Exponent

FDA CVM Regulatory Managing Scientist (D.V.M, Ph.D., or M.S.)

Exponent$127K — $156K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • DVM (preferred), Ph.D., or Master’s degree in a science-related field
  • Five or more years of FDA CVM or FFDCA regulatory experience
  • Consulting experience preferred
  • Excellent oral and written communication skills
  • Detail-oriented with strong time management skills
  • Ability to manage multiple projects with competing deadlines
  • Excellent interpersonal skills and collaboration experience

Responsibilities

  • Provide regulatory and technical strategy for FDA CVM approval of animal drugs
  • Compile and submit various regulatory filings related to animal drugs
  • Utilize expertise in FDA CVM technical areas like CMC and labeling
  • Evaluate regulatory information for FDA CVM submissions
  • Draft and proofread complex regulatory reports
  • Engage with clients and regulators during the application process
  • Manage client project deliverables, invoices, and budgets

Benefits

  • Support for health and well-being programs
  • Competitive benefits including compensation and recognition programs
  • Flexible work schedule allowing for work/life balance
  • Collaborative and inclusive work environment
  • Opportunities for career growth and future success planning
Full Job Description
Our Opportunity

We are currently seeking an FDA CVM Regulatory Scientist for a Managing Scientist level position for our Chemical Regulation and Food Safety Practice to be based in our Washington, DC office. Other locations may be considered. In this role you will work as part of a team providing a high level of FDA CVM guidance, project management, technical expertise, and project support to the consultants in the Chemical Regulation and Food Safety Practice in relation to US Food and Drug Administration Center for Veterinary Medicine drug filings.

You will be responsible for
  • Provide high-level regulatory and technical strategy related to Food and Drug Administration (FDA) Center for Veterinary Medicine (CVM) approval for new and generic animal drugs
  • Author, compile, and submit regulatory filings for New Animal Drug Applications, Investigational New Animal Drug files, Abbreviated New Animal Drug Applications, Supplemental New Animal Drug Applications, and Conditional New Animal Drug Applications
  • Expertise in some or all relevant FDA CVM technical areas, including CMC, effectiveness, target animal safety, human user safety, and labeling
  • Evaluate and synthesize technical and regulatory information in support of FDA CVM submissions, including but not limited to new registrations, supplemental applications to registered animal drugs, and ongoing stewardship requirements
  • Draft, edit, and proofread complex regulatory and technical reports
  • Engage directly with clients and regulators throughout the strategy development, application submission, and review process for new and generic drugs
  • Manage and track client projects, project deliverables, invoices, and budgets
  • Participate in developing business and marketing to clients
You will have the following skills and qualifications
  • DVM (preferred), Ph.D., or Master’s degree in a science-related field
  • Five (5) or more years of FDA CVM or the Federal Food, Drug, and Cosmetic Act (FFDCA) regulatory experience. This position requires knowledge, solid understanding, and practical experience with U.S. FDA CVM/FFDCA regulations for animal drugs.
  • Consulting experience preferred (but not required)
  • Excellent oral and written communication skills, including the ability to independently prepare, edit, and proofread technical and regulatory documents
  • Must be detail-oriented, able to work independently, and manage time effectively
  • Strong ability to organize and prioritize multiple projects with competing deadlines
  • Excellent interpersonal skills and ability to work in a collaborative environment
  • Experience with project management, budget tracking, and invoicing a plus
  • Exposure to sensitive information will necessitate considerable use of tact, diplomacy, discretion, and judgment
  • Entrepreneurial spirit is a plus
  • Presently legally authorized to work in the United States.  No immigration sponsorship or processing required. 

 

Applicants are encouraged to submit a CV with publications (feel free to include publications that are in review or pending) [not restricted to 1 page].

Life @ Exponent

To learn more about life at Exponent and our impact, please visit the following links:https://www.exponent.com/careers/life-exponenthttps://www.exponent.com/company/our-impact

 

Attracting, inspiring, developing, and rewarding exceptional people with diverse backgrounds and expertise are central to our corporate culture. Our diverse team allows us to provide better value to our clients and enjoy an enriched work environment.

Our firm is committed to offering a variety of programs and resources to support health and well-being. We believe that providing competitive benefits as well as compensation and recognition programs empowers our staff to do work that makes a difference.

Work Environment

At Exponent, we have found that in-person interactions deepen employee engagement and are crucial for development, for realizing the full potential of our talented and diverse teams, and for​ building a more inclusive workplace where all have a sense of belonging. In our offices, you can expect a supportive culture and a collaborative, dynamic, multi-disciplinary work environment. Our consultants engage in-person in the office unless they are traveling for client work or other business activities.

 

We value the rich lives our colleagues enjoy outside of work and understand that work/life balance is critical to our employees and their well-being. Consultants have the autonomy to balance their work and personal schedules so you can meet with clients, visit inspection sites, attend conferences, and make time for priorities outside of work, too. It is this flexible, agile work style and working hours that allow our teams to drive innovation and results in their own ways, while meeting the needs of clients. #LI-Onsite

Compensation

Our consultants are rewarded for their technical and business contributions and have an opportunity to plan for future success and career growth. Exponent's total compensation plan is consistent with its expectations of the quality and quantity of work performed and with the professional standards set by Exponent. At the Manager level and above total compensation includes base salary, annual bonus, and 401(k) employer contribution of 7% of base salary.

The base salary range for this position is dependent on experience and capabilities which will be assessed during the interview process.

Salary RangeUSD $127,000.00 - USD $156,000.00 /Yr. Benefits you will enjoy

Access benefits information on our Life@Exponent page:https://www.exponent.com/careers/life-exponent

 

Job LocationsUS-Washington, DC

About Exponent

Exponent is a multi-disciplinary engineering and scientific consulting firm that brings together more than 90 different disciplines to solve engineering, science, regulatory, and business issues facing our clients. The company has been providing solutions to complex problems for more than 50 years and has a reputation for technical expertise, objective analysis, and clear communication. Exponent's services include analysis and testing, engineering and design, human factors, environmental and health sciences, and regulatory consulting. The company serves clients in a wide range of industries, including aerospace, automotive, consumer products, energy, healthcare, and technology.
Learn more about Exponent
Size
1,215 employees
Market Cap
$5 billion
Industry
Net Income
$82.5 million
Founded
1967
5 Year Trend
+8.2%
Revenue
$399.9 million
NASDAQ

Similar Jobs

More Jobs at Exponent

More Pharmaceuticals & Biotech Jobs

Find similar FDA CVM Regulatory Managing Scientist (D.V.M, Ph.D., or M.S.) jobs: