• Issuance and retrieval of Authorized documents (viz. Formats, Logbooks) to concerned department personnel.
• Prepare and review of IPQA related documents.
• Ensure every employee follows GDP.
• Line clearance and verification for various production activities and dispatch as per procedures.
• Ensure to follow the sampling plan in the respective areas.
• Verification of logbooks in the respective areas.
• Segregations and filling of executed batch documents received from concerned department.
• Review of Batch records and Preparation of batch review checklists and batch release certificate.
• To perform daily walkthroughs in the respective areas.
• Basic knowledge on the Electrical/Electronics components.
• Ensure the Quality Standards are followed across the manufacturing site
• Good Communication Skills.
• Excellent data collection and analysis skills.
• Good Knowledge in relevant regulatory standards.
   

Preferred candidate profile

Male Candidates - Pharma Industry/Manufacturing Industry

Perks and benefits

Health Insurance

ESI & PF

Transportation Facility

Bonus yearly

Role: Quality Assurance - Other

Industry Type: Medical Devices & Equipment

Department: Quality Assurance

Employment Type: Full Time, Permanent

Role Category: Quality Assurance - Other

Education

UG: B.Tech/B.E. in Biomedical, Diploma in Electrical, Electronics/Telecommunication

Key Skills

• quality assurance
• production
• supervision
• manufacturing