Description
This position is with an exciting small molecule oncology company, who just received approval from the FDA for their first drug. We are looking for someone who can perform internal and external GMP audits. The position will also require some knowledge of quality systems audits and maintaining responsibility for the audit schedule.Key Responsibilities:
- Perform internal and external GMP audits to ensure that quality systems are robust and in compliance with regulatory requirements.
- Maintain audit schedule to ensure quality oversight of CMOs, suppliers and internal functions.
- Prepare audit subject matter activities in support of partner and regulatory agency inspections.
Requirements:
- 4-5 years working experience in a GMP environment
- Lead auditing experience
- BS/BA degree in a related field
If you believe your background aligns with the requirements and responsibilities for this role, please apply and we will reach out to you shortly.
To find out more about Real please visit www.realstaffing.com