Biotechnology Industry – Quality Control Analyst

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Full-time

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Opportunities for a QC Analyst to join a quality control laboratory in Jeddah, Saudi Arabia, for a leading Biotechnology Industry. In this role, you will perform analytical testing, work closely with laboratory colleagues, technical teams, and quality partners, and ensure the delivery of reliable and accurate test results.

Job Responsibilities

As a QC Analyst, you will take ownership of critical laboratory activities and play a key role in ensuring product quality and compliance. Your responsibilities will include:

  • Analytical Testing: Perform routine chemical and microbiological testing of raw materials, in-process samples, and finished products using approved methods and laboratory instruments.
  • Laboratory Documentation: Prepare reagents, maintain laboratory records, and complete test documentation accurately in compliance with standard procedures.
  • Compliance & Quality: Follow and uphold data integrity principles, quality management practices, and Good Manufacturing Practices (GMP) requirements.
  • Equipment Maintenance: Carry out equipment checks, assist with basic maintenance, and participate in calibration and validation activities.
  • Investigations: Support investigations into out-of-specification (OOS) results and document findings clearly for review.
  • Team Support & Training: Assist in training new laboratory analysts, sharing practical knowledge, and fostering a collaborative environment to ensure accurate and timely test results.

Job Qualifications

  • Bachelor’s degree in Chemistry, Biochemistry, Pharmacy, Microbiology, or a related scientific discipline.
  • Minimum 2 years of experience in a laboratory setting, preferably in QC or analytical testing.
  • Working knowledge of GMP, GLP, and laboratory safety (EHS) standards.
  • Practical experience with common laboratory instruments and analytical techniques.
  • Strong written and verbal English communication skills for documentation and teamwork.
  • Proficiency in basic computer tools such as Microsoft Word and Excel.
  • Experience in stability testing, method transfer, or validation activities.
  • Familiarity with quality management systems and risk-based laboratory practices.
  • Ability to troubleshoot and maintain laboratory instruments.
  • Exposure to both microbiological and chemical testing.
  • Training or experience in data integrity practices and record keeping.
  • Strong problem-solving, organizational, and time management skills.

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