📑 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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📑 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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📑 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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📑 Clinical Trials Regulatory Research Associate - RemotePay: $34.78 - $55.92/hourHours: 8:00am - 4:30pm PST*This is a 6-month contract positionDepartment Overview:The Clinical Trials Office administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical ...
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📑 Job Title: Regulatory Affairs OfficerCompany: Biopharma OrganizationLocation: Hybrid, RTP AreaBrio Resource Group is a Life Sciences Executive Search Firm committed to providing rare talent on an exclusive search basis to the Biopharma, Pharma, Device and CRO industries. We work on behalf of organizations that value true talent acquisition partners ...
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📑 Regulatory Affairs ConsultantCambridge MA, Remote with occasional site timeMedical Device6 month contract - 40 hours per weekCompetitve hourly rateA MedTech company based in Massachusetts specializing in Class 2 Medical Device solutions are looking to hire a contractor for a 6-month renewable contract to support with product submissions in multiple ...
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📑 PURPOSE STATEMENT: This position will be responsible for managing and coordinating implementation of regulatory requirements across all Blueroot Health brands, reflective of both the FDA CFR section 111 and the Company’s policies and practices. This coordination includes making sure the Company is fully compliant and meeting all requirements for ...
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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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📑 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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📑 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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📑 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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📑 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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📑 Role Title: Regulatory Compliance SpecialistDuration: 6 monthsWork Location: San Francisco, CA (Can work remotely)Work Schedule: M-F 9a-5p (strongly preferred to be US Pacific Time)NOTE: I am not able to work on a C2C basis or provide sponsorship/visa transfers at this time.Project Overview: Our client’s Regulatory Compliance team is searching for ...
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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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📑 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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📑 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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📑 My client is a market leading biopharma, developing and manufacturing innovative biologic immunotherapies using best-in-class patented processes, driving a new way forward for patients suffering with infectious diseases. The Regulatory Affairs Manager will lead the preparation of regulatory submissions to the FDA, providing guidance on responses to ...
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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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📑 My client are looking for a Regulatory Affairs Specialist with experience in Asia Pacific Product Registrations.You MUST be willing to work hybrid in office at Exton, Pennsylvania.Essential Duties and Responsibilities:Author and review China, South Korea, Japan and additional submissions as well as US and EU SubmissionsWork cross functionally with ...
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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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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There are currently 1,328,769 total jobs available in United States according to American Jobs.