Puerto Life Sciences Hiring For QA/ QC/ Production Dept
Designation: Assistant Manager/Manager
1) Department : Quality Assurance
Qualification : B Pharma/M Pharma
Skills Required for Sterile Manufacturing :
•Expertise in risk assessment, investigations, CAPA implementation, and effectiveness checks.
•Thorough knowledge of SOPs, change control, and compliance monitoring for sterile environments.
•Strong understanding of batch record reviews, protocol preparation, and regulatory compliance.
•Proficient in handling deviations, internal/external audits, and ensuring GMP adherence in sterile conditions
•Experience in MQA operations and global sterilization standards verification
2) Department : Production
Qualification : B Pharma/M Pharma
Skills Required for Sterile Manufacturing :
•Expertise in sterile compounding processes, including CIP/SIP systems, component preparation, and sterilization.
•Hands-on expenence in aseptic operations, media filling, sterilization processes, and area monitoring
•Ability to troubleshoot and manage challenges in aseptic manufacturing environments.
•Strong leadership in overseeing sterile production operations while ensuring adherence to GMP standards.
3) Department : Quality Control
Qualification : MSc-Microbiology/ Chemistry/Biotechnology
Skills Required for Sterile Manufacturing :
•Strong understanding of both analytical and microbiological testing in sterile manufacturing
•Proficiency in analytical testing techniques (HPLC, GC. UV, etc.) for product quality and regulatory compliance.
•Expertise in environmental monitoring (viable/non-viable), bioburden, and sterility testing
•Knowledge of stability studies, release testing, and pharmacopoeial requirements for sterile products.
•Strong leadership to oversee both microbiological and analytical QC teams, ensuring adherence to GMP standards
Please Share The Required Details Such As Your Resume, Current Ctc And Notice Period At:
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| Puerto Life Sciences Hiring For QA/ QC/ Production Dept |
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