Microbiology Section Head

Eva Pharma; Saudi Arabia; On-site; SAR 300,000 - 400,000; Full time

Job summary

A leading pharmaceutical company in Saudi Arabia is seeking a Microbiology Section Head to lead and manage a microbiology team. The ideal candidate should have extensive experience in microbiology and a solid understanding of GMP and regulatory compliance. Responsibilities include overseeing microbiological testing and ensuring laboratory readiness for audits. This role offers a chance to contribute to health and well-being initiatives and work in a supportive environment.

Qualifications

• Experience in microbiology, especially in sterile and non-sterile product environments.
• Strong understanding of GMP and regulatory requirements.
• Proven leadership and team management skills.

Responsibilities

• Lead and mentor the microbiology team.
• Ensure compliance with GMP and regulatory standards.
• Oversee microbiological testing activities.

Job description

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary

We are seeking a passionate and talented “Microbiology Section Head” to join our dynamic team in Sudair - Saudi Arabia. Theideal candidate will contribute to our mission of enhancing human health and well-being,ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities

• Lead, manage, and mentor the microbiology team responsible for both sterile and non-sterile products.
• Foster a collaborative and high-performance culture within the team, ensuring adherence to GMP, regulatory requirements, and internal quality standards.
• Oversee all microbiological testing activities, including sterility testing, microbial limit testing, bioburden analysis, endotoxin testing, and environmental monitoring.
• Prepare for and support internal and external audits, ensuring laboratory operations are always audit-ready.
• Ensure that validated methods are transferred effectively to the production environment and maintained in compliance with regulatory requirements.