Aryan Singh

B.Pharm graduate with professional experience in the Pharmaceutical Industry, specializing in Quality Control of Finished Goods Products. Skilled in performing analytical testing, in-process quality checks, finished product analysis, and laboratory documentation in compliance with GMP, GLP, and SOP guidelines. Experienced in handling and operating instruments such as HPLC, UV Spectrophotometer, Dissolution Apparatus, pH Meter, and other QC laboratory equipment.

Adept at maintaining accuracy in testing, supporting batch release processes, and ensuring product quality and regulatory compliance. Strong analytical, problem-solving, and teamwork abilities with a commitment to maintaining high pharmaceutical quality standards.

Officer - Mediforce Healthcare Pvt. Ltd - Ponta Sahib, Himachal Pradesh

(2026-05)

• Performed routine quality control testing of finished pharmaceutical products as per approved specifications, standard test procedures (STPs), and pharmacopoeial requirements (USP, IP, BP).
• Conducted analysis of finished dosage forms including tablets and capsules using UV-Visible Spectrophotometer.
• Performed dissolution testing of oral solid dosage forms using Dissolution Test Apparatus (USP Apparatus I & II) and evaluated results against established specifications.
• Prepared analytical solutions, standard solutions, and reagents according to approved procedures.
• Ensured proper operation, calibration verification, and routine maintenance of laboratory instruments including UV Spectrophotometer and Dissolution Apparatus.
• Reviewed analytical data for accuracy and compliance with quality standards before reporting results.
• Assisted in Out-of-Specification (OOS), Out-of-Trend (OOT), and laboratory investigation activities.
• Maintained compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and data integrity requirements.
• Participated in method verification, instrument qualification, and laboratory audits.
• Performed sampling, testing, and release activities for finished products within specified timelines.

Chemist - Swift Life Sciences Pvt. Ltd - Dehradun, Uttarakhand

(2024-10)

• Prepared and maintained analytical reports, certificates of analysis (COA), and laboratory documentation in accordance with GMP and data integrity requirements.
• Conducted testing using analytical instruments such as HPLC, UV-Visible Spectrophotometer, FTIR, and Dissolution Apparatus.
• Ensured proper sampling, testing, and release/rejection of raw materials according to pharmacopeial standards (IP, BP, USP).
• Followed Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory guidelines during all QC activities.
• Maintained proper documentation including SOPs, logbooks, and test records to ensure audit readiness.
• Maintained adherence to ALCOA+ principles for data integrity and documentation practices.
• Conducted assay, related substances, dissolution, content uniformity, moisture content, and identification tests for pharmaceutical products.
• Prepared and standardized volumetric solutions, reagents, and mobile phases according to analytical procedures.
• Performed sampling, analysis, and release activities for raw materials and finished products following SOPs and GMP guidelines.

Internship - HFA Formulation Pvt. Ltd

• Successfully completed Industrial Training Programme in HFA Formulations Pvt. Ltd.

Bachelor of Pharmacy - Pharmacy - Shree Dev Bhoomi Institute of Education Science and Technology (2021 - 2025)

12th - Royal International School (2019 - 2021)

10th - The Visionrease School (2017 - 2019)