This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory.
Work both independently and as part of intra, inter-departmental teams to ensure that all work is completed in a timely manner to meet both business and quality standards.
Regular reporting in Envision. To maintain the desired call average per month and frequency of calls to be done as expected with respect to Dual Ranking of Customers. Call objectives should be managed to give focus on various Products as agreed.
Support DM Delivery Leads to maintain CDM specified systems and types of deliverables, milestone achievements, risks and mitigations and data transfer agreements, and other study administrative needs.
Master degree in any branch of Chemistry or Pharmaceutical chemistry, Pharmaceutical analysis, quality assurance.
02 years experience in analysis of ASUH drug using sophisticated instruments.
Ph.D. in Biochemistry, Microbiology, Biotechnology, Pharmacology, Life sciences. The candidate must have at least one research publication in SCI-indexed Journals.
B.Sc in Life Sciences, Microbiology, Biotechnology, Biochemistry, or any other relevant discipline from a recognized institution. OR M.Sc. with minimum 60% marks. With experience in size exclusion chromatography, western blotting and Flow Cytometry will be preferred.
Will be responsible for managing Discovery, Development projects end to end. Adept at managing project milestones, budget and stakeholders. Should have excellent communication skills. Must be a good negotiator and must have hands-on knowledge in MS Project, MS Excel.