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@manikantaveesam
M.S. Pharm formulation scientist with 5 years' experience in oral solid and liquid drug development.
I am an M.S. Pharmacy professional with five years of hands-on experience in early- to late-stage drug product development for oral solids and liquids, including analytical characterization and stability evaluation.
I have led formulation and process development, executed formulation trials, supported technology transfer to manufacturing scale, and prepared CMC documentation for regulatory submissions for US, EU, and China markets.
I work cross-functionally with analytical development, regulatory affairs, QA/QC and manufacturing, contribute to problem-solving and continuous improvement, and have participated in patenting and vendor coordination to accelerate product development timelines.
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Work history, roles, and key accomplishments
Hetero Labs Limited
Nov 2020 - Present (5 years)
Led formulation and process development for multiple oral solid and liquid dosage forms for US and EU markets, supporting tech transfer and regulatory submissions while troubleshooting scale-up issues across projects.
Delexcel Pharma
Jul 2019 - Nov 2020 (1 year 4 months)
Developed IR and MUPS tablet formulations for the China market, executed formulation trials and analytical evaluations, and prepared documentation to support manufacturing and regulatory requirements.
Degrees, certifications, and relevant coursework
Master of Pharmacy, Pharmaceutical Technology
2017 - 2019
Grade: 8.1 CGPA
Completed M. Pharmacy in Pharmaceutical Technology with hands-on training in formulation and drug product development; graduated with 8.1 CGPA.
Bachelor of Pharmacy, Pharmacy
2012 - 2016
Grade: 6.8 CGPA
Completed B. Pharmacy with coursework in pharmaceutical sciences and practical training in drug formulation; graduated with 6.8 CGPA.
Software and tools used professionally
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