Company Overview

Ray Life Sciences Pvt. Ltd. is a leading pharmaceutical manufacturing company with a state-of-the-art injectable manufacturing facility located in Hubli, India. Backed by Mr. Anjan Roy, founder of RL Fine Chem, our aim is to manufacture the highest quality injectables for domestic and global markets. Our facility is designed to meet WHO and international cGMP guidelines. With our global presence, worldwide network, financial strength, and strong research focus, we are an attractive partner in the industry.

Job Overview

We are seeking a highly skilled and experienced Executive - Quality Assurance to join our team at Ray Life Sciences Pvt. Ltd. As an Executive - Quality Assurance, you will be responsible for ensuring that our manufacturing processes and products meet the highest quality standards. This is a mid-level position requiring 4 to 6 years of experience in quality assurance.

Qualifications and Skills

• Bachelor's degree in Pharmacy, Chemistry, or a related field.
• 4 to 6 years of experience in quality assurance in the pharmaceutical industry.
• Strong knowledge of WHO and international cGMP guidelines.
• Experience in injectable manufacturing and aseptic processing.
• Excellent analytical and problem-solving skills.
• Attention to detail and strong documentation skills.
• Ability to work effectively in a cross-functional team.
• Good communication and interpersonal skills.

Roles and Responsibilities

• Develop and implement quality assurance policies and procedures for our manufacturing processes.
• Monitor and evaluate the quality of raw materials, intermediates, and finished products through regular inspections and audits.
• Ensure compliance with WHO and international cGMP guidelines.
• Coordinate with cross-functional teams to address quality issues and implement corrective actions.
• Conduct root cause analysis and implement preventive measures for quality deviations and non-conformities.
• Prepare and maintain quality documentation, including standard operating procedures, batch records, and quality records.
• Manage deviations, change controls, and CAPA (Corrective and Preventive Action) processes.
• Participate in internal and external audits and ensure timely closure of audit findings.
• Provide training and guidance to staff on quality assurance practices and procedures.