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📑 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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📑 Consultant, Regulatory Specialist, Tissue Bank/PharmaceuticalSummaryOur client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. This position will report to a Manager within the Regulatory department. This individual will play a crucial role in ensuring compliance with regulatory requiremen ...

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📑 Consultant, Regulatory Specialist, Tissue Bank/PharmaceuticalSummaryOur client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. This position will report to a Manager within the Regulatory department. This individual will play a crucial role in ensuring compliance with regulatory requiremen ...

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📑 Oldcastle Infrastructure™, a CRH company, is the leading provider of utility infrastructure solutions for the water, energy, and communications markets throughout North America. We’re more than just a manufacturer of precast concrete, polymer concrete, or plastic products. We’re a trusted and strategic partner to engineers, contractors, distributor ...

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📑 Director of Product Compliance Caesars is one of the biggest names in the world of betting and we are striving to become the largest sports betting and iGaming platform in America. We share in our passion to be industry leaders, providing best-in-class service for all our customers. Our Product Technology team has built a prop ...

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📑 Why Choose Jefferson Health Plans?We are an award-winning, not-for-profit health maintenance organization offering Medicaid, Medicare, and Children’s Health Insurance Program (CHIP) plans that include special benefits to improve the health and wellness of our members. We are committed to creating a community where everyone belongs, acknowledges, an ...

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📑 Regulatory Affairs Expert-Medical Devices1 Year (Temp to perm) St Louis, MO (Hybrid 2-3 days onsite)Pay: $33.00/hr 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 products, and chan ...

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📑 Regulatory Affairs Expert-Medical Devices1 Year (Extendable & potential to convert) St Louis, MOMax PR: $25-33/hr 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 products, and chang ...

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📑 Position SummaryThe primary responsibility of the Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The RAS is also responsible for ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory activities required for our client's ...

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📑 Company DescriptionPower Dream is a dedicated participant in the global Energy Curing industry, specializing in oligomers, monomers, and additives. With over 20 years of experience, we prioritize innovation, eco-friendliness, substance, and responsibility. Our goal is to introduce cutting-edge technologies to diverse markets including graphic arts, ...

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📑 Robert Half Legal is partnering with a manufacturing organization with a World Wide presence is currently looking to hire a Director of Regulatory Compliance. This position is fully in-office and can sit at one of their three corporate headquarters being Greater Hartford CT, Greater Buffalo NY, or Greater Dallas TX.Ideal Candidates will have:7+ yea ...

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📑 Title: Regulatory Affairs Associate Location: New Jersey (ONSITE) Job Type: 12-Month Contract Start Date: ASAP Reputable pharmaceutical client is seeking a Regulatory Affairs Associate to join their Regulatory Affairs team on a long-term contract. The ideal candidate will have 1-3 years of experience, hands-on experience with publishing submissions ...

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📑 A fintech firm located in Orange County, CA who’s looking to bring on board a “Regulatory Compliance Officer” to their team. They are currently growing at a rapid pace and looking for superstars. You do not need fintech experience for this role although it is a plus. They are in office (5 days/week). Responsibilities:• Monitor and test compliance w ...

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📑 RESPONSIBILITIES: Responsible for technical writing of files in accordance with In Vitro Diagnostic medicaldevice Regulation (IVDR). Provides regulatory support for diagnostic product development and commercialdiagnostic products. Develops regulatory strategies for products in development and for modified products toachieve clearance/approval in ...

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📑 This opportunity is with a company revolutionizing the medical device industry with its cutting-edge technologies and commitment to addressing unmet healthcare needs. At the heart of their success is the culture of innovation. The company fosters a dynamic environment where creativity and collaboration thrive. With a diverse team of engineers, rese ...

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📑 Position Title: Regulatory Affairs InternLocation: Washington, DC (Hybrid)Reports to: Vice President, Senior Counsel, Regulatory AffairsAccepting applications for Fall 2024 (Sept.17 - Nov. 26) Company Background:MFA, based in Washington, DC, New York, Brussels, and London, represents the global alternative asset management industry. MFA’s mission i ...

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📑 My client in the Triad area has a Direct hire Opportunity for a Regulatory Compliance Engineering Supervisor!The Regulatory Compliance Engineering Supervisor is responsible for managing the daily operations of the Flammability and Durability testing labs, while developing testing protocols that ensure products meet or exceed industry standards. Thi ...

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📑 Join Jubilant Radiopharma as our Director of Regulatory Affairs and be at the forefront of revolutionizing healthcare through innovative radiopharmaceuticals.About Us: Jubilant Radiopharma is a dynamic leader in the development and distribution of cutting-edge radiopharmaceuticals, dedicated to advancing medical imaging and therapeutic solutions wo ...

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📑 Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office and partly remote. Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Will work on IND submissions (publishing and structure of the IND, not ...

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📑 Are you passionate about product analysis and regulatory compliance? Are you looking for a remote opportunity that allows you to utilize your strong analytical and problem-solving skills? If so, we have an exciting opportunity for you as a Remote Product Analyst!In this role, you will be an active participating member of our dynamic produ ...

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📑 Job DescriptionThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering c ...

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📑 The Quality Engineer designs quality standards, defines monitors, and improves processes needed to meet customer and regulatory requirements. This role is responsible for identification of problems and implementation of preventative and corrective actions for suppliers, customers, and internal processes. The Quality Engineer leads and mentors o ...

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📑 RBW is partnering with an innovative, rare disease biotech in their urgent and business-critical search for a new Associate Director, Regulatory Affairs. This position will be in charge of developing and implementing short, mid and long-term global regulatory strategies that support the success of both clinical and commercial products globally.They ...

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📑 Our customer is looking for a Senior Regulatory Affairs Specialist to join a team of 7 and supporting the product submissions, regulatory guidance, and registering products. Duties Include:Maintain and establish regulatory functions for medical device and environmental compliance.Uphold Quality Management System for domestic and international stand ...

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📑 Title: Director/Senior Director of Regulatory Salary: $200,000 to $270,000Summary: An Oncology based biotech client of ours is looking to fill their Director/Senior Director role based out of their facility in the San Francisco Bay Area. They are looking for very committed and passionate candidates who can collaborate with their colleagues to help ...

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📑 Petroplan is seeking an HSE Enviornmental & Regulatory Supervisor to join an industry-leading independent oil and natural gas exploration and production company local to Texas. Job SummaryThe Environmental and Regulatory Supervisor oversees compliance efforts for our clients operations in the US Onshore-Eagle Ford Shale (EFS) region, ensuring adher ...

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📑 Must be able to be on site 3 days per week in the San Francisco Bay Area! Key ResponsibilitiesProvide strategic and operational regulatory guidance for cross-functional teams, including CMC, non-clinical, and clinical, in collaboration with project teams and regulatory colleagues.Contribute to the development of global clinical regulatory plans, pr ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 Major, Lindsey & Africa’s Interim Legal Talent group has an immediate need for temporary to permanent Healthcare Transactional and Regulatory Attorney.Overview: Our Law Firm Client is interested in growing its Healthcare Team.Company: Regional Powerhouse Law Firm with 115+ Attorneys.Experience: 8+ years Healthcare Transactional and Regulatory.Locat ...

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📑 The Sr. Manager, Regulatory will report to the VP, QC/Regulatory and help provide leadership and management direction for all regulatory compliance activities on a domestic and international level across all brands. They will provide knowledge of current and future regulations regarding cosmetic ingredients, raw materials, packaging, labeling, clai ...

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📑 Senior Director, Regulatory Affairs (Generalist)Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and w ...

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📑 Vice President Regulatory Affairs (Medical Device) - ONSITE in Bay AreaOur esteemed client, a inovative and growing medical device company specializing in the manufacturing of implantable medical devices. They are looking for a Vice President Regulatory Affairs to spearhead regulatory strategies that will shape the future of healthcare and continue ...

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📑 Meets clinical-stage biopharmaceutical client based in the Bay Area is seeking a highly motivated individual to join their growing regulatory affairs group. The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's r ...

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📑 As part of the continued growth and innovation of our Capital Project Delivery service offering, ERM has an opportunity for an experienced biologist/regulatory specialist to join our thriving global consulting firm as a Principal Biologist/Regulatory Specialist in Northern California (Walnut Creek or Sacramento offices).The ideal candidate will hav ...

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📑 RBW is partnering with an innovative late clinical-stage, oncology Biotech (140 FTE) in their urgent and business-critical search for a new Director/AD, Regulatory Affairs. Our client is focused on discovering and developing precision medicines for the treatment of rare cancer and solid tumours.The candidate will report directly to the Head of RA, ...

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📑 Our client, an exciting and growing Biotech Company, is seeking a Regulatory Affairs professional at the Senior Director level. This role will lead the North America regulatory strategy and work extremely closely with the C-Suite leaders of the business. They are focused on Autoimmune diseases and are based in New Jersey. This is a hybrid role with ...

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📑 A Pharmaceutical business in New Jersey is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will serve as the regulatory lead on relative Review Committees, for products in the Rare Disease, Rare Blood Disorders and the companies Neurology portfolio.Responsibilities:Represents Global Regulatory Affai ...

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📑 Global Regulatory Affairs Specialist – Remote MUST BE ABLE TO WORK ON A W2Job Title: Global Regulatory Affairs Specialist Job Summary: The Regulatory Affairs Specialist will be the regulatory representative for assigned due diligences, under the direction of the Global Regulatory Strategy Lead (GRSL). An external company and assets or individual as ...

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📑 Senior Regulatory Affairs Specialist (Medical Devices) - Hybrid (Bay Area)Our client is a growing Imaging Medical Device company that is making a meaningful impact on patient lives. They are looking for a Senior Regulatory Affairs Specialist with a track record of bringing imaging devices to market.Responsibilities:Prepare and submit regulatory sub ...

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📑 Summary: Our client, a leading pharmaceutical company based in Delaware is seeking an experienced and assertive decision maker to join their team. They are seeking an Associate Director for Global Regulatory Labeling Strategy to be responsible for all activities related to labeling documents throughout the product life cycle. Experience in Regulato ...

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📑 Our client, a Reputable, Global Pharmaceutical Company, is seeking a Regulatory Affairs Strategy professional at the Director level. This role will advise, develop and implement regulatory strategies for specific assets within Oncology. The position will report directly into the VP of Regulatory Affairs. The company is growing exponentially with a ...

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📑 A long-term international consulting client of X4 Life Sciences is looking to add a Director, Regulatory Affairs to their rapidly growing team.Our client focus on providing their clients with solutions to their most difficult drug development challenges whilst providing unique expertise to prepare datasets, reports, global regulatory submission doc ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 Senior Manager Regulatory Affairs - (Medical Device) - Hybrid in MNOur client is an, looking for a Senior Manager Regulatory Affairs with extensive experience with 510(k) submissions. As the Senior Manager Regulatory Affairs you will be the liaison for communication with US and international regulatory agencies for multiple submissions across the c ...

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📑 The role involves providing global regulatory oversight and project leadership for assigned development products, reporting directly to the Vice President of Regulatory Affairs. The incumbent will contribute to and execute regulatory strategies to facilitate global product development, oversee regulatory communications with health authorities, and ...

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📑 A leading biotechnology firm specializing in dermatology research and development is looking for an Associate Director, Regulatory Affairs. Position Summary: The Associate Director of Regulatory Affairs will play a pivotal role in driving regulatory strategy and execution for our dermatology-focused biotech initiatives. Reporting to the Director of ...

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📑 Associate Director/Director, Regulatory Affairs (Oncology)Remote - East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director or Director of Regulatory Strategy to join their team. This role will be reporting into the VP ...

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📑 THE COMPANY : Juul Labs’ mission is to impact the lives of the world’s one billion adult smokers by eliminating combustible cigarettes. We have the opportunity to address one of the world’s most intractable challenges through a commitment to exceptional quality, research, design, and innovation. Backed by leading techno ...

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📑 Solutions Architect Role Overview: As a Solutions Architect, you will be responsible for designing and implementing comprehensive technical solutions that address complex business challenges. Leveraging your expertise in Azure and other IT tools, you will collaborate closely with internal stakeholders to gather and tra ...

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📑 Job Description Basic troubleshooting, installation, maintenance and repair on designated equipment. Supporting customer applications and equipment process optimization. Completing Preventive Maintenance and field modifications and upgrades. Ordering and coordinating replacement parts.</l ...

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