive the monthly... ...follow your name. Experience at a medical device, life sciences, or other regulated...SeniorRegulatoryMedical deviceFull timeContract workWork at officeWorldwide
$163.4k - $322.1k
...capability for Life Sciences clients. This Senior Manager role sits at the intersection... ...and procurement for biopharmaceutical, medical device, and broader life sciences... ...others The team In an evolving customer and regulatory landscape, a mounting pipeline of next-...SeniorRegulatoryMedical deviceStart working todayLocal areaFlexible hoursShift work$130k - $152.5k
...pharmaceutical, biotechnology, diagnostics and medical device companies achieve optimum performance... ...practice work on project teams with senior and junior consultants on a variety of... ...across the biopharmaceutical, regulatory and related life sciences industries.Senior...SeniorRegulatoryMedical deviceWork experience placementWork at officeWork from home3 days per week$118.3k - $207.4k
...Senior Legal Counsel page is loaded## Senior Legal Counselremote type: Hybrid (8 days... ...do business, build better judicial and regulatory systems. We help them get it right.**Who... ..., including but not limited to medical device regulations applicable to clinical/pharmacy...SeniorRegulatoryMedical deviceWork at officeRemote work
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