Specialist - Quality Control

Overview

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Specialist - Quality Control

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Julphar . Get AI-powered advice on this job and more exclusive features. At Julphar, we are on a journey of culture transformation and our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism. Our core values : Respect, Collaboration, Innovation, Integrity and Compassion - combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents, create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

Responsibilities

Microbiological Testing & Analysis

– 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.

Water & Environmental Testing

– 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.

Lab Support Activities

– 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.

Compliance & Documentation

– 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).

Safety & Best Practices

– Follow all safety protocols and ensure a clean and compliant laboratory environment.

Ensure full compliance with company policies, GMP, and regulatory guidelines.

Core Competencies

– Strong sense of accountability and ownership; Highly disciplined, motivated, and well-organized; Excellent process compliance and implementation skills; Effective time and task management; Proficient English communication skills (verbal and written).

Qualifications & Functional Knowledge

– 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.

We value people from different backgrounds. Could this be your story? Apply today or visit to read more about us and the journey of Julphar

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing

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