Senior Scientist Information

Job Details

[The logo is protected from the company]

(0) (0)

Novartis Healthcare Pvt Ltd

Novartis (NYSE: NVS) is a world leader in the research and development of products to protect and improve health and well-being. The company has core businesses in pharmaceuticals, vaccines, consumer health, generics, eye care and animal health. Headquartered in Basel, Switzerland, Novartis employs nearly 115 000 people in over 140 countries worldwide to help save lives and improve the quality of life. The Group is present in India through Novartis India Limited, listed on the Mumbai Stoc... Read More

Address	Sandoz House Shivsagar Estate Dr Annie Besant Road Worli, Mumbai India
Website	www.novartis.in/
Holding	No Holding Details

View Company Page

Apply to job

Senior Scientist

1.Actively participate in project teams/meetings/networks. 2.Meet quality, quantity and timelines in all assigned projects. 3.Design, plan, perform, interpret and document DS/DP related analytical activities including release/stability testing, method development/validation etc. under minimal guidance from more experienced team member 4.Provide efficient and robust processes for the analysis of DS/DP under adequate guidance from more experienced team members. 5.Provide scientific and technical guidance. Coach team members as needed. 6.Interact/collaborate with other groups/functions to facilitate transfer of knowledge of DS/DP 7.Give guidance to team members and work according to appropriate SOPs, GLP, GMP, OQM, HSE, ISEC and Novartis guidelines. 8.Contribute to risk analyses and/or peer review and process challenge meetings. 9.Generate scientific documents to hand over to internal and/or external partners and actively support generation of international registration documents under adequate guidance from more experienced team members. 10.Actively contribute to team goals. 11.Report and present scientific/technical results internally and contribute to publications, presentations and patents. 12.Evaluate new lab equipment and prepare CAR and URS if applicable 13.Contribute to maintenance of infrastructure/equipment and required investments. 1.Actively participate in project teams/meetings/networks. 2.Meet quality, quantity and timelines in all assigned projects. 3.Design, plan, perform, interpret and document DS/DP related analytical activities including release/stability testing, method development/validation etc. under minimal guidance from more experienced team member 4.Provide efficient and robust processes for the analysis of DS/DP under adequate guidance from more experienced team members. 5.Provide scientific and technical guidance. Coach team members as needed. 6.Interact/collaborate with other groups/functions to facilitate transfer of knowledge of DS/DP 7.Give guidance to team members and work according to appropriate SOPs, GLP, GMP, OQM, HSE, ISEC and Novartis guidelines. 8.Contribute to risk analyses and/or peer review and process challenge meetings. 9.Generate scientific documents to hand over to internal and/or external partners and actively support generation of international registration documents under adequate guidance from more experienced team members. 10.Actively contribute to team goals. 11.Report and present scientific/technical results internally and contribute to publications, presentations and patents. 12.Evaluate new lab equipment and prepare CAR and URS if applicable 13.Contribute to maintenance of infrastructure/equipment and required investments. Desired Profile MSc, MPharm or equivalent Good knowledge of English (oral and written). .1. Successfully demonstrated a minimum of 4 years relevant experience with Phd. or 8+ years with MSc/MPharm in the pharmacetical industry 2. Strong experience in Dissolution and HPLC methods execution and stability assessment of dosage forms. 3. Working knowledge in the use of the following instrumentation: GC, titrimeters, UV/NIR/IR spectroscopy. Advanced computer skills: LIMS, chromatography data acquisition systems, MS office 4. Effective team player, able to work in a flexible, dynamic working environment 5. Good knowledge of cGMP requirements 6. Good oral and scientific writing skills 7. Good multi-tasking with good time management skills. Experience 8 - 9 Years Industry Type Pharma / Biotech / Clinical Research Role Clinical Research Associate/Scientist