CURRICULUM-VITAE

Pritam Sharma
Correspondence address
Batail (Bhambla), Bhambla, Baldwara
Mandi (Himachal Pradesh)- India
contact number - +91 - 9805177670
e-Mail id – [email protected]
Analytical QC chemist with 5+ years of experience in the QC group of pharmaceutical company as well as chemical
industries. Working in a challenging environment, making best use of my skills and contribute significantly to the
organization’s development. Self-motivated, detail-oriented, cooperative team player, eager to learn. Excellent
interpersonal and communication skills demonstrated through effective teamwork, a professional attitude and
motivation to produce high quality work.

EDUCATIONAL QUALIFICATION: -
● M.Sc. Organic Chemistry from Bahra University Shimla hills Solan Year: - 2017
● B.Sc. from Govt. Degree College, Sarkaghat (H.P University) in June 2015.

JOB PROFILE: -
● Worked in compliance with GMP, FDA and ICH requirements.
● Practical knowledge of IP, USP and British Pharmacopoeia & Performed analysis of pharmaceuticals raw
materials as per IP, BP, USP as well as chemicals.
● Analytical soft skills: MS Office, Power Point & Internet surfing, SAP logon Pad, LIMS EMPOWER-3 FR-4,
Chromeleon 6.8 & 7.2, Open lab CDS and Lab solution software for HPLC (make- waters Corp. Agilent, Shimadzu
& Thermofischer).
● Excellent command in using and troubleshooting HPLC, IC (Metrohm), GC, GC-HS, Malvern Particle Sizer,
UV/Visible spectrophotometer, Potentiometer, Karl Fischer Titrator, Dissolution Apparatus, Dis-integration
Tester, Muffle furnance, Melting and boiling point apparatus, MDI-ACS, MDX Auto Actuator, Analytical balance,
UV Chamber (TLC) pH meter, Polarimeter and chemical techniques.
● Capable of handling multiple assignments under high pressure and consistently meeting tight deadlines.

EMPLOYMENT HISTORY: -

Company: Morepen Laboratories Limited (Masulkhana-Solan, H.P.)

Designation: QC Chemist (Trainee)
Duration: August 2017 to July 2018 (US-FDA Audit faced for Montelukast Sodium USP)
• Performed analytical tests & sampling of RM Chemical, in-process and FG API.
• Analysis of Raw material, Bulk Product, Semi finished, Finished Product API.
• Calibrated and maintained laboratory instruments developed standard operating procedures and review test
results. Collected data and completed report summaries.
• Prepared test reports and maintained test records. Participated in problem solving and troubleshooting and
direct report to the QC Manager.

Company: FDC Limited (Baddi Solan, Himachal Pradesh)

Designation: QC Chemist Officer
Duration: Feb 2019 to June 2020
• Performed analytical tests : Assay, Content Uniformity, Identity, Impurities, testing of oral solid, liquid &
suspension dosage finished product for release and stability studies using HPLC(Waters 2489, Shimadzu,
Thermofischer & Agilent), GC, GC-HS UV/VIS, (Perkin Elmer & Shimadzu), TLC, Friability (Make- Lab
India), Tablet Dis-integration Apparatus (Make- Lab India), Sonicator (Make- Labtronics), Analytical Balance
(Digital) and chemical Techniques in accordance with established GMP's, GLP's and SOP's, performed
dissolution test on solid and suspension dosage forms using extreme competence.
• Documented, interpreted and reported test results within the scheduled time interval.
• Notified department supervisor/manager regarding omissions, incomplete testing results or other irregularities.
• Worked within the laboratory in a team environment; assisted with QC initiatives; actively participated
 in QC projects and team meetings.
• Authored methods, Documentation of all incoming material, stability protocols, stability reports, method
equivalency protocols and other technical documents.
• Kept a detailed record of all experiments, analysis of Raw material, Bulk Product, Semi finished, Finished
Product & Packing material, collected data and completed report summaries.
• Verified the integrity and traceability of all incoming material data generated and reported.
• Trained junior chemist to perform HPLC, GC, GC-HS UV/VIS Spectrophotometer and Dissolution USP I, II,
analysis and result interpretation.
• Experienced in identification and troubleshooting of analytical and minor instrumental problems Analysis of
In-process samples, Stability batches and exhibit batches of Solid Oral Dosage forms by IP, USP, BP and In-
House Methods.

Company: Glenmark Pharmaceuticals Limited (Baddi Solan Himachal Pradesh)

Designation: QC Chemist Officer
Duration: Oct 2020 to Nov 2021
• Calibrated and maintained laboratory instruments developed under standard operating procedures and
reviewed calibration results. Prepared calibration reports and maintained calibration records of all instruments.
• Participated in problem solving and troubleshooting and direct report to the QC Manager. Preparation of
Standard solutions and standardizations them time to time.
• Collection of external calibration records, preventive maintenance record and reports to laboratory manager
as required. keep records of training imparted to QC person time to time and same for new joiner.
• Maintaining and monitoring of chemicals, glassware and spare parts for laboratory equipment. Coordinating
with the process departments and Control Room in providing reports in time.
• Maintaining Reference impurities, reference standard, working standard (IP, BP, USP & Inhouse) & in line
records of LC, GC column (procurement through SAP).
• Accountable for adopting the ALCOA+ (attributable, legible, contemporaneous, original & accurate)
principles
• Knowledge of QMS (OOS, OOT, CAPA Incidence, Deviation and Change Control).
• Responsible for ensuring that laboratory work areas maintain high standards of housekeeping and meet
requirements such as 5S, Laboratory management. (Reference standards, impurities, column, Chemicals,
logbooks etc.)
• Knowledge of GMP ICH Q7 and other regulatory requirements relevant to an analytical environment required.

Company: XL Laboratories PVT LTD (Bhiwadi Rajasthan)

Designation: QC Chemist Officer
Duration: Feb 2022 to Mar 2023
• Developed and validated methods for drugs on HPLC, UV/VIS Spectrophotometer and Dissolution
Apparatus.
• Performed Method transfer on HPLC, UV/VIS spectrophotometer and Dissolution Apparatus USP I & II.
• Reviewed validation documentation, including stability protocols, raw data and summary reports for
equipment qualification, process and cleaning validation to ensure compliance.
• Kept a detailed record of all experiments, analysis of Raw material, Bulk Product, Semi finished, Finished
Product & Packing material of Diagnostic Products, collected data and completed report summaries.
• Verified the integrity and traceability of all incoming material data generated and reported
• Maintained validation documentation, including stability study protocols, raw data and summary reports.
• Method validation (Assay, Dissolution, RS) as per ICH Q2 guideline and regulatory agencies by technique
HPLC, GC & UV, Experience in method transfer and verification/validation.

Company: SRF LTD (Dahej, Gujarat)

Designation: Junior Officer QC – JE
Duration: March 2023 to On-going

• Performing analytical tests like Assay, Identity, Impurities, testing of finished product for release and stability
studies using HPLC(Agilent), GC, GC-HS UV/VIS, (Perkin Elmer & Shimadzu), FT-IR, Analytical Balance,
pH meter, TDS meter (Digital) and chemical Techniques (titration) in accordance with established GMP's,
GLP's and SOP's.
• Maintaining 5S throughout the analysis, during documentation and laboratory environment and it cleanliness.
PERSONAL DETAILS: -
● Name: - Pritam Sharma
● Date of Birth: - 01 April 1993
● Marital Status: - Married
● Language proficiency: - English and Hindi
● Nationality: - Indian
DECLARATION: - I hereby declare that information furnished by me is true to best of my knowledge and
belief and that nothing material has been concealed.

(Pritam Sharma) Date: Place: