POSITION OBJECTIVE: Support Quality Assurance (QA) activities at our Dunkirk, New York facility. Activities to include issuance and review of regulated documents, ensure processes and products are in compliance with current Good Manufacturing Practices and 21CFR 210/211, and provide QA support for internal Quality Systems.

This position is based on site in our Dunkirk, New York facility. Remote work is not an option for this role.

Essential Job Functions/Responsibilities

  • Generation of controlled documents in support of APS operations, including but not limited to Batch Record documents/forms, specifications and logbooks   
  • Provide Final QA review, approval and release for executed Batch Records and other Doc & Data    
  • Maintain department readiness for internal and external audits
  • Assist in the Internal Audit Program
  • Provide quality system/GMP training in support of organization
  • Maintain training requirements and records within electronic systems
  • Process and support Doc & Data creation and updates
  • Provide compliance review of general quality system elements (e.g., change control, work orders, working documents, etc.)
  • Maintain current and archived versions of controlled documents/records (paper and electronic)
  • Assist in retrieval and compilation of metric data
  • Build and maintain collaborative working relationships within the organization
  • Effective communication throughout all facets of the organization
  • Follow and solicit good manufacturing and documentation practices
  • Support QA compliance activities as needed
  • Support Quality Management System continual improvement initiatives
  • May perform other duties as assigned.

Required Education & Qualifications

  • Bachelor's degree or higher preferred; background and experience will be considered in lieu of Bachelor's degree  
  • Minimum of 3 years of related work experience in a regulated environment - pharmaceutical or related industry preferred
  • Knowledge of Good Manufacturing Practices (GMP)
  • Experienced with use of current office software (e.g., Word, Excel, PowerPoint, etc.)
  • Knowledge and experience with use of electronic quality management systems preferred

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.

Apply for position now

Are you legally authorized to work in the United States?
Will you now or in the future require sponsorship for employment visa status (e.g. H-1B, O-1, E-3, L-1, or TN)?
By checking the box below, I attest that all information contained in this application is true and accurate, and I understand that any false statement or omission is grounds for rejecting my application, or for termination of employment if I receive an offer of employment.
How did you hear about this opportunity with Athenex?
Do you have any relatives currently employed by Athenex?
Do you have previous work experience in a regulated industry?
Do you have a high school diploma or equivalent?
Do you have knowledge of Good Manufacturing Practices (GMP)?
Do you have experience with the use of electronic quality management systems?