We are Rasan Pharmaceuticals, an Iraqi Pharmaceutical manufacturer of sterile products, located in Sulaymaniyah, Kurdistan Region of Iraq, we are one of Faruk Investment Group (FIG)s private company that engages in manufacturing, testing, commercializing, packaging, and distribution of diverse lines of high quality of sterile injectable products, such as standard intravenous solutions in both Polyolefin bags and Polypropylene bottles, in addition to new lines of eye drops and medicament injectable solutions in glass vials and Oral solutions in polypropylene bottles, using state-of-the-art technology.

The facility is designed to meet the highest international standards and all our products are manufactured in accordance with the latest international standards, conforming to all USFDA, cGMP regulations in addition to local authority regulations. The well-being of people inspires our work and we are committed to producing the best and the highest quality in our field 

Stability & Methodology R&D Section head


1. To prepare all the requirements needed for building the analytical R&D laboratory, hence to ensure the adequate resources (i.e. equipment, staff, consumables, facilities, documents, etc.) to meet the department and companys goals.

2. Works closely with product development team to develop product formulation.

3. Ensures the timely review, compilation, interpretation and communication of results

4. High experience in modern analytical techniques like spectrophotometric techniques (UV-VIS, IR, etc.) and chromatographic techniques (TLC/HPTLC, HPLC, UPLC, and GC).

5. Responsible for Method Development and Validate the stability-indicating assay method for new products for QC.

6. Providing technical support to QC laboratories, and assisting in investigations

7. Prepare and review SOPs, Specifications, Test methods, Validation Protocols and Reports

8. Resolve technical issues with analytical methods and instrumentation

9. To initiate stability programs for the R&D trials and final developed products.

10. Prepares the assessment of summarized experimental data of all investigations pertaining to a product file that is to be submitted for registration.

11. Prepares the requests needed for new laboratories or laboratory equipment and instrumentation to serve expanding operational requirements.

12. Reviews professional journals and scientific papers to keep abreast of changes in processing methods of analysis and stability regulations.

13. Prepares & presents the planning and development of survey instruments, guidelines and procedures to collect required data.

14. Collect data of stability product and investigation OOS

15. Ensuring the new product analysis results meet the product specification

16. Creates product files & necessary paperwork for registration and export.

17. Investigates problems relating to products in stability chambers during analysis

18. Investigates any out of trend to stability products

If you are interested please send your CV to the email address: info@rasanph.com

Post a Comment