In this versatile and diversified role, you are responsible for managing our Regulatory Affairs for the US facility and fulfill US Agent responsibilities for all foreign Siegfried sites. Additionally, you will be managing all drug master files for the US facilities and maintain FDA Drug Registrations, FDA Substance Listings, and other similar requirements If you live by the values of excellence, passion, integrity, quality and sustainability, you will love working for Siegfried.

Candidates for this role are eligible for remote work under Siegfried's work from home policy.  The successful candidate can be located in either Pennsville, New Jersey or Grafton, Wisconsin

Further tasks and responsibilities:

• Prepare regulatory documentation for assigned products for submission to the regulatory agencies or customers
• Submit CMC Drug Substance Submissions, prepare eCTD files and transmit through regulatory on-line portals
• Ensure compliance to regulatory guidance's, regulations, as well internal policies
• Work with subject matter experts internally in a timely manner to respond to questions from health authorities
• Provide regulatory guidance to departments or project teams regarding development, evaluation or validation of drug substances
• Develop global regulatory strategies and execute product changes in close cooperation with global Regulatory Affairs
• Review and Assess Change Controls
• Submit FDA Site Registrations and Drug Substance & Product Drug Listings for all Siegfried globally
• Assist with gathering information for responses to deficiency letters, track responses with various experts within other company departments to ensure a timely response to FDA
• Provide technical support for Customer Service (e.g. act as a support role for customer requests for foreign sites for products that are being imported into the US)
• Imports/Customs: Review End Use Letters in a timely manner from customers for accuracy and ensure it meets FDA import requirements, assist with technical support for FDA in order to clear customs and avoid detentions/returns

• Education: BA/BS degree in chemistry, pharmacy, biology, or equivalent
• Language: Fluent in English
• Work experience: 5+ years in a similar position
• Industry experience: Experience in pharmaceutical environment including interactions with FDA. Knowledge of cGMP's is a must.
• Who we are looking for: We would like to welcome a colleague who is a team player and has outstanding communication skills. In addition, you are very conscientious and detail-oriented. This position requires someone who has a self-starter and initiator mentality.