Job Responsibility •To follow safety rules in the premises according to the company norms •Monitoring of DP, RH and temperature in aseptic processing area •To maintain the BMRs and other log books in the aseptic processing area as per cGMP
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated sterile manufacturing environment, with a specific focus on injectable dosage form production.
Job Description SummaryTo supervise and coordinate aseptic filling and isolator operations for sterile injectable products, ensuring production targets are achieved while maintaining compliance with cGMP, aseptic practices, data integrity, and global regulatory requirements (USFDA, EU GMP, MHRA, WHO,
Role Objective A key objective of this position is to lead and govern the Quality function at the manufacturing site, ensuring uncompromised product quality, patient safety, and compliance with global regulatory requirements (USFDA, EU-GMP, MHRA, WHO-GMP,
Designation - Quality Assurance Manager Location - Nepal Ensure quality of product as per company standards at optimal cost. Responsibilities Overall responsibility for implementing and reviewing Food Safety and Quality Management System. To ensure and comply
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since 1998 , with