Finished Product Analyst – Quality Control Job Opening at Razi Al-Madinah Pharmaceuticals, Medina, Saudi Arabia

Apply now for the position of Finished Product Analyst – Quality Control at Razi Al-Madinah Pharmaceuticals in Medina, Saudi Arabia. Candidates with a degree in Pharmacy or Chemistry and a minimum of 2 years of QC experience in pharmaceuticals are encouraged to apply.

🚨 Job Opportunity in Saudi Arabia – Finished Product Analyst (Quality Control) at Razi Al-Madinah Pharmaceutical

Are you a skilled Quality Control professional with expertise in finished product testing? Are you seeking a prestigious career in the pharmaceutical industry in Saudi Arabia? Razi Al-Madinah Pharmaceutical, a leading pharmaceutical company in Medina, is urgently hiring for the position of Finished Product Analyst – Quality Control.

This is an exceptional opportunity for talented professionals who want to contribute to one of Saudi Arabia’s most respected pharma organizations and enjoy the benefits of working in a WHO-GMP-compliant environment with modern infrastructure and a supportive team culture.

📍 Job Location:

Razi Al-Madinah Pharmaceutical Industries
Medina, Saudi Arabia
(مدينة المنورة، المملكة العربية السعودية)

🎓 Job Requirements:

• Education:
  Bachelor’s degree in Pharmacy, Chemistry, or a related scientific discipline.

• Experience:
  Minimum 2 years of hands-on experience in pharmaceutical Quality Control, with a focus on finished product testing.

• Technical Knowledge:
  Familiarity with pharmacopeial standards such as USP, BP, and EP, along with GMP compliance and regulatory understanding.

🔬 Key Responsibilities:

As a Finished Product Analyst, you will be responsible for maintaining the highest standards of product quality and regulatory compliance. Your core duties will include: 

1. Analytical Testing:

   • Conduct routine and non-routine testing of finished pharmaceutical products to ensure they meet defined specifications.

   • Perform tests for assay, dissolution, disintegration, related substances, moisture content, etc.

2. Instrument Handling:

   • Proficient operation and maintenance of laboratory instruments such as:

     • HPLC (High-Performance Liquid Chromatography)

     • UV-Vis Spectrophotometer

     • FTIR (Fourier-Transform Infrared Spectroscopy)

     • Dissolution Testers, pH meters, and others.

   • Troubleshooting and calibration support.

3. Documentation & Reporting:

   • Preparation and review of analytical test reports, Certificates of Analysis (COAs), and lab documentation.

   • Compliance with Good Documentation Practices (GDP) and internal SOPs.

4. Deviation & OOS Handling:

   • Prompt reporting and assistance in the investigation of Out-of-Specification (OOS) or Out-of-Trend (OOT) results.

   • Collaborate with the QA team to ensure appropriate corrective actions.

5. Regulatory & Compliance:

   • Work in strict adherence to Good Laboratory Practices (GLP) and cGMP standards.

   • Maintain audit readiness and participate in internal and external audits.

6. Method Verification & Stability Testing:

   • Participate in analytical method validation/verification and stability testing programs.

   • Support the development of new methods and continuous improvement initiatives.

🧾 Desired Candidate Profile:

• Professional Attitude: Strong attention to detail, organizational skills, and commitment to quality.

• Communication: Clear and professional communication skills (written & verbal).

• Teamwork: Ability to work collaboratively with cross-functional teams including QA, production, and regulatory affairs.

• Readiness: Available to join immediately or within 30 days preferred.

💼 What’s in It for You?

✅ Competitive Salary (Commensurate with experience)

✅ Work in a WHO-GMP-certified pharmaceutical facility

✅ Exposure to advanced analytical instrumentation and global quality standards

✅ Opportunity for professional growth within a rapidly expanding company

✅ Friendly work culture based on integrity, teamwork, and innovation

✅ Be part of a company that supports career development and employee well-being

🏢 About Razi Al-Madinah Pharmaceutical

Razi Al-Madinah Pharmaceutical is a WHO-GMP and ISO 9001:2008 certified pharmaceutical company based in Medina, Saudi Arabia. Strategically located near Mysore Airport, the facility is designed as per the latest international GMP guidelines including EU-GMP and MHRA standards.

We specialize in the manufacturing of a wide range of therapeutic categories, ensuring affordability, efficacy, and safety of medications delivered to patients across regions.

At Razi, we take pride in our purpose-driven work culture and strive to maintain high standards in pharmaceutical manufacturing, compliance, and people development.

📤 How to Apply:

If this opportunity aligns with your career goals and professional background, we welcome you to submit your updated CV to the following email addresses:

📧 hr@razial-madina.com
📧 tm@razial-madina.com

For queries, you can also connect via WhatsApp or call the HR team.

📢 Important Note:

خير الناس أنفعهم للناس
“The best of people are those who are most beneficial to others.”

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