Specialist - Quality Control
Client of Talentmate
Employer Active
Posted 19 hrs ago
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Experience
6 - 8 Years
Job Location
Education
Bachelor of Business Administration(Management)
Nationality
Any Nationality
Gender
Not Mentioned
Vacancy
1 Vacancy
Job Description
Roles & Responsibilities
At Julphar, we are on a journey of culture transformation & 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.
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:
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.
- 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.
- 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)
- 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
Company Industry
- Recruitment
- Placement Firm
- Executive Search
Department / Functional Area
- Installation
- Maintenance
- Operations
- Repair
Keywords
- Specialist - Quality Control
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