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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 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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📑 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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📑 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 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Senior Director, Regulatory Affairs - Permanent - HybridProclinical Staffing is seeking a Senior Director, Regulatory Affairs to join a cutting-edge AI company. This is a permanent role with the opportunity to work hybrid in California.Skills & Requirements:Accomplished Regulatory professional with extensive experience forged within the Medical Dev ...

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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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Exciting opportunity with a leading global pharmaceutical company dedicated to improving the health and well-being of patients worldwide. With a focus on innovation, quality, and accessibility, they are committed to developing and delivering high-quality pharmaceutical products that make a positive impact on people's lives.Position Overview: This c ...

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📑 Senior Vice President of Medical, Regulatory, and Pharmacovigilance reports directly to the CEO and holds a strategic leadership role.and manages Pharmacovigilance, Regulatory Affairs, and Medical Affairs departments, ensuring their success in achieving departmental and company-wide goals.motivates, and develops high-performing teams, fostering a c ...

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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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📑 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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📑 The Senior Director of Regulatory Affairs will be responsible for the full range of regulatory matters related to our products and compliance with industry regulations, both internal and external,including:general regulatory monitoring and compliance, regulatory analysis of new productdevelopment opportunities, issue-specific advocacy on our own be ...

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📑 We are partnered exclusively with an exciting biotech company who are looking to bring on their first hire within their regulatory affairs department. Role can be at Director or Senior Director level.The team are looking for individuals with the following experience:Authoring and submitting an IND (the company is a year away from submitting its fir ...

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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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📑 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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📑 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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📑 Senior Director, Regulatory Affairs*Bay Area- Hybrid*Meet has partnered with a fantastic Bay Area pharma focused in treatments for metabolic, psychiatric, and oncologic disorders. Our client has an approved product and a dynamic late-stage pipeline. You will be coming in to lead their Oncology portfolio and you'll be reporting into the VP of Regula ...

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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 Market Access Product Strategy Manager The Senior Market Access Product Strategy Manager will report to the Senior Director Market Access and will help to shape bioMérieux’ s market access strategy primarily for existing on-market products and collaborate with global teams to provide insights to shape the pre- ...

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📑 Would you like to apply your global Regulatory Affairs strategy expertise and passion to make an impact in a company that follows the science and turns ideas into life changing medicines?At AstraZeneca, we do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing! We continuously forge ...

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📑 Embark on an Extraordinary Career Journey with Us!At The Center for Health Affairs and CHAMPS Healthcare, we're more than just a workplace; we're a passionate community driven by exceptional talent. We prioritize your success. Whether you're looking to advance in your current role or explore ...

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📑 Title: Senior Medical Director, Clinical DevelopmentDescription: The Senior Medical Director, Clinical Development is a vital contributor to clinical development programs, overseeing study-specific activities, collaborating with cross-functional teams, and supporting regulatory activities. Responsibilities include protocol design, data analysis, co ...

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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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📑 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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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researchin ...

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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researchin ...

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📑 Senior Legislative Manager or Legislative Manager (One Position)About MCEMCE is a not-for-profit public agency that has set the standard for clean energy in our communities since 2010. We provide renewable power at stable rates and deliver cutting-edge energy programs to residents and businesses across four Bay Area counties: Contra Costa, Marin, N ...

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📑 Why Endo?We want the best and brightest people at Endo to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward ...

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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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📑 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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📑 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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📑 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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📑 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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📑 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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