Multiple Posts in Nectar Lifesciences | Require in FR&D, AR&D, QA, QC, CR&D, Production, Business Development

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Nectar Lifesciences Ltd (NecLife) is a 200 million US$ integrated pharmaceutical organization, offering comprehensive range of Cephalosporin Active Pharmaceutical Ingredients and Finished Dosage Forms. The development and manufacture of quality intermediates, bulk actives have been critical to our success to become one of the largest manufacturers of cephalosporin range of products and delivering innovative and affordable products to domestic as well as international markets. NecLife has tactically positioned itself in the global pharmaceutical industry. It has developed sustainable production systems to manufacture highest quality pharmaceutical products meeting diverse requirements of its customer base in over 45 countries worldwide.

1. Department: Formulation Research & Development
Position/Designation: AM/DM/Manager/Sr. Manager
Preferred experience: 6-12 years
Roles and Responsibilities: Candidate will be responsible for designing of strategies for formulation developing of varied dosage forms. He will be responsible for designing the plan and review formulation optimization to justify the additives used in the process,  for evaluating the specifications desired for product developed as required by the various regulatory markets and inline with the official monographs and he will also be responsible for monitoring of Pre-exhibit / Test batches for the Process for accuracy and analyze the critical parameters at different stages of the process for finalization of Product specifications.

2. Department: Formulation Analytical Research & Development
Position/Designation: RA/RS
Preferred experience: 2-5 years
Roles and Responsibilities: Candidate must have good exposure of analysis of finished products i.e tablets, powder for injections, powder for injections, raw material, exciepients by different analytical techniques like HPLC, UV, FTIR etc. Development & Validation of SA, RS & dissolution by HPLCs

3. Department: Quality Assurance
Position/Designation: Manager/Sr. Manager/AGM
Preferred experience: 8 - 15 years
Roles and Responsibilities: Candidate must have good exposure in both sterile and oral API manufacturing units (reputed firms preferably manufacturing Cephalosporins / Penems etc.) Thorough knowledge on ICH / EUDRALEX Guidelines and its effective implementation. Faced regulatory bodies (US / Europe etc.). Thorough knowledge on Qualifications / Validations and cleaning validations

4. Department: Quality Control           
Position/Designation: Sr. Manager/ AGM/ DGM
Preferred experience: 8 - 15 years
Roles and Responsibilities: Candidate should be responsible for over all functioning of QC. To overview the testing and release of raw material, packing materials & drug intermediates. To overview the testing of APIs as per approved specifications & STPs. Responsible to provide required documentation support to RA for timely submission of dossiers, product registration & drug licenses.

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