Responsible for analyzing medicine costs and feasibility for their organizations. tasked with analyzing data to verify that research has been completed and pharmaceutical development is on the right track, and also help evaluate business opportunities based on products on the market and supply-and-demand numbers. Also analyze statistics to find correlations between different products and their effectiveness, and work closely with sales and marketing departments to share important project information and reach all company goals in a timely manner. Help conceptualize market trends and preferences according to survey feedback, and work well with other analysts to develop strategies for distribution and increasing products' effectiveness.Use market intelligence to conduct regional tests of how products perform, as well.Use a variety of technologies to help expand business opportunities and identify segments which aren't covered by competitors. Develop schedules and forecasts to help minimize risk and maximize sales efforts.Implement customer feedback and multitask effectively to increase efficiency in the research and development stages. Organized and pay close attention to detail to find data to support their claims and help company objectives, and participate in product meetings to brainstorm new ideas to save costs and resources.

Quality Control Analyst I performs various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods and ensure compliance with established standards. Conducts and validates various biological and chemical quality control (QC) assays. Being a Quality Control Analyst I compiles, interprets, and documents statistical data from testing processes to either confirm compliance with established quality standards or identify deviations. May be responsible for establishing specifications for conducting assays and writing standard operating procedures. Additionally, Quality Control Analyst I typically requires a bachelor's degree. Typically reports to a supervisor or manager. The Quality Control Analyst I work is closely managed. Works on projects/matters of limited complexity in a support role.

Assist Production Manager in achieving required output. Responsible for production activities in the plant in accordance to codes of Good Manufacturing Practice (GMP).Responsible for all aspects of product, development activities which include upgrading of products quality, process validation and trouble-shooting.To liaise with other departments in day-to-day operation.
Manage and prioritize production operationImprove and enhance production operations and attain high quality in products.
Allocate work, supervise employees and control production wastagesInspect the quality of boxes and packing.
Coordinate with production manager and plan manufacturing process.
Plan production schedules and draft operational manuals.
Ensure complete availability of raw and packing materials.
Plan weekly, and monthly production target.
Instruct and educate employees on safety measures.
Monitored production activities and ensured compliance with GMP.
Maintained product quality and safe working environment.
Controlled production process and supervised employees.
Maintained hygiene of the production area.
Got production equipments cleaned and serviced at regular intervals.
Maintained records of stocks and production process.
Provided safety gears and apparels to employees and ensured they used them.


Quality Control Analyst I performs various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods and ensure compliance with established standards. Conducts and validates various biological and chemical quality control (QC) assays. Being a Quality Control Analyst I compiles, interprets, and documents statistical data from testing processes to either confirm compliance with established quality standards or identify deviations. May be responsible for establishing specifications for conducting assays.

Learning in Pharmacy
Patient's prescription
Drug-drug interactions
Monitoring safe use of medicine
Dosage Regimen Monitoring