M.Sc/ Mpharm/ PhD; Deep understanding of various analytical tools and supporting software like Empower, OpenLab CDS, LabSolutions. And Chromeleon; This role focuses on analytical method development for route scouting, process development, and the scale-up of various crop protection products. The ideal candidate will have a skill set to operate and develop methods on GC-MS, LC-MS, and UPLC/UHPLC.
M.Pharm / MSc. in Analytical Chemistry / Organic Chemistry; Execute the Isolation projects. Carry out the isolation, purification of known and unknown impurities, compounds by preparative HPLC and characterization of molecules using various analytical techniques. Involve in project acceptance.
The job requires review of documents related to DMF submission against predefined checklists and submission to various agencies globally. Should keep the all the regulatory database up to date. Candidate must possess do it right the first-time approach with proven track record.
Exposure to OSD Manufacturing operations like Granulation, Compression, Coating, Pellet coating, Capsule filling, Primary Packing and Secondary Packing. Expertise in e-BPR and e-log will be added advantage.
Good knowledge of Tablet & Capsule, Coating, Granulation, Compression, Good command on QMS & Documentation, IPQA, Qualification. Having good knowledge for scale up, technology transfer and site transfer. Candidates currently in Production and QA may also explore career opportunity in FTT for faster professional growth.
Senior scientist-II will work on isolation, purification of known and unknown impurities/compounds by preparative HPLC and characterization of molecules using various analytical technique and Analytical Method Development for in process samples received from synthetic Lab.
He, she will be responsible for providing Therapeutic Area workstream leads with administrative support on pre-defined projects. The Project Manager will set and develop the operational aspects of the project, develop, and monitor timelines, milestones and project metrics and is responsible for managing the projects from an operational perspective from the development and initiation phases through implementation and completion within scope provided by Medical Directors who remains responsible and accountable for the project content.
To ensure that the products are manufactured and stored as per appropriate documents in order to obtain the required quality. To ensure that the production records are reviewed as per current procedures.