📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...
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📑 Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection ...
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📑 Regulatory Affairs SpecialistThe Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. They will also coordinate clinical study trials, including offsite location fo ...
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📑 Job Title: Regulatory Affairs SpecialistLocation: 63103, St Louis, Missouri, United StatesDuration: 24 MonthsJob Description:With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks rela ...
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📑 ResponsibilitiesHeadquartered in Kobe, Japan, Sysmex is located in Lincolnshire, Illinois. Renowned worldwide for the very finest in quality, innovative diagnostic equipment and information-management systems, we apply science to enhance the quality of life on a global scale. Our agile, resourceful team is committed to re ...
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📑 Hybrid Senior Manager, Regulatory Affairs - Lincolnshire, IllinoisIntroduction:This is the time to let your talent come to life. Maximize your knowledge and use it for the greater good. Work with top professionals using state-of-the-art technology to improve lives with your innovative ideas and amb ...
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📑 Position SummaryBostonGene is seeking a Regulatory Manager to join our team and play a crucial role in supporting our ISO certification efforts and regulatory compliance. The primary focus of this position will be on ensuring Good Laboratory Practice (GLP) and ISO conversion for a team dedicated to assisting cancer patien ...
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📑 Are you a proactive, strategic thinker with hands-on expertise, driven to act, adaptable to changing directions and methods, and thrive in a dynamic, fast-paced environment?Do you excel at efficiently managing multiple priorities, effectively communicating with all organizational levels, and bring an immediate and valuable cont ...
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📑 Responsibilities: Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy for US and International submissions.Timely compilation of materials for license renewals, updates, and registrations<br ...
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📑 Walker Cole International is searching for a QA/RA Specialist to join a Global Medical Device business in Massachusetts, Boston. As part of this role you will manage a the regulatory compliance of a range of medical devices including IVD's (In Vitro Diagnostics) focussing on ensuring compliance through QMS management and complaint management.</p ...
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📑 Regulatory Affairs Specialist II – On-site in Scarborough, ME RESPONSIBILITIESImplement & maintain the effectiveness of the quality systemSupport manufacturing/operations day to day activities for change controlAssist regulatory specialist in change control- and product devel ...
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📑 Currently seeking a Regulatory Affairs Associate for a prominent client of ours. This position is located in St. Louis, MO. Details for the position are as follows:Job Description:Shift: Monday-Friday 1st shift (This is a hybrid role manager is looking for someone to go onsite 2-3 days a week)<br / ...
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📑 Regulatory Affairs Associate – Abbott Park, IL Must be able to work on a W2Job Summary: As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes ...
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📑 Opportunity to join a global diagnostics company at their HQ just outside of Chicago, focused on the strategy for existing and new product submissions to the FDA and Canada. Leading a small team, this is for somebody with prior Regulatory management experience and knowledge of IVD requirements.Main Responsibilities</ ...
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📑 The position of Regulatory Affairs Specialist II is within our client's Infectious Disease business unit. In this role, you will prepare documentation for EU Technical Files and international product registrations. TERM & START 1-year contract starting 6/10/24 with possibility to ex ...
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📑 Title: Regulatory Affairs SpecialistLocation: Scarborough, MEShift: Mon - Fri | 8am to 5pmRESPONSIBILITIES: Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR). Provides regulatory s ...
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📑 Job Title: Regulatory Affairs ExpertJob Location: St. Louis, MO (Hybrid 2-3 days onsite)Job Duration: 24 Months- TEMP TO PERM POTENTIAL Your Role:With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory task ...
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📑 Responsibilities: Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products' registration. Participate on product development teams, providing regulatory strategies, timel ...
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📑 Responsibilities: Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products' registration. Participate on product development teams, providing regulatory strategies, timelines, an ...
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📑 Regulatory Affairs Expert Contract Duration 12 Months Your Role:With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new ...
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📑 2 openings2 year contract w/ temp to perm potentialYour Role:With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes ...
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📑 Responsibilities:As a Senior Research Scientist specializing in In Vitro Diagnostics (IVD) materials, you will play a pivotal role in advancing our research and development efforts. Your responsibilities will include:Research and Development:Lead and contribute to the design and development of innov ...
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📑 Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing ...
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📑 6-9 month contract Part time (up to 20 hrs per week)Hybrid work schedule in Fremont, CAClient in medical devices industryJob Description: The Technical Writer/Graphic Illustrator will be responsible for the planning, preparation, and maintenance of formal documentation, illustrations ...
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📑 A fast-growing orthopedic Medical Device company in Irvine, CA is in immediate need of a Regulatory Affairs Consultant to support them for approximately 3 months. The consultant will need to work onsite at least 3 days/week.The Regulatory Affairs Consultant will be focused on the hands-on developm ...
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📑 DivIHN (pronounced “divine”) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have b ...
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📑 At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.As a Zimmer Biomet team member, you will share in our commitment to providing mobility and ...
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📑 UNICEF works in some of the world’s toughest places, to reach the world’s most disadvantaged children. To save their lives. To defend their rights. To help them fulfill their potential. Across 190 countries and territories, we work for every child, everywhere, every day, to build a better world for everyone. And we never give ...
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📑 DivIHN (pronounced “divine”) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have b ...
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📑 Responsibilities: Provides strategic global regulatory guidance to cross-functional project teams responsible for product development. Actively leads the development and implementation of regulatory strategies for assigned programs and ensures cross-functional alignment. <br ...
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📑 Title: Regulatory Specialist - OnsiteDescription: ...
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📑 DivIHN (pronounced “divine”) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have b ...
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📑 We are seeking an experienced Quality Manager to join our team in the IVD (In Vitro Diagnostic) industry. The ideal candidate will have a minimum of 10 years of relevant experience in the medical device manufacturing sector, with a strong background in quality management systems, regulatory compliance, and ISO standards. The Quality Manager will pl ...
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📑 We are seeking an experienced Quality Manager to join our team in the IVD (In Vitro Diagnostic) industry. The ideal candidate will have a minimum of 10 years of relevant experience in the medical device manufacturing sector, with a strong background in quality management systems, regulatory compliance, and ISO standards. The Quality Manager will pl ...
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📑 The Sales Director will play a critical role in shaping and executing CorDx's sales strategy in the rapidly evolving IVD market. This position is responsible for driving sales growth, building and maintaining strong customer relationships, and leading the sales team toward achieving and surpassing sales targets.Key Responsibilities: ...
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📑 The Sales Director will play a critical role in shaping and executing CorDx's sales strategy in the rapidly evolving IVD market. This position is responsible for driving sales growth, building and maintaining strong customer relationships, and leading the sales team toward achieving and surpassing sales targets. Key Responsibili ...
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📑 Job Description:As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remain ...
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📑 Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countrie ...
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📑 Company Overview:Avails Medical, Inc. is a well-funded medical device start-up, based in Menlo Park, California. At Avails we are developing a novel electrical point-of-care bio-sensor platform for rapid infectious disease detection.Position Overview: ...
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📑 Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countrie ...
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📑 Regulatory Specialist IIScarborough, ME6+ month’s contractResponsibilities: Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR).Provides regulatory suppor ...
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📑 IMMEDIATE CONTRACT NEED! (16 MONTH CONTRACT). OPEN TO REMOTE IN U.S. (EST HIGHLY PREFERRED).Looking for someone with hands on experience supporting and implementing Veeva Vault RIM Registrations platform is required. Veeva certification desiredIn this role, you will partner with Regulatory Affairs business a ...
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📑 Designs and performs sophisticated, technically challenging experiments, efficiently and independentlyGenerates effective hypotheses to pursue Project goals and set new experimental directionsMakes substantive conceptual contributions to Project activities and scientific strategiesDevelops novel and creative solut ...
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📑 Kelly® Science & Clinical is seeking a Sub-Investigator for a fulltime, direct-hire position with a research site in Tampa, FL. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. The Sr. Clinical Researc ...
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📑 The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing and metrology, to a broad range of scientific R&D and QC measurements. Proven quality and trustworthy perform ...
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📑 Regulatory AffairsRegulatory Affairs SMECompensation: $110,000 to $130,000Location: Shelbyville, INABOUT OUR CLIENT:Our client is a leader in their space, in SE Indianapolis. Their state-of-the-art facility will< ...
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📑 CorDx, a leader in the biotechnology industry, is seeking an experienced and strategic Marketing Director to join our growing team. As a Marketing Director at CorDx, you will be responsible for developing and implementing innovative marketing strategies to drive brand awareness, increase market share, and generate revenue. You will lead a team of m ...
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📑 CorDx, a leader in the biotechnology industry, is seeking an experienced and strategic Marketing Director to join our growing team. As a Marketing Director at CorDx, you will be responsible for developing and implementing innovative marketing strategies to drive brand awareness, increase market share, and generate revenue. You will lead a team of m ...
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📑 Position : Government Affairs and Advocacy and Information Technology (GAA/IT Intern) Reports to: Vice President, Government Affairs and Advocacy (GAA) Department: President's Office Location: Washington DC (Remote) Length: 10 weeks, June 10 to August 16 Sche ...
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📑 DivIHN (pronounced “divine”) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have b ...
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