Julphar
Specialist - Quality Control
- Permanent
- Ras Al Khaimah, United Arab Emirates
- Experience 2 - 5 yrs
Job overview
Date posted
16/09/2025
Location
Ras Al Khaimah, United Arab Emirates
Salary
AED 15,000 - 20,000 per month
Compensation
Comprehensive package
Experience
2 - 5 yrs
Seniority
Manager
Qualification
Bachelors degree
Expiration date
31/10/2025
Job description
As a member of the Microbiology Quality Control team, you will be responsible for conducting a range of microbiological tests to ensure compliance with regulatory and internal quality standards. Your key responsibilities will include testing sterile and non-sterile samples, microbiology assays, microbial culture testing, water testing, environmental monitoring, and lab support activities. You will manage compliance with GLP, GDP, and GMP, prepare and review SOPs, handle deviations through eQMS, and participate in audits. The role requires strong accountability, process compliance, organizational discipline, and proficiency in microbiology testing processes.
Required skills
Key responsibilities
- Perform testing of sterile samples including Sterility, LBPC (Limulus-Based Pyrogen Test), and BET (Bacterial Endotoxin Test) with proper documentation.
- Conduct testing of non-sterile samples, such as Microbial Limit Test (MLT) and Bioburden, along with accurate record-keeping.
- Perform microbiology assay testing and document results in compliance with GMP.
- Carry out microbiology culture testing including maintenance, sub-culturing, Growth Promotion Testing (GPT), and microbial identification.
- Perform water testing, release analysis, and related documentation.
- Conduct environmental monitoring in classified areas across Julphar production plants and microbiology labs, ensuring accurate and timely documentation.
- Execute various microbiology lab support activities including equipment monitoring, cleaning validations, and media preparation.
- Monitor equipment and area temperatures using Vaisala/SIRIUS systems.
- Ensure real-time documentation and compliance for all assigned tasks.
- Handle sample and result entries, reservation creation, and notification processes in SAP.
- Adhere strictly to Good Laboratory Practices (GLP), Data Integrity, and Good Documentation Practices (GDP).
- Prepare and review Standard Operating Procedures (SOPs) and support microbiology-related qualification/validation documentation.
- Participate in internal and external audits and promptly report any deviations, OOS (Out of Specification), OOL (Out of Limit), or excursions.
- Manage documentation and deviation handling through eQMS (Amplelogic system).
- Follow all safety protocols and ensure a clean and compliant laboratory environment.
- Ensure full compliance with company policies, GMP, and regulatory guidelines.
Experience & skills
- Bachelor’s or Master’s Degree in Microbiology or other Biological Sciences
- 4–6 years of relevant experience in a pharmaceutical microbiology lab (preferably in sterile and non-sterile product testing)
- Proficient in computer applications including MS Word, Excel, and PowerPoint
- Familiarity with SAP, eQMS (Amplelogic), and temperature monitoring systems like Vaisala/SIRIUS is a plus
