About this role
Job Description
Primary Job Responsibilities:
- 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 Biopharmaceutics
Doctorate in Biotechnology or Biopharmaceutics
Competencies
Collaboration
Customer Centricity
Developing Talent
Innovation & Creativity
Process Excellence
Result Orientation
Stakeholder Management
Strategic Agility
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