03 Oct
|
Aspiro Pharma
|
Hyderabad
03 Oct
Aspiro Pharma
Hyderabad
Roles and Responsibilities
- Ensure compliance with USFDA regulations for injectable products (sterile) and solid oral dosage forms.
- Develop, implement, and maintain quality systems to ensure product quality and regulatory compliance.
- Conduct audits of manufacturing facilities, laboratories, and other departments to identify areas for improvement.
- Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
- Provide training on Good Manufacturing Practices (GMP), cGMP guidelines, OSD requirements, sterility testing methods.
Desired Candidate Profile
- M.Pharma/M.Sc from a recognized university with 20-25 years of experience in pharmaceutical industry.
- Robust knowledge of QA/QC principles, USFDA regulations, injectables production processes.
- Experience in auditing procedures; ability to conduct internal audits independently.
📌 General Manager QA (Hyderabad)
🏢 Aspiro Pharma
📍 Hyderabad