Come grow with Advarra’s Quality Auditing Team! We are seeking additional Quality Auditors in Asia Pacific, South America, Europe, Australia, New Zealand, and Canada to support the quality and compliance needs of our clients. Consultants needed for GxP audits – GCP, GMP, GLP/GcLP, IT/CSV.
Consultants will professionally apply working knowledge and expertise in clinical research, quality assurance and other diverse areas to effectively provide service and project deliverables. Consultants must have experience conducting independent audits to include audit preparation, execution and remediation. Opportunities are remote and onsite based on client requirements.
The Consultant should have the following:
• Minimum of ten (10) years of Quality Assurance and/or GxP (e.g., Clinical, Manufacturing, Laboratory, etc.) experience in pharmaceutical, biotech, medical device, and other applicable life science industries
• Minimum of five (5) years of Quality Assurance experience and knowledge in Clinical, Laboratory, Manufacturing, and/or Pharmacovigilance experience
• Strong skill in interacting with clients
• Ability to work effectively with internal and external stakeholders
• Must be able to communicate effectively, both orally and in writing; write and edit written materials, explain complex information clearly and concisely in English is required.
Our Consultants support our clients with following:
- Global Engagements (as applicable and agreed)
- Investigator Site Audits
- CRO Audits
- Vendor Audits
- GCP
- GMP
- GLP
- GcLP
- IT/CSV
If you are interested in joining our Quality Auditing Consulting team, please respond with your CV to the designated person below:
Asia Pacific – send email and CV to sherr.kollath@advarra.com
South America, Europe, Australia, and New Zealand – send email and CV to benjamin.sager@advarra.com
Canada – send email and CV to monica.bounds@advarra.com