Fda Regulations Jobs in Princeton, NJ
Fda Regulations Jobs in Princeton, NJ

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Project Manager, Global Regulatory Affairs Compliance And Planning
Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based company ou More...
Associate Director â Us Breyanzi Commercialization Analytics
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the la More...
Associate Director, Analytical Ai Forecasting And Predictive Solutions
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the la More...
Associate Director, Immunology Commercialization Analytics
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the la More...
Job Description: The Patient Services Representative I (PSR I) represents the face of the company to patients who come in both as part of their health routine or for insights into life-defining health decisions. The PSR I draws quality blood samples from patients and prepares those sp More...
At Genmab we are dedicated to building extranotordinary futures together by developing antibody products and groundbreaking knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain More...
Associate Director, Compliance & Ethics Investigations
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the la More...
At Genmab we are dedicated to building extranotordinary futures together by developing antibody products and groundbreaking knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain More...
Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based company ou More...
Job Description: Responsible for planning writing implementing and reviewing computer system validation (CSV) protocols of GxP computerized systems. Serve as the CSV subject matter expert and provide guidance on and interpretation of global GxP guidance and regulations of computerized More...
Privias Platform Operations team is a team composed of subject matter experts on our proprietary products technology onboarding and integrations clinical data conversion and interfaces. They manage the projects intake feedback support prioritization processes metrics and communication More...
The Creative Director (CD) Copy Market Access is a manager and leader of brands who sets the bar in terms of craft for senior-level copy team members. The CD has a proven ability to multitask delegate and manage as appropriate to ensure seamless management of business while still cont More...
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the la More...
Associate Director, Analytical Ai Innovation And Excellence
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the la More...
At Genmab we are dedicated to building extranotordinary futures together by developing antibody products and groundbreaking knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain More...
The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...
Associate Director Payer Enrollment is responsible for facilitating the enrollment program and serves as the primary enrollment liaison for clinics payers billing office and practitioner related issues.Primary Job Duties:Ensure protocols are being followed to ensure timely resolu More...
Associate Director, Field Analytics And Commercial Insights
The RoleModerna is seeking an Associate Director Field Analytics & Commercial Insights to lead the execution of data-driven analytics and performance reporting in support of our U.S. field team. This role plays a critical part in shaping how customer engagement insights inform fie More...
Director, Global Drug Safety & Pharmacovigilance Scientist
At Genmab we are dedicated to building extranotordinary futures together by developing antibody products and groundbreaking knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain More...
Roles & Responsibilities: Develop and execute validation protocols for computer systems. Ensure compliance with regulatory requirements and industry standards. Create detailed validation documentation including plans reports and scripts. Conduct risk assessments and impact analyses r More...
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