Quality CDMO
Website:
qcdmo.com
Job details:
Company Description
Quality CDMO (Quality Contract Development and Manufacturing Organization) is committed to delivering high-quality pharmaceutical solutions. Our organization brings together chemists and scientists to address complex issues within the pharmaceutical industry. With a focus on innovation and teamwork, we turn abstract ideas into practical solutions, while maintaining our core values of quality and attention to detail. At Quality CDMO, we pride ourselves on creating value for our clients, contributing to a healthier society, and upholding a strong tradition of excellence.
Role Description
This is a full-time, on-site Quality Assurance Professional role based in Ahmedabad. The professional will ensure compliance with all regulatory and quality standards during the development and manufacturing processes. Key responsibilities include reviewing manufacturing and testing protocols, conducting audits, identifying quality issues, implementing corrective actions, and collaborating with cross-functional teams to maintain a robust quality assurance system.
Qualifications
- Proficiency in quality assurance processes, regulatory compliance, and quality management systems
- Strong documentation, auditing, and analytical skills
- Knowledge of pharmaceutical development, manufacturing protocols, and industry standards
- Effective problem-solving, team collaboration, and communication skills
- Bachelor’s degree in Pharmacy, Chemistry, or a related field
- Experience with GxP (Good X Practices), validation processes, and quality audits
- Attention to detail and ability to ensure adherence to stringent quality standards
- Experience in the pharmaceutical or related industries is preferred
Click on Apply to know more.