Deputy Manager Quality Assurance – Quality Assurance | Fountomics Lifesciences Pvt Ltd | Hyderabad, Telangana, India
Fountomics Lifesciences Pvt Ltd is seeking experienced professionals for the role of Deputy Manager Quality Assurance at its pharmaceutical operations in Hyderabad, Telangana, India. This full-time position is ideal for candidates with 5 to 8 experience in pharmaceutical quality assurance within the Pharmaceutical industry in India. The role involves overseeing quality management systems, reviewing manufacturing documentation, and ensuring compliance with regulatory guidelines and Good Manufacturing Practices. The selected candidate will collaborate with production teams, regulatory affairs specialists, and quality control laboratories to maintain high quality standards across pharmaceutical manufacturing processes.
Location
Hyderabad, Telangana, IndiaEmployment Type
Full-timeExperience Required
5 to 8Compensation & Benefits
Salary range: 5 to 8 with opportunities to work in pharmaceutical quality systems and regulatory compliance operations.About Fountomics Lifesciences Pvt Ltd
Fountomics Lifesciences Pvt Ltd is a pharmaceutical organization engaged in the development and manufacturing of pharmaceutical formulations and healthcare products.Position Overview
The Deputy Manager Quality Assurance will oversee quality assurance operations, monitor regulatory compliance, and support pharmaceutical manufacturing quality systems.Key Responsibilities
- Review batch manufacturing and packaging documentation.
- Ensure compliance with GMP and regulatory guidelines.
- Manage quality assurance activities within production.
- Support internal and regulatory audits.
- Investigate deviations and implement corrective actions.
- Maintain quality management documentation.
- Coordinate with production and quality control teams.
- Ensure compliance with pharmaceutical regulatory standards.
- Support validation and qualification activities.
- Promote continuous quality improvement initiatives.
Required Skills & Competencies
- Knowledge of pharmaceutical quality assurance systems.
- Understanding of GMP regulations.
- Documentation and compliance management skills.
- Analytical problem-solving capability.
- Strong communication and leadership skills.
- Attention to detail in regulatory compliance.
- Team collaboration and coordination skills.
- Ability to manage quality investigations.
- Regulatory documentation expertise.