📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Lead SAP FICO Consultant Lead Consultant - US 117581BR Job Description Infosys is seeking a Lead SAP FICO Consultant This position is a key player in the consulting team that helps discover and define the problem statement, evaluates the solution options and makes recommendatio ...
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📑 Description Background Mercy Corps is a leading global organization powered by the belief that a better world is possible. In disaster, in hardship, in more than 40 countries around the world. Mercy Corps partners to put bold solutions into action — helping people triumph over adversity and build stronger communi ...
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📑 The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will b ...
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📑 Lead Mechanical Engineer - Lyophilizers Lead Mechanical Engineer opportunity to work for a top 10 premier CDMO. This position is working on a well funded site that will be growing over the next 3 years. You will be responsible for executing equipment improvement and capital projects in a cGMP setting associated wit ...
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📑 Lead Mechanical Engineer - Lyophilizers Lead Mechanical Engineer opportunity to work for a top 10 premier CDMO. This position is working on a well funded site that will be growing over the next 3 years. You will be responsible for executing equipment improvement and capital projects in a cGMP setting associated wit ...
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📑 Lead Mechanical Engineer - Top 10 CDMO Lead Mechanical Engineer opportunity to work for a top 10 premier CDMO. This position is working recently invested site that will be significantly growing over the next 3 years. You will be responsible for executing equipment improvement and capital projects in a cGMP setting ...
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📑 Lead Mechanical Engineer - Top 10 CDMO Lead Mechanical Engineer opportunity to work for a top 10 premier CDMO. This position is working on a recently invested site that will be significantly growing over the next 3 years. You will be responsible for executing equipment improvement and capital projects in a cGMP set ...
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📑 Exciting Opportunity in Regulatory Affairs - Sr. Director Location: Redwood City, CA (Onsite 3 days per week)Company Overview:A pioneering biotechnology company, at the forefront of cortisol modulation research and development, is seeking a dynamic Regulatory Affairs Sr. Director to join their innovative team. With a robust ...
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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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📑 Our client is looking to fill the role of HEOR Consultant. This position will be fully remote. This position serves as the lead for HTA launch readiness projects for Nephrology products. Supports under the Director, Health Outcomes this individual will develop elements of a dossier, Systematic lit reviews and HE models, used to deliver on eviden ...
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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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📑 Principal – Business Consulting (ServiceNow IRM Architect) Principal 118356BR Job Description Position: Principal- Regulatory Change Management, Risk and Compliance - ServiceNow IRM Architect Infosys Consulting – What We Do We are a leader in advisory ...
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📑 Position Summary As part of the Professional Services, Practice Delivery team, the Software Implementation Consultant, Financial will act as the principal liaison with the customer to implement best practices to drive optimized business outcomes for the customer within the Long-Term and Post-Acute Care (LTPAC) set ...
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📑 Senior Director, Regulatory Affairs (Generalist)Hybrid Role - 3 Days in Menlo Park, CAMeet 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 ...
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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, a ...
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📑 Oracle SCM O2C and P2P Functional Consultant/Business Architect. Lead Consultant - US 116737BR Job Description Infosys is seeking an Oracle SCM O2C and P2P Functional Consultant/Business Architect. The position will primarily be responsible for implementing, giving solutions in O2C, ...
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📑 Senior Director of Regulatory AffairsMenlo Park, CA Life Science People are currently working with an exciting client, looking for a Sr. Director Regulatory Affairs professional with a strong background in oncology submissions. My client is looking for someone to come in and le ...
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📑 Role: PLM QMS Consultant Location: Fort Worth, TX ( 100% Remote ) Duration: Full Time Must Have-PLM , QMS, implementation, Medical devices. Note: Experience running PLM Lifecycle must be strong and reflective in the resume. Job Description: - 15+ ...
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📑 Our client is seeking a Sr. Director, Clinical Regulatory Affairs to develop regulatory strategies for both non-clinical and clinical programs and lead interactions with regulatory authorities. Reporting to the SVP, Head of Regulatory Affairs, this role will have significant strategic oversight of various submissions and will be the global regul ...
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📑 The Brands and Innovative Medicines Global Regulatory Affairs organization is seeking a Senior Director, Global Regulatory Portfolio Leader. Working with leaders across the organization, this individual will provide leadership for the regulatory strategy of one or more in-line and pipeline assets in one or more therapeutic areas and develop a te ...
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📑 Principal - Communications Digital Transformation Consultant - ServiceNow Principal - Business Consulting 118228BR Job Description Infosys Consulting’s Communications Practice is seeking a Principal Level Management Consultant with experience implementing transformation solutions leveraging ...
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📑 Job Family:Management ConsultingTravel Required:Up to 50%Clearance Required:NoneWhat You Will Do:The Banking, Insurance and Capital Markets practice works with financial ind ...
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📑 Program Lead Assessor (ISA) - High-Speed Rail, USA EWI are supporting a leading consultancy firm, who are currently seeking Program Lead Assessor for an upcoming High-Speed Rail project in California, USA Responsibilities:Be accountable for the technical content of all Independent Safety Assessor (ISA) deliverables.Create and maintain the ISA Manag ...
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📑 Immediate opportunity for a Global Regulatory Affairs Manager II to work with a leading, global medical device company focused on vision research and eye health. This position will independently provide tactical and strategic leadership on complex EU MDR projects within the Global Regulatory Affairs organization by actively compiling and authori ...
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📑 At Seqirus, we are on the front line of fighting Influenza. Thinking big, working together and focusing on keeping people healthy are part of our core fundamentals. The Nordics Medical Affairs Lead is a regional health professional/scientist acting with integrity and striving to improve overall efforts to improve public health and ...
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📑 The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Lead for a prominent Pharmaceutical client of ours. This position is in Bridgewater, NJ (Hybrid Role). Details for the position are as follows: Job Description: Pay: (phone number removed)/hr on ...
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📑 Location: Boston, MA (Remote)Therapeutic Areas: NeuroJob Overview: The Associate Director/Director will develop and implement global regulatory strategies, serving as the regulatory lead for clinical studies and obtaining necessary approvals for initiation, amendme ...
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📑 Dynamic work environment and team focussed culture Career opportunities and support for professional development Picturesque NE Victoria location close to regional attractions Who are we? Albury Wodonga Health (AWH) is the largest regional health service between Sydney and Melbourne, located in the ...
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📑 Hybrid - 3 days a week in office - Princeton, NJ The Associate Director of Regulatory Affairs Labeling will assist in the development of a cross-functional labeling strategy for products worldwide, including providing expert input on labeling requirements and strategic guidance during label development, facilit ...
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📑 Position Title: Vice President of Medical AffairsIndustry: BiotechnologyEmployment Type: Full-timeLocation: Boston Massachusetts Equal Employment Opportunity: This company is an equal opportunity employer and is comm ...
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📑 CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives.With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspi ...
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📑 SUMMARY DESCRIPTION 1) Independently provide EU regulatory requirements and guidance to EU MDR project teams. 2) Lead the preparation of the EU MDR technical documentation for Class III, IIa, IIb, or Class I sterile or reusable medical devices to support timelines for CE marking and EU commercial release. 3) Lead the s ...
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📑 Position Overview:Astria Therapeutics is dedicated to bringing hope with life-changing therapies to patients and families affected by allergic and immunological diseases. Astria’s pipeline includes our lead program, STAR-0215, a monoclonal antibody inhibitor of plasma kallikrein in clinical development for the ...
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📑 Responsibilities:Lead the development and execution of regulatory strategies for PMA submissions, ensuring alignment with company goals and regulatory requirements.Oversee the preparation, review, and submission of PMA applications to regulatory authorities, including the FDA.Provide guidance and ex ...
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📑 C&M International (CMI) is a global government relations, public policy, and public affairs firm that helps clients promote their business priorities across three core pillars – Global Health, Digital Transformation, and Trade & Investment.Job DescriptionCMI is seeking accomplished candidates to provide st ...
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📑 US Regulatory Affairs Lead ------------------------------------------------------------------------------------------------- SCOPE OF RESPONSIBILITIES: He/She will be responsible for representing regulatory function to approve promotional material He/She will be at ...
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📑 Careers That Change Lives <div ...
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📑 Employment : Fulltime Office Location : Dallas, Texas Remote Work : Allowed Travel : 15% Job Description Oracle Cloud Projects (PPM) functional consultant is responsible for working closely with our Clients to help them implement Oracle Cloud solutions and be the SME in Pr ...
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📑 Title: Regulatory Affairs Manager Location: San Jose, CA Base Salary: $140,000-$190,000About:Currently working with a medical device company dedicated to developing and commercializing breakthrough catheter devices t ...
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📑 Principal - Communications, Media & Entertainment Principal - Business Consulting 117373BR Job Description Infosys Consulting’s Communications Practice is seeking a Principal Level Management Consultant with experience across one or more domain areas in the Communications industry, including ...
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📑 Job Posting: ATTORNEY III Inspector General's Office JC-409240 - ATTORNEY III ATTORNEY III $10,536.00 - $13,526.00 per Month Final Filing Date: 1/8/2024 Application Methods: Electronic (Using your CalCareer Account) By Mail Drop-off Job Description and Duties <b ...
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📑 Job Posting: ATTORNEY IV Inspector General's Office JC-409237 - ATTORNEY IV ATTORNEY IV $11,644.00 - $14,954.00 per Month Final Filing Date: 1/8/2024 Job Description and Duties CANDIDATES THAT PREVIOUSLY APPLIED FOR THE ATTORNEY IV POSITION WITH A FINAL FILING DAT ...
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📑 Role Title: Senior Manager/Associate Director, Regulatory Affairs CMCDepartment: Regulatory AffairsFLSA ExemptCORE VALUES Respect ● Passion ● Teamwork ● Integrity ● Honesty ● Commitment ● Collaboration<str ...
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