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📑 Regulatory Affairs Project Manager – Structural Heart page is loaded Regulatory Affairs Project Manager – Structural Heart Apply locations United States - Minnesota - St. Paul time type Full time posted on Posted 2 Days Ago job requisition id 31082167 Abbott is a global healthcare leader that helps people live mo ...

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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 countries.* ...

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📑 Regulatory Affairs Project Manager – Structural Heart page is loaded Regulatory Affairs Project Manager – Structural Heart Apply locations United States - Minnesota - St. Paul time type Full time posted on Posted 3 Days Ago job requisition id 31082167 Abbott is a global healthcare leader that helps people live mo ...

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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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📑 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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📑 Title: Clinical Project Manager - OncologyLocation: Texas-based Candidates Position Overview: As a Clinical Project Manager specializing in Oncology, you will play a pivotal role in overseeing the planning, implementation, and execution of clinical trials for our oncology drug development programs. You will collaborate closely with cross-functional ...

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📑 As a Medical Affairs Manager, you will play a pivotal role in bridging the gap between the medical and commercial aspects of our organization. This position involves collaborating with various stakeholders, including internal teams, healthcare professionals, and regulatory bodies, to ensure the successful integration of medical strategies into over ...

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📑 Bachelor's Degree in Engineering or related field requiredMaster's Degree may offset some experience requirementsPeople management experience required - including providing coaching and feedback, responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relationsDesign Quality or Enginee ...

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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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📑 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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📑 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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📑 Job Title : Manager/Associate Director, Health Economics and Outcomes Research (HEOR)Location: 100% Remote Duration: 12 Months Candidate Requirements: s MS or PhD in Health economics, Pharmacoeconomics, health services research, public health or related field. s Experience with development and execution of economic modeling strategies s Experience ...

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📑 Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is ...

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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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📑 Work at ROCKET PHARMA and help cure rare diseases!Rocket Pharma is a fully integrated, clinical-stage company advancing gene therapies with curative potential for multiple rare childhood diseases. Rocket places enormous value on people and considers team member progress and well-being to be as important as the progress of its pipeline. We are looki ...

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📑 McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care. What you do at McKesson matters. We foste ...

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📑 If you are passionate about innovation and have the ambition to be a key-player in the transformation of medicine, join us! You will be welcomed in the WeHealth Digital Factory team, and be part of the project management group, a dynamic and growing team to pilot e-health solutions dedicated to our patients and healthcare pro ...

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📑 The Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at Workday@Genmab.com . Associate Director/Senior Manager, Global Regulatory Affairs Project Lead page is loaded Associate Director/Senior Manager, Global Regulatory Affairs Project ...

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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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📑 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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📑 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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📑 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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📑 The Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at Workday@Genmab.com . Associate Director, Global Regulatory Affairs CMC page is loaded Associate Director, Global Regulatory Affairs CMC Apply locations Copenhagen ti ...

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📑 This structural engineer role is fully hands-on, providing the opportunity to work with various clients daily. If you're a design expert and want to grow with a growing firm, this is the opportunity for you!What You Will Be DoingHandle structural design projects from inception to completion, including planning, scheduling, and coordinating tasks to ...

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📑 Reference Number: JO-2402-530393Senior Regulatory Affairs Scientific LeaderRate: NegotiableJob Type: PermanentLocation: United States Exciting opportunity at a fast-growing biotech The team are looking for a regulatory affairs scientific lead that has excellent knowledge and skills in CMC, GMP and regulatory affairs.Resp ...

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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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📑 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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📑 Salary: $200,000-$230,000Associate Director Clinical OperationsSan Francisco, CA (Hybrid)Job DescriptionEmbark on a transformative career with our innovative biotech venture nestled in the heart of San Francisco, where innovation meets impact in the realm of oncology. We are on a relentless pursuit of redefining cancer treatment through the precisi ...

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📑 **Regulatory Affairs Department Manager, Kfar Saba - OSD, Sterile and Biologics****Location:** Kfar Saba, IL, 1111 ****Company Info****Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core o ...

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📑 Mantell Associates is partnered with a growing Clinical Research site in their search for a Manager to join their Clinical Operations team. Clinical Operations Manager - Responsibilities:Manage vendor relationships and deliver on clinical portfolioMaintain and report on program budgets, such as long-range forecasting and monthly accrualsMaintain ap ...

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📑 Head of Medical Writing - Permanent - OnsiteProclinical is seeking a Head of Medical Writing to join a cutting-edge biopharmaceutical company. This is a permanent role located in San Francisco, CA.Primary ResponsibilitiesThe Head of Medical Writing will be responsible for providing leadership and strategic direction to the medical writing function, ...

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📑 Engineer (I, II, or III) – Structures Inspection ProgramFull-time employment opportunity with a dynamic and multi-faceted resource for economic development in the St. Louis region.About UsSince 1950, we have partnered with private and public organizations on hundreds of projects that have created thousands of jobs on both sides of the Mississippi R ...

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📑 Welcome. You haven’t signed in yet so please select ‘I accept’ to start or access your Jacobs Career Application. My Account Options Your Impact: At Jacobs, we’re not just building structures, we’re helping our clients innovate and grow by designing, engineering, and executing the construction of their state-of-the-art facilities that are ...

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📑 This clinical-stage biotech company is revolutionizing the treatment of cancer. They are seeking a Vice President of Regulatory Affairs to oversee all regulatory activities including serving as the primary contact with FDA and other regulatory agencies. You will develop and implement regulatory strategies, lead Health Authority interactions, and ov ...

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📑 This clinical-stage biotech company is revolutionizing the treatment of cancer. They are seeking a Vice President of Regulatory Affairs to oversee all regulatory activities including serving as the primary contact with FDA and other regulatory agencies. You will develop and implement regulatory strategies, lead Health Authority interactions, and ov ...

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📑 Structural (Bridge) EIT-(SOU0003RN) Your Impact: If you are ready to bridge the gap between our world and our people, join Jacobs. Let’s build for a brighter future together. Jacobs is much more than just a traditional engineering company. As a vital member of our Florida & Puerto Rico team, you’ll have ...

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📑 Associate Director, Regulatory Affairs, Advertising & Promotion—New JerseyTanner and Associates is recruiting an Associate Director, Regulatory Affairs, Advertising & Promotion for a Pharmaceutical Company. This Job is located in New Jersey. Responsibilities: Provides strategic and operational leadership in advertising and promotion for the US mark ...

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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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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to ...

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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to ...

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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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📑 Director, US Regulatory Affairs Strategy page is loaded Director, US Regulatory Affairs Strategy Apply remote type Hybrid Work Arrangement locations Basking Ridge, NJ time type Full time posted on Posted 2 Days Ago job requisition id R2533 Join a Legacy of Innovation 110 Years and Countin ...

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📑 Vice President, Government & Regulatory Affairs About the Company Global leader in sustainable energy solutions & services with diverse gas-supply sources IndustryOil & Energy TypePublic Company Founded2008 Employees10,001+ Categories EnergyOil and GasNatural ResourcesElectricalB2BOil & GasE-com ...

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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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📑 Director of Policy & Regulatory Affairs | Eastern US, REMOTE |$165k - $175k base + bonusAre you a regulatory affairs and energy policy professional with experience in the RTOs (PJM), FERC and State Commissions?Are you looking for an opportunity to join a small, well-backed, company on the cutting edge of the clean energy transition?Do you enjoy kee ...

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📑 1123 open jobs. Use your resume to get matched with the right job. Upload your resume Vice President – Public Policy and Government Affairs Washington, DC, United States and 1 more LA-Legal Director, Managing Counsel-Regulatory Policy / Market Structure – Public Policy and Government Affairs Washington, DC, United States and 1 more LA-Legal ...

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📑 Associate Director, Global Regulatory Affairs - Early-Development ** Rare Diseases ** PIP's and ODD's** Boston, MAWe have a new RA Associate Director position with a Greater Boston-based Rare Disease Biotech, which is well-funded with a broad portfolio of TA's and indications across a variety of modalities who are led by a talented and highly regar ...

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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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