Quality Control Analyst
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Key skills for this role
About the Role
Pharma Pharmaceutical Industries seeks a Quality Control Analyst to perform laboratory testing of raw materials, in-process samples, and finished products in Riyadh. Requires 2-6 years of experience in pharmaceutical analytical R&D or QC with expertise in HPLC, UV-Vis, FT-IR, and dissolution testing.
Key Skills for This Role
Responsibilities
- Perform routine and non routine laboratory testing of raw materials, in process samples, and finished pharmaceutical and biological products
- Prepare samples, operate and maintain laboratory equipment, document test results, and interpret data in accordance with internal procedures and regulatory guidelines
- Collaborate with Quality Assurance and Production teams to investigate deviations, support root cause analysis, and implement corrective actions
- Maintain accurate records, adhere to safety and GMP requirements, and participate in continuous improvement initiatives for laboratory processes
Requirements
- Strong expertise in HPLC systems equipped with UV, PDA, and RI detectors, including method development, validation, and troubleshooting
- Proficiency in UV Visible spectroscopy for assay and dissolution analysis
- Experience with FT IR spectroscopy for raw material characterization
- Hands on experience in dissolution testing, including comparative dissolution profile studies
- Familiarity with chromatography data systems such as Empower and LabSolutions
- Proven experience in analytical method development, validation, and method transfer activities
- Relevant industry experience of 2–6 years in pharmaceutical analytical R&D or QC
- Preference will be given to Saudi nationals; non Saudi candidates must hold a valid IQAMA
- Candidates should be available to join within a short notice period (preferably within 2 weeks)
Full Job Posting
Company Description
- Pharma Pharmaceutical Industries & Biological Products (PPI) is a specialized provider of pharmaceutical and biological solutions for patients and healthcare professionals in Saudi Arabia, the GCC, and global markets.
Role Description
- The Quality Control Analyst is a full time, on site role based in Riyadh. The person in this role performs routine and non routine laboratory testing of raw materials, in process samples, and finished pharmaceutical and biological products to ensure they meet established quality standards.
Daily Responsibilities
- Preparing samples, operating and maintaining laboratory equipment, documenting test results, and interpreting data in accordance with internal procedures and regulatory guidelines.
- Collaborating with Quality Assurance and Production teams to investigate deviations, support root cause analysis, and implement corrective actions.
- Maintaining accurate records, adhering to safety and GMP requirements, and participating in continuous improvement initiatives for laboratory processes.
Eligibility Criteria
- Strong expertise in HPLC systems equipped with UV, PDA, and RI detectors, including method development, validation, and troubleshooting
- Proficiency in UV Visible spectroscopy for assay and dissolution analysis
- Experience with FT IR spectroscopy for raw material characterization
- Hands on experience in dissolution testing, including comparative dissolution profile studies
- Familiarity with chromatography data systems such as Empower and LabSolutions
- Proven experience in analytical method development, validation, and method transfer activities
- Relevant industry experience of 2–6 years in pharmaceutical analytical R&D or QC
- Preference will be given to Saudi nationals; non Saudi candidates must hold a valid IQAMA
- Candidates should be available to join within a short notice period (preferably within 2 weeks)
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