Senior Associate, Regulatory Affairs (Labeling)

Schaumburg, IL, United States Full Time

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POSITION OBJECTIVE:           Responsible for the support of label creation, development and review, including assistance with submission, deficiency and commercially available labeling updates based upon partner or FDA requests.  


Essential Job Functions/Responsibilities

·      Responsible for the creation of commercial, submission and deficiency labeling with a focus on ensuring that all Regulatory, Quality and Manufacturing requirements are satisfied

·      Performs critical proofreading of label copy at all stages of the product life cycle

·      Ability to complete tasks related to label development, proofreading and copy review within specified timelines

·      Assists in the preparation and compilation of electronic submissions in eCTD

·      Examines and researches laws, regulations and guidelines governing the development/commercialization of drugs

·      May participate in project planning to ensure submission requirements and timing are in alignment with overall project timelines

·      Supports the preparation of documents as needed


Required Education & Qualifications

  • Bachelor’s degree in a scientific discipline (Chemistry, Microbiology/Biology, Pharmacy, PreMed or Nursing)

·      3-5 years direct pharmaceutical industry experience or work experience in a cGMP and/or FDA regulated environment. Regulatory, Labeling or Quality experience preferred.

  • Knowledge of the regulatory affairs function, preferably in a pharmaceutical or FDA-regulated industry
  • Demonstrated proofreading ability
  • Excellent working knowledge of Microsoft Office software (Microsoft Word and Excel) and Adobe Acrobat
  • Experience with pharmaceutical labeling in any capacity is preferred; experience with document comparison software a plus
  • Well organized with a passion for quality and an impeccable detail orientation
  • Able to work independently and within a team environment
  • Solid interpersonal (verbal and written) communication skills at all levels
  • Thrive in, and able to work in, a fast paced entrepreneurial environment



Athenex is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. 


Athenex is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please notify HR and let us know the nature of your request and your contact information

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