Quality Assurance Officer Documentation – Quality Assurance | Bueno Salud Care India Private Limited | Chacharwadi, Ahmedabad, Gujarat, India
Bueno Salud Care India Private Limited is hiring a Quality Assurance Officer Documentation for its pharmaceutical manufacturing facility located in Chacharwadi, Ahmedabad, Gujarat, India. This full-time role is ideal for professionals with 2 to 4 experience in pharmaceutical quality assurance and documentation systems within the Pharmaceutical industry in India. The position focuses on maintaining quality documentation, ensuring compliance with GMP guidelines, and supporting internal quality audits. The selected candidate will work closely with production teams, regulatory affairs professionals, and quality control laboratories to ensure accurate documentation and regulatory compliance. Bueno Salud Care India Private Limited operates in the pharmaceutical manufacturing sector with strong emphasis on regulatory compliance, product quality, and process validation. This opportunity allows professionals to develop expertise in pharmaceutical quality systems and regulatory documentation while contributing to maintaining high-quality production standards.
Location
Chacharwadi, Ahmedabad, Gujarat, IndiaEmployment Type
Full-timeExperience Required
2 to 4Compensation & Benefits
Competitive salary package with opportunities to work within regulated pharmaceutical quality systems.About Bueno Salud Care India Private Limited
Bueno Salud Care India Private Limited is a pharmaceutical manufacturing organization focused on producing high-quality healthcare products while maintaining strict compliance with regulatory standards.Position Overview
The Quality Assurance Officer Documentation will manage pharmaceutical documentation systems and support quality compliance activities across manufacturing operations.Key Responsibilities
- Maintain GMP documentation and quality records.
- Prepare and review standard operating procedures.
- Support internal and external quality audits.
- Ensure documentation compliance with regulatory standards.
- Monitor batch manufacturing and quality records.
- Coordinate with production and quality control teams.
- Maintain document control systems.
- Support deviation investigation documentation.
- Assist in regulatory inspection preparations.
- Ensure data integrity within quality systems.
Required Skills & Competencies
- Knowledge of pharmaceutical GMP documentation systems.
- Experience with quality assurance documentation.
- Understanding of regulatory compliance requirements.
- Attention to detail and documentation accuracy.
- Quality audit and compliance awareness.
- Strong communication and coordination ability.
- Documentation control and record management skills.
- Problem-solving capability in quality systems.
- Understanding of pharmaceutical manufacturing operations.