Job Description

Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region. The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions. Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the company.

Role Summary

Responsible for the analysis of API and excipients, method development, product evaluation, developmental stability studies, method validation, and method transfer for finished products and APIs. Accountable for laboratory instruments calibration and proper record keeping as per the group leader’s instructions. Ensures compliance with GMP standards within the laboratory and assists in Environmental Health and Safety (EHS) assessments.

Responsibilities

• Perform analytical method development, validation, and method transfer activities for Tablets, Capsules, Ophthalmic, Topical, and Soft Gel dosage forms in accordance with ICH and regulatory guidelines.
• Develop stability-indicating methods for Raw Materials, In-Process Samples, and Finished Products.
• Execute method validation studies including specificity, precision, accuracy, linearity, robustness, ruggedness, LOD, and LOQ as per approved protocols.
• Perform analytical testing using instruments such as HPLC/UPLC, GC, UV-Visible Spectrophotometer, Dissolution Apparatus, and other laboratory equipment.
• Conduct method transfer activities to Quality Control or other manufacturing sites and provide technical support during transfer.
• Prepare, review, and maintain analytical documents including protocols, reports, STPs, specifications, and standard operating procedures (SOPs).
• Evaluate analytical data, interpret results, identify out-of-specification (OOS) / out-of-trend (OOT) results, and participate in investigations.
• Ensure compliance with cGMP, GLP, Good Documentation Practices (GDP), and regulatory requirements from USFDA, MHRA, WHO, and other authorities.
• Support regulatory submissions by preparing analytical sections and responding to regulatory queries, if required.
• Perform routine calibration and ensure proper maintenance of analytical instruments.
• Coordinate with cross-functional teams such as Formulation Development, Quality Assurance, and Production for smooth project execution.
• Maintain laboratory safety, cleanliness, and adherence to company quality policies.
• Assist in troubleshooting analytical issues and contribute to continuous improvement initiatives within the department.
  

Qualifications

• Bachelor’s or Master’s Degree in Chemistry or Pharmacy.
• Minimum 3–5 years of experience in Analytical Development within the pharmaceutical industry.
• Strong knowledge and competency in Analytical Chemistry.
• Basic knowledge of HPLC and dissolution test apparatus techniques.
• Good written and verbal communication skills.
• Ability to work efficiently and complete assigned tasks within deadlines.