Fda Regulations Jobs in Clifton, NJ
Fda Regulations Jobs in Clifton, NJ

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Job Description: The Patient Services Representative II (PSR II) represents the face of our company to patients who come in both as part of their health routine or for insights into life-defining health decisions. The PSR II draws quality blood samples from patients and prepares those 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...
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...
This well-established multi-specialty medical organization in Northern New Jersey is seeking a motivated and patient-focused Audiologistto join their growing team. With a rich history and a reputation for excellence in eye ear nose and throat care this organization has evolved into a 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...
WHAT DOES AN ART SUPERVISOR DO The Art Supervisor (AS) is an active contributor to the creative team taking full responsibility of concept and art/design development across various projects ranging in complexity and scope. The AS is a direct liaison between creative and junior/mi More...
WHAT DOES A GROUP COPY SUPERVISOR MARKET ACCESS DOThe Group Copy Supervisor (GCS) is an active contributor to the creative and strategic teams taking full responsibility of the work and owning concept and copy development on various projects across the portfolio ranging in complexity More...
WHAT DOES A COPY SUPERVISOR DO The Copy Supervisor (CS) is an active contributor to the creative team taking full responsibility of concept and copy development across various projects ranging in complexity and scope. The CS is a direct liaison between creative and junior/midleve More...
The Senior Manager Regulatory Affairs US Advertising and Promotion ImmunologyDermatology combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet the required legislation. Additionally the individual deve More...
Job Title: Specialist Quality EngineeringJob Code: 24025Job Location: Clifton NJJob Description: L3Harris is looking for a Quality Engineer to join its operations organization in Clifton New Jersey. Works independently. Proven ability to drive FRB/MRB activities to closure. Ability to 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...
Your CareerYoull help to ensure all of our outbound communications are current correct consistent customerfriendly and polished to perfection or close understanding when time simply wont allow for that last revision youd make if you could. You respect the boundaries between content More...
The Associate Director Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading crossfunctional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace More...
Your CareerYoull help to ensure all of our outbound communications are current correct consistent customerfriendly and polished to perfection or close understanding when time simply wont allow for that last revision youd make if you could. You respect the boundaries between content More...
Job Title: Associate Manager Quality ManagementJob Code: 23507Job Location: Clifton NJ Job Description: The Electronic Warfare Quality Control Associate Manager is responsible for the Operations Quality Inspection Team in support of Quality Inspection performance and execution across More...
The Associate Director Immunology Field Training Dermatology is responsible for the team developing the sales franchise curriculum for AbbVie field personnel and field management. This person will create lead and work within crossfunctional teams made of participants from Training Me More...
The Senior Manager Regulatory Affairs US Advertising and Promotion ImmunologyDermatology combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet the required legislation. Additionally the individual deve More...
Responsibilities: Candidate must be able to answer questions in the STAR format (Situation Task Action Result). If they cannot formulate a response this way please coach or whittle down the resume. Note answers should pull from multiple projects and not the same one over and over. C More...
About Our CompanyWere a physicianled patientcentric network committed to simplifying health care and bringing a more connected kind of care.Our primary multispecialty and urgent care providers serve millions of patients in traditional practices patients homes and virtually through Vil More...
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