Quality Assurance (Process Validation, Qualification)

As an Officer/Executive in the Quality Assurance Department at a company located in Bavla, Ahmedabad, your role will involve the following responsibilities: **Role Overview:** You will be responsible for Process Validation and Qualification activities in the pharmaceutical manufacturing industry. **Key Responsibilities:** - Prepare standard operating procedures for various processes - Issue controlled formats to the concerned departments - Provide necessary documents for regulatory dossier submissions - Prepare protocols for Process Validation, cleaning validation, and hold time validation studies - Execute process validation, hold time validation, and cleaning validation activities - Review protocols for validation studies - Communicate critical process parameters and hold times to production - Collect samples, submit reports, and compile summary reports for validation studies - Issue validation protocols for hold time, cleaning, and process validation - Perform any other tasks assigned by the Head of Department **Qualifications Required:** - M. Pharma/B. Pharma/M. Sc degree - Exposure in the Parenteral background is a must The company emphasizes the importance of developing, implementing, managing, auditing, and maintaining GMP Quality systems. You will also be responsible for reviewing and approving SOPs, participating in internal audits, and reviewing Master Documents like BMR, Protocols, and Reports. If you are interested in joining our organization, please send your detailed resume to Recruitment@swiss.in.,