01Responsibilities
Product characterization using LC/MS for biosimilarity studies. Training related to advanced LC-MS applications and DQA SOPs. Planning of experiments. Drafting and/or review reports and presentations on experimental data and scientific outcomes for CMC / RA for dossier submission, method qualification, assessing biosimilarity etc. Guiding and mentoring team members Sample preparation, LC-MS workflows and data interpretation. Support cross-functional analysis such as impurity characterization. Method Development, Qualification and report preparation. Procurement related to new instruments. To assess new technologies to enhance in-house scientific and technological capabilities. Comply to quality aspects (CAPA, CC, Deviation). Comply to safety norms and attend safety training. To ensure compliance to all KAVACH and EHS Policies. Any responsibility advised by the superior from time to time. Work Experience 5 to 10 years.Education Masters in Biotechnology or BiopharmaceuticsDoctorate in Biotechnology or BiopharmaceuticsCompetencies CollaborationCustomer CentricityDeveloping TalentInnovation & CreativityProcess ExcellenceResult OrientationStakeholder ManagementStrategic Agility .
