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.Actively participate in project teams/ meetings/ networks.
5.Meet quality, quantity and timelines in all assigned projects.
6.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
7.Provide efficient and robust processes for the analysis of DS/ DP under adequate guidance from more experienced team members.
8.Provide scientific and technical guidance. Coach team members as needed. 9.Interact/ collaborate with other groups/ functions to facilitate transfer of knowledge of DS/ DP
13.Give guidance to team members and work according to appropriate SOPs, GLP, GMP, OQM, HSE, ISEC and Novartis guidelines.
14.Contribute to risk analyses and/ or peer review and process challenge meetings.
15.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. 16.Actively contribute to team goals.
17.Report and present scientific/ technical results internally and contribute to publications, presentations and patents.
18.Evaluate new lab equipment and prepare CAR and URS if applicable 19.Contribute to maintenance of infrastructure/ equipment and required investments.
Salary: Not Disclosed by Recruiter
Industry:Medical / Healthcare / Hospitals
Functional Area:Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology
analytical msc hplc validation scientific writing gmp registration glp instrumentation chromatography
Desired Candidate Profile:
UG: B.Pharma – Pharmacy
PG:M.Pharma – Pharmacy
Doctorate:Any Doctorate – Any Specialization, Doctorate Not Required
MSc, MPharm or equivalent Good knowledge of English (oral and written English 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.
Novartis Healthcare Pvt. Ltd.
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes us one of the most rewarding employers in our field.