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QA Associate (Batch Record, Regulatory Support) in Allentown, PA at Apex Life Sciences

Date Posted: 11/28/2018

Job Snapshot

Job Description


  • Review and approve Batch Records to ensure compliance with SOPs and FDA regulations.
  • Organize large amounts of data and information
  • Assist the regulatory department with any technical writing or batch recording as necessary


  • Minimum of a High School Diploma; Bachelor’s degree or equivalent in related field preferred.
  • 2+ years’ experience in a regulated manufacturing industry in a Quality role.
  • Demonstrated ability to work independently, handle multiple tasks simultaneously, and meet critical timelines;
  • Knowledge of cGMPs and FDA Regulations

For immediate consideration, please email your resume to with the subject 'QA Associate'

EEO Employer

Apex is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at 844-463-6178.