About Company:
Puerto Life Sciences is a leading pharmaceutical manufacturer based in Neemrana, Rajasthan, specializing in Large Volume Parenterals (LVP) and Small Volume Parenterals (SVP). Our state-of-the-art facilities produce high-quality injectable formulations, adhering to stringent international standards such as GMP. With a mission to enhance patient care through innovative and effective parenteral solutions, we serve major clients including Cipla, Glenmark, and Mankind. Our capabilities range from high-volume production to customized batches, ensuring flexibility and precision for diverse market demands. Committed to quality and efficiency, Puerto Life Sciences is poised for expansion, aiming to meet the evolving needs of the global healthcare market and maintain our position at the forefront of pharmaceutical manufacturing.
Website
http://puertolifesciences.com
Vacancy Details:
Job Description:
WE ARE HIRING
Puerto Life Sciences Private Limited Neemrana, Rajasthan (Sterile Facility)
Designation: Executives & Officers
Qualification: B. Pharma, M. Pharma & M. Sc (Microbiology/Chemistry/Biotechnology)
Department: Production
Skills Required : Expertise in sterile compounding processes, including CIP/SIP systems, component preparation, and sterilization.
With Experience of 1 to 5 Years: Hands-on experience in aseptic operations, media filling, sterilization processes, and area monitoring.
for Sterile Manufacturing: Ability to troubleshoot and manage challenges in aseptic manufacturing environments.
Department: Quality Assurance
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.
Department: Quality Control
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.
PLEASE SHARE THE REQUIRED DETAILS SUCH AS YOUR RESUME, CURRENT CTC AND NOTICE PERIOD AT: hr@puerto.in
