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8.0 - 10.0 years
0 Lacs
hyderabad, telangana, india
On-site
Summary Primary Location: Warsaw, Poland Other Locations: Mumbai, India; Hyderabad, India Relocation Support: This role is based in Warsaw, Poland. Novartis is unable to offer relocation support: please only apply if accessible. Join Novartis in shaping the future of quality excellence! As a Senior QA Expert ESO, you'll ensure that all Novartis products manufactured by external suppliers meet international GMP standards and regulatory requirements. Acting as the Single Point of Contact, you'll drive compliance, foster strong partnerships, and lead continuous improvement initiatives that make a real impact on patient safety and global quality standards. About The Role Key Responsibilities Act...
Posted 2 weeks ago
7.0 - 11.0 years
0 Lacs
karnataka
On-site
Role Overview: You will be overseeing manufacturing and production operations at Dr. Reddys Laboratories Ltd., ensuring compliance with regulatory audits and managing equipment, process validation, and various activities related to production and manufacturing. Key Responsibilities: - Handle line operations, specifically production and manufacturing activities like CIP (Cleaning-in-place), SIP (Sterilizing-in-place), and batch manufacturing. - Manage equipment such as Steam Sterilizer, Dry heat sterilizer, HVAC (Heating, Ventilation, and Air Conditioning), water system, compressed air, Nitrogen system, etc. - Perform process validation for Sterilization, Washing, Aseptic filling, and cleanin...
Posted 1 month ago
5.0 - 10.0 years
0 Lacs
surat, gujarat
On-site
Role Overview: You should have a minimum of 5-10 years of experience in Production, R&D, or formulation development activities. As a Production Manager, your primary responsibilities will include proposing and implementing recommendations to enhance efficiency, safety, and quality, supporting new product development projects, controlling production activities, maintaining high standards of housekeeping and cleanliness, monitoring yield losses, minimizing manufacturing costs, reviewing batch records and documents, preparing and reviewing SOPs, providing on-the-job training, coordinating with QA and QC for validation and in-process checks, and ensuring the maintenance of cGMP standards. Key Re...
Posted 2 months ago
7.0 - 10.0 years
7 - 10 Lacs
Visakhapatnam, Andhra Pradesh, India
On-site
We are looking for a candidate to oversee manufacturing and production operations, managing equipment, process validation, handling change controls, deviations, incidents, and ensuring compliance with regulatory audits. Responsibilities include creating SOPs (Standard Operating Procedure), providing training, and applying expertise. Roles & Responsibilities You will be responsible for handling line operations, specifically production and manufacturing activities like CIP (Cleaning-in-place), SIP (Sterilizing-in-place), and batch manufacturing. You will be responsible for handling equipment like Steam Sterilizer, Dry heat sterilizer, HVAC (Heating, Ventilation, and Air Conditioning), water sy...
Posted 5 months ago
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