Looking for Research Associate at leading Phrama Co.

Job Description:

• Independently perform the experiments and document the observations within the timelines meeting the quality requirements for assigned projects
• The candidate will be responsible for Analytical Method development and validation for Excipients and finished dosage forms under guidance of ADL incharge
• Troubleshoot experiment and instrument errors
• Operate and maintain the different analytical equipment’s like HPLC, Dissolution tester, weighing balance, pH meter, pipettes, DT apparatus, UV spectrophotometer, Friability apparatus.
• Preparation and validation of SOPs for instruments and analytical processes
• Preparation of analytical protocols and scientific reports
• Use knowledge and expertise to interpret and document the experimental data
• Perform work under GLP practices and maintain documentation of the records as per the SOPs
• Test all FnD samples as per stability schedule and share ADL reports to FnD team

Technical Knowledge/ Skills Requirement:

• MSC Chemistry/M.Pharm in QA with 1-2 years exp or B.Pharm with 3+ years exp
• Knowledge of HPLC and dissolution apparatus is a must for 6 months-1 year
• Practical knowledge of pharmaceutical development processes and dose forms
• Well versed with ICH, OECD GLP and all regulatory guidelines for analytical method development and their validation.
• Hands-on experience of equipments like HPLC, Dissolution tester, weighing balance, pH meter, pipettes,
• DT apparatus, UV spectrophotometer, Friability apparatus.
• Excellent skills in collection of data and documenting the observations in the laboratory notebooks

Behavioral Skills

• Excellent relationship building & interpersonal Skills.
• Motivated, Teamwork and spirit of co-operation
• Understanding of analytical issues
• Working closely with customers and partners to ensure correct analytical solution to problem.
• Willing to work flexible hours
• Good communication and listening skills