Pooja Sharma

Assistant Professor - CERT group of institution

(2023-08)

Delivered a range of high-Positively engaged in the professional development of teaching, learning and assessment quality and inclusive teaching and support learning activities.
Assessed the work and progress of students and provide them with constructive feedback.
Proactively identified ways to improve performance through teaching design, delivery and by obtaining and analyzing feedback.
Developed and applied innovative approaches to improving the learning environment, teaching, assessment, and feedback methods. Contributed to course development and the development of new programmers of study in an inclusive way.
Prepared various kinds of reports by evaluating and grading the students based on their assessment.
Kept in touch with current trends by reading the latest articles published in different magazines or other relevant literature.
Planned and organized for the availability of different study materials and laboratory equipment.
Developed and taught undergraduate and graduate courses in pharmacy practice, pharmacology, and medicinal chemistry.
Mentored and advised students on research projects, theses, and career development.

QC Executive - Akums drugs and pharmaceutical

(2017-03 - 2021-01)

Nature of Duties and Responsibilities

Execution of Analytical Method validation activities for drug products as per the regulatory requirements.
Execute routine Analytical Research activities of drug products.
Establishing In-house systems and procedures to ensure cGLP practices & regulatory requirements for analytical activities at In-house R&D facility.
Trouble shooting related to Testing methods, Stability studies, test results and designing of additional experimentations as necessary
Execution & coordination for Analytical method transfer activities of drug products.
Calibration of the Analytical instruments as per the master calibration schedule.
Technical assessment & Analysis of drug substances (API) for projects execution.
Review & clearance of technical documents leading to dossier batches executions and registrations.
Preparation and review of Specifications, Method of analysis procedures and Analytical development reports.
Preparation and review of analytical protocols and reports (Analytical method validation, Method feasibility, Analytical method transfer).

QC Officer - Synokem pharmaceutical pvt ltd - Haridwar

Perform analysis with a practical understanding of the test procedure and instrument operation
Work under direction provided by supervisor and Other duties as assigned
Maintain required level of training needed to perform a GMP task
Organize work schedule to complete assigned tasks efficiently and on schedule
Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results
Maintain accurate record of analysis and perform documentation to company standards
Notify manager immediately of nonconforming data or unexpected occurrences
Prepare test solutions, volumetric solutions, and samples used in analysis
Other duties as assigned by management as needed
Support regulatory inspections and audits
Support of various stability study protocols and execution of study tests
Preparation of laboratory reagents and samples; operation of instruments; data analysis; preparation of analytical reports; notebook documentation
Lift up to 30 pounds on occasion
Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials.

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