Puerto Life Sciences Private Limited
Location: Neemrana, Rajasthan (Sterile Facility)
Designation: Executives & Officers
Qualification: B.Pharma, M.Pharma & M.Sc (Microbiology/Chemistry/Biotechnology)
Production
Skills Required:
•Expertise in sterile compounding processes, including CIP/SIP systems, component preparation, and sterilization.
•Hands-on experience in aseptic operations, media filling, sterilization processes, and area monitoring.
•Ability to troubleshoot and manage challenges in aseptic manufacturing environments.
Quality Assurance
Skills Required:
•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.
Quality Control
Skills Required:
•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.
Experience:
1 to 5 years of experience in sterile manufacturing
Please share the required details such as your resume, current CTC and notice period at: [email protected]
