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.
Vacancy Details:
Job Description:
Puerto Life Sciences Pvt. Ltd.
our mission to deliver world-class sterile
Join our mission
WE’RE HIRING
Puerto sterile products
Department: Quality Assurance
Designation: Sr. Executive
Experience: 5+ Years QA
Designation: Officer
Experience: Up to 4 years
Job Responsibilities: Ensures GMP compliance by reviewing BMR /BPR, overseeing line clearance, IPQA, deviation handling, and document control. Coordinates audits, manages QMS elements Up to 4 Years like CAPA/change control, and supports training, validation, and cross-functional compliance activities.
Designation: Executive – RA
Experience: 4+ Years
Job Responsibilities: Responsible for compiling, reviewing, and submitting regulatory dossiers (CTD/eCTD) for domestic and international markets. Coordinates with cross-functional teams to ensure timely approvals, license renewals, and regulatory compliance with health authorities.
How to Apply?
PLEASE SHARE THE REQUIRED DETAILS SUCH AS YOUR RESUME, CURRENT CTC AND NOTICE PERIOD AT: hr@puerto.in
SEEKING CANDIDATES WITH STERILE INDUSTRY EXPERIENCE ONLY
