Sr.Executive - Quality Control

Jamjoom Pharma; Jeddah; On-site; SAR 90,000 - 120,000; Full time

Job summary

A leading pharmaceutical company in Jeddah is seeking a Sr. Executive QC. The role is responsible for performing routine and non-routine analytical testing of raw materials and finished products, ensuring compliance with cGMP and internal quality systems. The ideal candidate will have 5-7 years of relevant experience and a Bachelor’s or Master’s degree in a science-related field. Strong analytical skills and knowledge of regulatory guidelines are essential. Join a fast-growing company focusing on quality assurance in pharmaceuticals.

Qualifications

• 5-7 years of relevant experience in Quality Control within a regulated pharmaceutical company.
• Sound knowledge of analytical techniques and pharmacopeial / In-house methods (USP, BP, EP, IP).
• Familiarity with regulatory guidelines (WHO, SFDA, USFDA, MHRA, EMA).

Responsibilities

• Perform routine and non-routine chemical analysis of intermediates, finished products and raw materials.
• Conduct stability studies and maintain records as per ICH guidelines.
• Collect and compile data for documentation of tests and prepare final reports.

Skills

Analytical techniques

Good communication

Teamwork

Problem-solving abilities

Education

Bachelor’s or Master’s degree in Chemistry / Biochemistry / Microbiology or B. Pharm / M. Pharm

Tools

HPLC

GC

UV

FTIR

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:

Sr. Executive QC will be responsible for routine and non‑routine analytical testing of raw materials, in‑process samples, finished products, and stability studies. The role requires ensuring compliance with cGMP, regulatory standards, and internal quality systems while supporting production timelines.

Responsibilities:

• To perform routine and non‑routine chemical analysis of intermediates, finished products and raw materials as per approved Specification and test method.
• To Conduct stability studies and maintain records as per ICH guidelines.
• To collect and compile the data for documentation of test performed and prepare the final reports accurately, in line with ALCOA+ principles and ensure data integrity.
• Operation, use, maintenance, and calibration of analytical instruments (HPLC, GC, UV‑Vis, FTIR, Dissolution, etc.)
• Maintenance & Daily checks of Analytical Balances and pH Meters.
• To maintain the reference standards, chemicals, reagents, Volumetric Solutions and solvents list and report any requirements of the laboratory to the supervisor.
• To maintain logbooks and record of all laboratory activities.
• Participate in analytical method transfer.
• Handling of deviations, OOS, OOT investigations, and implement CAPA in coordination with QA.
• Follow the safety and Hygiene system and policy of the company.
• cGMP / GLP Compliance in QC Laboratory, and to maintain good documentation practices.
• Any other QC analytical work as and when required.

Qualifications:

• Bachelor’s or Master’s degree in Chemistry / Biochemistry / Microbiology or B. Pharm / M. Pharm.
• 5 –7 years of relevant experience in Quality Control within a regulated pharmaceutical company.
• Sound knowledge of analytical techniques and pharmacopeial / In‑house methods (USP, BP, EP, IP).
• Hands‑on experience with analytical instruments such as HPLC, GC, UV, FTIR.
• Familiarity with regulatory guidelines (WHO, SFDA, USFDA, MHRA, EMA,).
• Strong documentation skills with adherence to data integrity principles.
• Good communication, teamwork, and problem‑solving abilities.
• Exposure to LIMS/Chromatography Data Systems (e.g., Empower) is an added advantage.