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QA Associate in Thousand Oaks, CA at Apex Life Sciences

Date Posted: 11/19/2018

Job Snapshot

Job Description


Responsibilities:

  • Review and approval of printed clinical labels, finished clinical pack inspection, expiration date calculation and batch record review.
  • Generation and compilation of quality data and reports (e.g. lot track/trace, deviations).
  • Assist with procedure reviews and initiation of deviation reports.

Qualifications:

  • Must have experience with GMP processes and documentation.
  • Must be able to methodically and meticulously inspect printed materials for print quality defects, clinical product components (e.g. syringes and vials) for physical defects, and batch record documentation for accuracy and completeness.
  • Must be able to work in a team with shifting priorities and shifting responsibilities, such that the team members must be confident verbal communicators able to discuss responsibilities, divide them, reassess them, and potentially reassign them throughout the day or week.

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.




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