Lead process development for new immediate release and modified release solid oral dosage to facilitate technology transfer.
Plan scale-up / down batches in manufacturing area and oversee the batch executions with the responsible project scientists / mfg team.
May lead and/or Collaborates with multidisciplinary teams to resolve complex product / process development issues and respond to internal and external audits.
Generate accurate, reliable data by following established procedures and practices. Record, tabulate, summarize, interpret, report and publish study results.
Develop and maintain department standard operating procedures.
Co-ordination with QA/QC/Store/Eng./manufacturing department for smooth functioning of MSTG activities.
To do the documentation as per cGMP/SOP/BMR/Qualifications as per GDP.
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