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2.0 - 6.0 years
0 Lacs
andhra pradesh
On-site
As a Quality Assurance Officer in the chemical industry, your role involves ensuring that products and processes meet established quality standards and regulatory requirements. You will be responsible for developing and implementing Quality Management Systems (QMS) such as ISO-9001, conducting audits, monitoring testing, analyzing data, and resolving quality issues. Your key responsibilities will include: - Maintaining documentation - Conducting Root Cause Analysis - Implementing Corrective and Preventive Actions (CAPA) - Performing Out of Specification (OOS) and Out of Trend (OOT) investigations - Collaborating with cross-functional teams - Operating and calibrating laboratory equipment - E...
Posted 6 days ago
5.0 - 9.0 years
0 Lacs
palghar, maharashtra
On-site
Role Overview: As a Raw Material Quality Control Analyst, your main responsibility will be to ensure that all raw materials (API & excipients) used in manufacturing are sampled, tested, and released according to pharmacopeial/in-house specifications and regulatory standards before they are utilized in production. You will play a crucial role in maintaining the quality and integrity of raw materials used in pharmaceutical manufacturing processes. Key Responsibilities: - Receive and verify raw material intimation from the warehouse. - Conduct GMP-compliant sampling using appropriate tools and in classified environments (if applicable). - Properly label samples and maintain sampling logbooks. -...
Posted 1 month ago
3.0 - 7.0 years
0 Lacs
hyderabad, telangana
On-site
As a Pharma Subject Matter Expert (SME) Trainer, you will be responsible for training candidates in various aspects of Quality Control (QC), Cell Culture Techniques, and Laboratory Procedures. Your role involves providing hands-on experience in analytical testing, microbiological testing, and pharmaceutical laboratory operations. It is essential to educate candidates on method validation, stability testing, and data integrity while ensuring compliance with FDA, USP, and cGMP regulations. Additionally, you will train individuals in utilizing HPLC, GC, UV-Vis, FTIR, PCR, ELISA, and Spectroscopy techniques. Your responsibilities include conducting mock interviews, assisting with resume preparat...
Posted 1 month ago
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