Description:
- Assist in preparing responses to global information requests and related maintenance documentation (amendments, supplements, annual reports, safety reports, etc.) within a defined schedule.
- Help determine regulatory strategies for manufacturing changes and regulatory activities.
- Aid in preparing Lifecycle Management like Annual Reports (Product, DMF).
- Coordinate and track workflows for regulatory submissions.
- Ensure regulatory submissions meet global standards.
- Participate in meetings and interact with project team members and sub-teams.
- Assist with and eventually lead licensing activities and required updates (Establishment Registration, California State License, State licensing).
- Support reporting requirements under the CARES Act.
- Provide support to Regulatory management as needed.
SKILLS:
- PC literacy is required.
- Proficiency in technology use, including MS Office skills (Outlook, Word, Excel, PowerPoint, MS Project), Document Management Systems and Internet resources, is expected.
- General knowledge and application of global regulations and cGMP requirements are necessary.
- Must be able to work independently and with appropriate supervision.
- Excellent organizational, interpersonal, and communication skills (oral and written) are required.
EDUCATION:
- A Bachelors degree in a scientific field, preferably Chemistry or Pharmacy, with 1-3 years of experience, or a Masters Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required.
About US Tech Solutions:US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To learn more about US Tech Solutions, please visit . US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.