Associate Director Quality Assurance (Good Laboratory Practice - GLP)
SciPro is partnered with one of the fastest growing Biotechs on the West Coast, with a large product portfolio & pipelines across multiple Therapeutics Areas.
This organization is currently searching for an experienced GLP Quality Expert to join their business as an Associate Director for Quality Assurance.
Responsibilities
- This is a business facing role where you’ll provide GLP focused Quality consultation cross-functionally to Research & Development departments
- You will be working with external vendors and laboratories to ensure GLP compliance with internal, domestic and international standards
- You will also be developing Quality strategy with focus on GLP as well as creating Quality focused metrics and KPIs, these will be reported back to Senior Leadership
Requirements
- Extensive experience in GLP Quality Assurance in the Pharmaceutical, Biotechnology and / or Medical Devices spaces
- Experience in management of External Vendors, both domestically and internationally
- Experience in creation and management of SOPs, hosting Internal & External Auditing activities as well as management of CAPAs and Deviations
- Minimum Bachelor’s in Life Sciences or Equivalent degree
If this is a role that interests you then please click respond through the LinkedIn apply function or send your resume over to J.
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