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Job Description & How to Apply Below
Lead analytical activities for biosimilar programs with focus on HPLC, CE, and SoloVPE.
Supervise 2–3 team members (RAs, interns, trainees) including daily task oversight.
Ensure structured training, onboarding, and competency development for junior staff.
Perform method execution, troubleshooting, data review, and scientific interpretation.
Support method qualification for HPLC, CE, and SoloVPE techniques.
Contribute to documentation including MQP, MOA, MQR, specifications, and analytical similarity studies.
Maintain compliance with SOPs, data integrity, and regulatory expectations.
Collaborate across functions to support biosimilar development timelines.
Qualification:
MSc/ MTech/MPharm
Preferred Expertise:
Hands-on experience in analytical techniques for biopharmaceuticals (6–8 years).
Knowledge of advanced characterization tools:
Mass analysis, CD, Flr, DSC, MALS (added advantage).
Strong documentation, review, and data interpretation skills.
Prior experience mentoring or supervising junior analysts.
Position Requirements
10+ Years
work experience
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