Dera Bassi, Punjab, India
Not disclosed
On-site
Full Time
Company Description Nectar Lifesciences Ltd. (NLL) is a leading organization in the Indian Pharmaceutical Industry, ranked amongst the top midsized companies in India and among the top fore runners in the Bio-Pharmaceutical industry in Asia-Pacific. NLL has a strong global presence in API & Formulation business in almost 45 countries with state-of-the-art manufacturing facilities. The company prioritizes global standards of cGMP, Environment Health Safety (EHS), and has a highly skilled workforce at all levels. Role Description This is a full-time on-site role for a Regulatory Affairs Manager (APIs) at Nectar Lifesciences Limited located in Dera Bassi. The Regulatory Affairs Manager will be responsible for handling regulatory compliance, requirements, submissions, and maintaining quality systems on a global scale within the pharmaceutical industry. Qualification Bachelor or Master's with Chemistry Understanding of Regulatory Requirements and DMF, CEP, CADIFA, KDMF, JDMF, CDMF Submissions Show more Show less
India
None Not disclosed
On-site
Full Time
Company Description Nectar Lifesciences Ltd. (NLL) is a vital part of the fast-growing Indian Pharmaceutical Industry. Recognized as a top midsized Pharmaceutical company in India and a leading Bio-Pharmaceutical company in the Asia-Pacific region, NLL has a significant global presence. The company is involved in the API & Formulation business in around 45 countries and operates 11 state-of-the-art manufacturing facilities in Punjab and Himachal Pradesh. NLL is publicly listed with stocks traded on BSE and NSE, and has a wholly owned subsidiary in Portugal. Role Description This is a full-time, on-site role for a Production Injection Filling Operator based in India. The Production Injection Filling Operator will be responsible for operating machinery, ensuring quality control, and managing production lines. Daily tasks include monitoring equipment performance, maintaining operational efficiency, and adhering to safety and compliance protocols. The role also involves effective communication with team members and participating in training sessions to maintain high standards of production. Qualifications 10+2/ITI
Dera Bassi, Punjab, India
None Not disclosed
On-site
Full Time
DMFs & CEPs application CADIFA Application Annual Report - USDMFs Knowledge on ICH, PIC/s, EMEA guidance KDMFs, CDMFs, JDMFs compilation and submission Submission on CESP Portal Solicita Portal ESG (USFDA) Publishing and e-Validation
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