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Regulatory Affairs Consultants Jobs

Company

Pharmatech Associates, a USP company

Address San Francisco, CA, United States
Employment type FULL_TIME
Salary
Category Pharmaceutical Manufacturing
Expires 2023-08-03
Posted at 10 months ago
Job Description
We are looking for a Regulatory Affairs Consultant to support several ongoing projects at about 10-20 hours per week. This role is remote.


Job Duties


  • Experience working with government agencies sponsoring drugs and biologics is highly desirable. Combination Drug and Device regulatory submission experience is a plus.
  • Work closely with Pharmatech and our client’s executive leadership team to lead the development of regulatory strategies and objectives that result in the successful registration and post-approval commercialization of the client’s product.
  • Provide regulatory guidance to the Client across all areas of regulatory affairs throughout all stages from product development
  • Participate as part of internal regulatory team to define and execute the regulatory strategy
  • Plan and oversee activities in support of all regulatory submissions
  • Serve as the primary company contact with the US FDA to achieve company regulatory objectives, by fostering strong relationships and acting as a credible, reputable, and effective advocate for company
  • Support the preparation of briefing packages, and regulatory submission documents as needed , providing insight and expertise
  • Develop, lead, and drive the execution of the regulatory strategy from pre-IND to launch, commercialization and product lifecycle management


Education And Qualifications


  • Proven record in submission of licenses and authorizations for the maintenance of existing products; International registrations and dossiers and execution of regulatory strategies that align with business deliverables
  • Plans schedules for regulatory deliverables on a project and monitors project through completion
  • Responsible for communicating business-related issues or opportunities to next management level
  • Provide Regulatory Affairs support during internal and external audits
  • Advanced degree from accredited college or university in science, biomedical engineering, plus a minimum of 10 years of experience in Filing Global Regulatory Applications for the following registrations NDA’s, ANDA’s, IND’s and BLA’s for pharmaceutical and Biotech products.


Pharmatech Associates, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.