Regulatory Affairs Job at Merck, Rahway, NJ

  • Merck
  • Rahway, NJ

Job Description

Manufacturing & Quality Assurance ( 47 ) jobs Marketing ( 23 ) jobs Medical Affairs ( 6 ) jobs Other ( 4 ) jobs Policy & Communications ( 3 ) jobs Regulatory Affairs ( 11 ) jobs Research & Development ( 63 ) jobs Supply Chain ( 7 ) jobs About Us We are one company, but we operate under two different corporate brand names. We are known as Merck & Co.,Inc., Rahway, New Jersey, USA in the United States, Canada & Puerto Rico. We are known as MSD everywhere else. Learn more about our hybrid work model. Discover how we support our employee’s physical, mental, financial and social well-being to help them fulfill their potential Be Yourself Our culture values a diversity of voices and always bringing your best self to work. Job Search, Application & Interview Tips Frequently Asked Questions The Physician Payment Sunshine Act (PPSA) Join our Talent Community to stay connected and receive updates on the latest job opportunities. This site is for Residents of the United States, Canada & Puerto Rico. Residents of other markets, please click here . Our Regulatory Affairs teams advance communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare discoveries that help provide new and compliant medical products, practices, and solutions to the world. Location Rahway, New Jersey, United States of America Job Type Full time Signal management statement preparation and, if applicable, submission to Competent Authorities according to timelines outlined in applicable regulations.... The CSRM Physician works closely with cross-functional team members including those from clinical development, epidemiology, regulatory affairs, statistics, and manufacturing to manage safety topics under... Under the general direction of the Clinical Safety and Risk Management (CSRM) Therapeutic Area (TA) Lead and Vice President, Chief Safety Officer, the Executive Director for CSRM will be responsible for... Under the general direction of an Executive Director, General Medicine, the CSRM Principal Scientist is a leader in drug safety and is responsible for overall clinical risk management and safety surveillance... Serve as an Alternate Liaison with the USDA for pre and/or post-regulatory responsibilities to include submissions and communications with the USDA, internal company departments and international permittees... Location West Point, Pennsylvania, United States of America Job Type Full time This position reports to the Director, Clinical Supplies Quality and will have responsibility for operational management, capacity planning and scheduling for clinical finished goods and supporting activities... The Associate Director of Regulatory Affairs is responsible to independently support new product development and certain geo-expansion activities by developing pre- and post-approval Chemistry, Manufacturing,... Ensuring automation systems are maintained in a validated state, as part of an active/ongoing lifecycle management program and in compliance with Current GXP requirements. Providing support for small startup... Demonstrated ability to generate innovative solutions to complex regulatory problems and effectively work with and communicate to key stakeholders. The incumbent is expected to be knowledgeable in project... Independently interacts with worldwide regulatory agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or more our company's investigational and marketed... This careers website is intended for Residents of the United States, Canada & Puerto Rico. Residents in other markets, please visit our MSD Careers page. Information on this site is for the purpose of presenting career opportunities at our organization and give our audience a view of our culture, diversity and growth opportunities. Our Company is an equal opportunity employer, Minority/Female/Disability/Veteran, proudly embracing diversity in all of its manifestations. #J-18808-Ljbffr

Job Tags

Full time, Worldwide,

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