Gracure Pharmaceuticals Ltd.
Website:
gracure.com
Job details:
Company Description Gracure Pharmaceuticals Ltd. is a research-driven, forward-looking pharmaceutical organization focused on delivering world-class, affordable medicines. The company is fully integrated across Research and Development, Manufacturing, Sales, and Marketing of diverse finished dosage forms. Guided by strong values and high quality standards, Gracure emphasizes “Quality Products… On Time In Full” for international markets. Its commitment to care and cure drives continuous growth and the ability to meet demanding requirements of global partners.
Role Description This full-time, on-site Senior Executive Quality Control – Quality Management System role is based at Gracure’s facility in Bhiwadi. The role involves overseeing and maintaining the Quality Management System (QMS), including documentation control, SOP creation and revision, and ensuring compliance with cGMP and regulatory guidelines. The Senior Executive will coordinate internal audits, support external and regulatory inspections, and drive CAPA (Corrective and Preventive Actions) and change control processes. Day-to-day tasks include reviewing batch records, monitoring quality metrics, supporting process and method validation activities, and collaborating with cross-functional teams to resolve quality issues. The role also requires training team members on quality procedures and contributing to continuous improvement initiatives in quality operations.
Qualifications
- Strong knowledge of Quality Management Systems, including documentation control, change management, and CAPA processes.
- Experience with cGMP, GLP, and regulatory compliance for pharmaceutical manufacturing, including audit and inspection readiness.
- Proficiency in quality control activities such as batch record review, deviation handling, and support for process and method validation.
- Ability to analyze quality data, prepare reports, and implement continuous improvement initiatives in manufacturing and packaging operations.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related scientific discipline.
- Relevant experience in pharmaceutical Quality Control or Quality Assurance, preferably in a regulated, international market-focused environment.
- Strong communication, coordination, and documentation skills, with the ability to work effectively in cross-functional teams on-site.
- Attention to detail, problem-solving mindset, and readiness to take ownership of quality processes and training activities.
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