Vice President Regulatory Affairs Quality Assurance

Job DescriptionJob DescriptionOur Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with counterparts, investigators, project team members, and consultants. Lead/support...

Job DescriptionJob DescriptionOur Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with counterparts, investigators, project team members, and consultants. Lead/support...

Job DescriptionJob DescriptionOur Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with counterparts, investigators, project team members, and consultants. Lead/support...

Job DescriptionJob DescriptionOur Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with counterparts, investigators, project team members, and consultants. Lead/support...

Job DescriptionJob DescriptionPMV Pharmaceuticals Inc.Job Description: Executive Director, Head of Regulatory AffairsReports to: Chief Development OfficerLocation: Hybrid (2 days a week in Princeton, NJ office)Position OverviewThe Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the...

Job DescriptionJob DescriptionPMV Pharmaceuticals Inc.Job Description: Executive Director, Head of Regulatory AffairsReports to: Chief Development OfficerLocation: Hybrid (2 days a week in Princeton, NJ office)Position OverviewThe Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the...

PMV Pharmaceuticals Inc. Job Description: Executive Director, Head of Regulatory Affairs Reports to: Chief Development Officer Location: Hybrid (2 days a week in Princeton, NJ office)Position Overview The Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the company meets its objectives....

Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes. Integra LifeSciences, a...

Office Administration Provide reception responsibilities for the office while creating a welcoming atmosphere and providing helpful information and guidance to phone, mail, email, and in person inquiries. Exercise sophisticated phone etiquette, excep Vice President, Office, Associate, Assistant, President, Project, Education, Business Services

Job DescriptionJob DescriptionVice President, Sales – Sintetica USSintetica US, Princeton, New Jersey, On site or Remote201-500 employees · Pharmaceutical ManufacturingAbout the jobFounded in 1921 and headquartered in Mendrisio (Switzerland), Sintetica's mission is to continuously strive to improve therapies by enhancing its products' formulations...

Coordination of and Support for Institutional Committees and Groups - 40%Under the direction of the Vice Provost for Academic Affairs, organizes staffing, supports, and contributes to the development of critical academic goals across institutional co Associate, Program, Support, Project Management, Skills, Education, Business Services

summary Position Description: The QS Associate will supervise the activities with development, application, training, and maintenance of quality standards for industrial processes at Vytalogy Wellness. The QS Associate will also be assisting with ensuring that all products meet the established quality standard according to "The Code of Federal regulations...

Job Description: We are currently looking for a highly motivated hands-on Lead Quality Assurance Analyst with demonstrated experience in leading and proactively participating in the end to end system testing process within a fast paced trading environment. This person should be well-versed in leading automated testing efforts within the context of a...

Our client is looking to fill the role of Medical Affairs Consultant. This position will be fully remote.Responsibilities:Collaborating with Medical Affairs colleagues and external vendors to execute asset strategy and tactical plans with appropriate use of resources and according to developed timelinesTracking priority Medical Affairs tactics and...

**About the Department*** The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new...

10+ Years of experience is mandatory. The Business Analyst will engage and partner with cross-functional business teams to gather business requirements perform gap analysis develop functional requirements define solution recommendations draft business cases perform vendor research partner with internal and external development and testing teams to...

10+ Years of experience is mandatory. The Business Analyst will engage and partner with cross-functional business teams to gather business requirements perform gap analysis develop functional requirements define solution recommendations draft business cases perform vendor research partner with internal and external development and testing teams to execute...

Job DescriptionJob DescriptionMMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable...

Job Title: Senior Regulatory Operations Specialist About this role: The Senior Regulatory Operations Specialist position is an integral part of MRM for Health and the Regulatory Operations capability. Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and...

Role & Responsibilities Strong working in the Medical Affairs. Work with Med. Affairs team to create initial SOP creation and revision Websites Digital document storage and retention and Inspection Readiness preparation. Create review track and manage clear and concise medical information including Standard Response letters and fulfillment of ad hoc...