Aurore Life Sciences, established in 2017, is a leading manufacturer of Active Pharmaceutical Ingredients (APIs) and intermediates, offering high-quality, affordable bulk drug solutions to over 55 countries worldwide. With a pure-play focus on APIs and intermediates, Aurore is a fully backward-integrated pharmaceutical company dedicated to delivering to all regulated markets globally.
At the heart of our business model is complete backward integration, ensuring control over every stage of production—from raw materials to the final API. This streamlined process guarantees not only an uninterrupted supply chain but also enhances product consistency, quality, and cost-efficiency. By reducing our reliance on external suppliers, Aurore Life Sciences offers customers a reliable and uninterrupted supply of essential APIs and intermediates, positioning us as the preferred supplier of choice in the industry.
Our diverse product portfolio comprises over 60 APIs, more than 122 Drug Master Files (DMFs), and over 100 intermediates. Supported by state-of-the-art manufacturing facilities, we meet the evolving needs of pharmaceutical companies worldwide.
Aurore Life Sciences strictly adhering to cGMP guidelines. Our manufacturing units have undergone numerous inspections by regulatory bodies such as USFDA, HPRA, AGES, EMEA, EDQM, COFEPRIS, PMDA, TGA, WHO-Geneva, KFDA, ANVISA, and certifications like ISO 9001:2008 and OHSAS 18001:2007. This commitment to quality and compliance underscores our dedication to delivering safe, effective, and reliable pharmaceutical ingredients.
With cutting-edge facilities, a strong emphasis on innovation, and sustainability embedded in our core values, Aurore Life Sciences continues to earn its reputation for excellence in the industry. We remain committed to making essential medicines accessible globally while partnering with leading pharmaceutical companies to meet the healthcare needs of people worldwide.
DATE AND TIME:
2nd November , 9.30 AM – 2.00 PM
Aurore Pharmaceuticals pvt ltd, Plot No 34,36,38,39,40,49,50 and 51, Phase IV,IDA,Jeedimetla,Quthubullapur mandal , Mechal District,Telangana-500055
Contact – CHAMARTI VENKATA RAMAIAH
1 – 5 years
2-3.5 Lacs P.A.
Job description
Execution of the Batch production records like MBPRs, Cleaning BPRs etc Indent and receipt of raw materials and general items Plan the Batch movement as per schedule and maintain the records as per standard operating procedures. Follow the validations as per protocols (Process /Cleaning) Ensuring the raw materials and intermediates storage and handling as per defined procedure/ Instruction.Role:
Production & Manufacturing – OtherIndustry Type:
Pharmaceutical & Life SciencesDepartment:
Production, Manufacturing & EngineeringEmployment Type:
Full Time, PermanentRole Category:
Production & Manufacturing – Other
Education:
B.Sc in Chemistry
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