Quality Assurance Associate

Highly Competitive
  1. Permanent
  2. Good Manufacturing Practice (GMP), Good Clinical Practice (GCP)
  3. United States
Philadelphia, Pennsylvania
Posting date: 26 Jun 2019
QA,MJ,24041_1561547307

A leading biotechnology research organization is seeking to recruit a Clinical Development Director. Based in Pennsylvania, this establishment is renowned for their focus on developing next-generation gene transfer vectors and their application in the treatment of a variety of acquired and inherited diseases. This position offers an exciting opportunity to work with a company that is riven by the unmet needs of patients with genetic diseases.

Job Responsibilities:

  • Auditing GLP laboratories.
  • Performing reviews on Batch Records.

Skills and Requirements:

  • -Bachelor's degree.
  • +5 years of experience in QA.
  • Experience working in GLP environment.
  • GxP experience preferred.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Mary Jacobs at +1 267-477-4800 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI-MJ1

#Compliance/Quality

close