Quality Control Section Head

Eva Pharma; Saudi Arabia; On-site; SAR 150,000 - 200,000; Full time

Job summary

A leading pharmaceutical company in Saudi Arabia is seeking a Quality Control Section Head to join their team. The ideal candidate will have a Bachelor’s degree in pharmacy or a related field, with 8-10 years of experience in pharmaceutical manufacturing and a strong knowledge of GMP documentation. This role involves leading QC laboratory setup, ensuring compliance with various regulatory guidelines, and preparing for audits.

Qualifications

• 8–10 years in pharmaceutical manufacturing
• Saudi experience is a must
• Experience in handling injectables and oral solids

Responsibilities

• Lead the setting up of QC laboratories and execute qualification and calibration of QC instruments.
• Ensure adherence to cGMP, SFDA, ICH, FDA, EMA guidelines.
• Prepare for and participate in internal and external audits.

Skills

Analytical techniques (HPLC, GC, UV, IR)

GMP documentation

Regulatory audits

Education

Bachelor’s degree in pharmacy, Chemistry, or Life Sciences

Job description

Overview

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 “Quality Control Section Head” to join our dynamic team in Sudair City - 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 the setting up of QC laboratories and Plan, coordinate, and execute qualification and calibration of QC instruments, as well as Develop laboratory readiness plan to support site commissioning and validation
• Ensure timely and accurate execution of stability studies and method validations, as well as Review and approve analytical data and reports.
• Ensure adherence to cGMP, SFDA, ICH, FDA, EMA, and other applicable regulatory guidelines.
• Maintain and approve SOPs, STPs, specifications, and other QC documentation and Lead investigations for OOS, deviations, and complaints, ensuring CAPA implementation.
• Prepare for and participate in internal and external audits and ensure timely closure of audit observations and CAPAs.

Qualifications

• Bachelor’s degree in pharmacy, Chemistry, or Life Sciences.
• 8–10 years in pharmaceutical manufacturing
• Saudi Experience is a Must
• Experience in handling injectables, oral solids, and regulatory audits.
• Strong knowledge of analytical techniques (HPLC, GC, UV, IR).
• Proficient in GMP documentation and data integrity principles.