About Teva Pharma
Teva is a worldwide drug pioneer and the world's biggest nonexclusive prescriptions maker, focused on further developing wellbeing and expanding admittance to quality wellbeing arrangements around the world. Our workers are at the center of our prosperity, with partners in north of 80 nations conveying the world's biggest medication bureau to 200 million individuals consistently. We offer a particularly different arrangement of items and answers for patients and we've constructed a promising pipeline based on our center remedial regions. We are consistently creating patient-driven arrangements and altogether becoming both our nonexclusive and specialty medications business through interest in innovative work, promoting, business improvement and advancement. This is the way we further develop wellbeing and empower individuals to live better, better lives. Go along with us on our excursion of development!
Set of working responsibilities
Arranging, executing and investigating support during the execution of logical business related to Nitrosamines for the alloted Undertakings (~ 6) in a successful way founded on the given timetable to work with progress of the ANDA projects and partake in the worldwide discussion.
To perform and direct the group for the insightful strategy advancement, Technique Approval, Strategy Move, bunch investigation exercises for formative task. Autonomously with the elevated degree of Gross domestic product consistence
Support worldwide group in giving the essentials expected to the undertaking.
Support in Arranging, Checking on and endorsing the Instrument Capability and Adjustment exercises
Support Group in Quality related work, for example, Change Control, Research facility Examination, Deviation and so on.
Take part in getting ready/exploring Standard Test method, Sop's, Conventions, Report and other Quality related Records, rigorously sticking to the Quality consistence and as per GLP.
Set of working responsibilities
Team up with logical staff from ARD and FRD for arranging, Focusing on the insightful exercises connected with entries or administrative quarries
To guarantee that movements of every kind attempted are executed in the structure of GLP rehearses as well as great documentation rehearses and the current quality frameworks are stuck to.
Investigating of insightful instruments for challenges looked during everyday activities.
Lab consistence and information trustworthiness during everyday tasks.
Effectively partake in the execution of EHS framework/Strategy and guarantee the protected practices are follow during the execution of scientific exercises and severe adherence to the EHS frameworks of the site.
Fantastic abilities in the field of Writing Overview connected with the scientific strategy improvement connected with Nitrosamine Contaminations
Capabilities
MSc./M. Pharm. Logical Science 12-20 Years
Ph.D.- > 10 Years
Openings for Freshers in Regulatory affairs
Job Opening at Sarjen Systems Pvt. Ltd.
SME Regulatory Affairs
Qualification: B.Pharm / M.Pharm / Graduate in any paramedical field
Experience: 1 Years or above (Fresher can also apply)
Based at: Ahmedabad
Key Task :
1) Publish, major and complex routine/lifecycle management eCTD submission projects for EU, US, Canada and GCC.
2) SPL Preparation
3) eCTD software support and troubleshooting
4) Well aware to regulatory guidelines
5) Maintain working knowledge of internal and external publishing standards.
6) Knowledge of ICH and eCTD related specification/guidelines governing regulatory submissions (eCTD, NeeS, paper)
7) Aware of Technical systems like Adobe Acrobat, eCTD Validator etc.
Contact us at [email protected]