About company

SimSon Pharma Limited, a renowned name in the pharmaceutical sector, has built a high reputation as a complete solution provider in the contract research arena. We are leading manufacturer and supplier of pharmaceutical Reference materials like Drug working standard, Drug impurity standards, Drug metabolites, and Stable Isotope Labelled compounds. Our expertise in this area has made us one of the most trusted companies in the industry.

We are the front runner in manufacturing complicated Drug impurity standards or Reference materials and the complete solution provider in identifying, synthesizing, and qualifying any Unknown impurity. we are one-stop solutions for Chemical Development, Formulation development, Analytical development, and Regulatory services.

SimSon Pharma Limited, not only synthesizes and supply molecules but also provides a cost-effective & innovative approach to help companies achieve success. We work closely with our clients for understanding their requirements and offer them time-bound solutions.

Company name- Simson Pharma Limited

Position: QA/QC Officer

Website: https://www.simsonpharma.com/

Job Location: Vasai/Dahisar

Experience: Freshers /0-1

Qualification: M. Pharm, M.Sc. organic chemistry, PhD in organic Chemistry

Area of Expertise: HPLC, GC, UV, Mass, HNMR, IR, COA, MS Office, CAPA

:

Raw Material Analysis,



Finished Product/Formulation Analysis.

Experience in HPLC, Assay, Related substance, GC, FTIR, KF & Potentiometer.

To Prepare and Check Certificate of Analysis for Raw Materials, Intermediates, and Finish Products

Support the Technical Dept for Market complaints review.

Good Documentation Practice.

Mail Communication & Drafting.

MS- Office

COA reading and Documentation10.Basic understanding of CAPA

Roles & Responsibilities:

Prepare Quality Documents - BPR, SOPs, Logbooks.

Update the list of Equipment, Vendors, Instruments, SOPs.

To assign the batch for dispatch as per the customer requirement and plan the dispatch in coordination with production, stores, and quality control.

To segregate, file, store, and maintain the quality systems-related records in good condition.

To review the in-process, intermediate, raw material, packing material, and finished goods.

To Prepare and Check Certificate of Analysis for Raw Materials, Intermediates, and Finish Products.

To issue the labels, seal, and fastener and maintain the stock.

To keep the control sample after completion of analysis and update the related document.

Skills

Valuable communication

Ms. Office

Attention to Detail

Time Management

Problem-Solving

Analytical Thinking

📌 Officer - Testing services (Mumbai)
🏢 Simson Pharma
📍 Mumbai