Quality Control Associate

The Quality Control Associate will be responsible for conducting in-process, finished product and stability testing associated with the Adaptimmune clinical trial material.  This could include technology / method transfer of existing methods from outside laboratories.
 

  • 50% In-process, finished product and stability testing of clinical trial material
  • 20% Method / Technology Transfer of existing methods into the Adaptimmune QC Lab
  • 20% Validation, verification and maintenance of quality control equipment
  • 10% Maintenance of Quality Control Protocols, SOP’s and Test Methods

QUALIFICATIONS & EXPERIENCE

Required
  • Five years working in a GMP quality control laboratory
  • Proficient knowledge of GMP regulations including USP and EP testing requirements
  • Experience conducting time critical testing of in-process and finished product to meet clinical trial needs.
  • Ability to prepare data trending reports, and to author, review and maintain test methods, qualification protocols, SOPs and reports
  • Assist in conducting laboratory investigations and of prepare deviations and CAPAs as needed

Desirable
  • Five years working in a GMP quality control laboratory.
  • Ability to work on assigned projects independently with limited supervision.
  • Familiarity with flow cytometry, ELISA, endotoxin testing

SKILLS & COMPENTENCIES
  • Five years experience working in a GMP quality control laboratory
  • Knowledge of GMP regulations including USP and EP testing
  • Technical writing skills for drafting equipment and laboratory standard operating procedures

Desirable
  • Knowledge of flow cytometry testing, ELISA and Endotoxin testing

Open Date: November 2, 2018
Close Date: December 2, 2018
Location: USA - Philadelphia, Pennsylvania
 
Compensation:
Contact:
Attachment: N/A


Our vision is to advance the impact of cytometry in meeting current and emerging challenges in the life, biomedical, and physical sciences.
 

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