Strong expertise in formulation development for different dosage forms (Solid, Liquid, Ophthalmic, Semisolid, mDPI, Softgel, Injectables, etc.).
Manufacture lab-scale batches for process improvement, quality improvement, and new source development.
Experienced in process optimization and validation; provide training to junior colleagues.
Perform formulation development and process validation activities for different dosage forms.
Prepare stability protocols, finished product specifications, process validation protocols, product development reports, and SOPs.
Coordinate Technology Transfer and Product Life Cycle Management activities.
Compile manufacturing documents for scale-up, submission, and validation batches, and prepare reports.
Manufacture scale-up, submission, and validation batches in coordination with other departments.
Conduct manufacturing process validation activities.
Age At least 22 years Advanced knowledge in MS Suite will be preferred.Strong decision-making skills with the ability to work independently and collaboratively.
https://bdjobs.com/h/details/1504816
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