Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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Janssen Research & Development, LLC Director, Regulatory Affairs in Raritan, New Jersey

Employer: Janssen Research & Development, LLCJob Title: Director, Regulatory AffairsJob Code: A011.5200Job Location: Raritan, NJJob Type: Full-Time Rate of Pay: $230,000 - $263,000Job Duties: Responsible for the development, implementation, and maintenance of robust Global / North American regulatory strategies. Lead the Global Regulatory Team and be a key contributor on multiple cross-functional teams, such as Compound Development Team (CDT). Provide strategic direction to the teams. Provide critical reviews of key Health Authority submissions such as IND/CTAs, meeting requests, briefing documents, response documents and marketing, and supplemental applications. Ensure that regulatory strategies are in alignment with product portfolio, regional strategies, CMC Regulatory Affairs strategy, commercial and market access strategy, and the Target Product Profile (for global programs as assigned). Lead and/or participate in meetings with FDA, Health Canada, EMA, and other Health Authorities (HAs) as appropriate. Develop a regulatory strategy that will deliver global and/or regional needs with initial focus on the key markets identified. Ensure business compliance, support due diligence activities, implement drug development strategies, and adhere to regulatory standards. Establish North American content requirements and timing for global dossier plans including BLA/NDAs, IND/CTAs, as well as addendums & supplements. Serve as primary point of contact for US FDA. Lead the regulatory response team for FDA and Health Canada questions. Ensure US Business Partners are consulted and given input into US regulatory strategies, PMR fulfillments, and other US-related issues. Manage routine maintenance submissions. Manage and track NA post-approval commitments. Provide input and review submission documents, as well as approve submissions before dispatching to regulatory authorities. Contribute to the development of the USPI. Lead the development of NA labelling negotiation strategies and development of supporting documentation for labelling. Review FDA and Health Canada labelling to ensure consistency with the CCDS and ensure that annotations are complete and correct.May telecommute from anywhere in the U.S.Requirements: Employer will accept a Bachelor’s degree in Regulatory Affairs, Pharmaceutical Sciences, or related field and 10 years of progressive, post-baccalaureate experience in the job offered or in a Director, Regulatory Affairs-related occupation.CONTACT: To apply, please send resume to jkim6240@its.jnj.com. Please refer to Job #A011.5200

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