Leading pharmaceutical company based in Al Ain is seeking experienced QC Analyst professionals to join their quality control laboratory. This is an exceptional opportunity for a pharmaceutical analyst passionate about quality assurance. As QC Analyst, you’ll test raw materials, packaging, in-process samples, and finished products using HPLC, UV-Vis, Karl Fischer, and other instruments; conduct water system testing and microbiological sampling; perform daily lab operations and instrument checks; prepare analytical reports and Certificates of Analysis; support OOS/OOT investigations and regulatory compliance; and maintain GMP documentation and ALCOA+ records. Competitive benefits include life insurance, medical insurance, paid leaves, transportation, visa sponsorship, and travel allowance. 2 vacancies available for Filipino, Indian, or any nationality candidates.
About Our Pharmaceutical Company — Quality & Innovation Leader
Industry: Pharmaceutical, Biotech, and Clinical Research
Location: Al Ain, United Arab Emirates
Specialization: GMP pharmaceutical laboratory operations and quality control
Standards: BP/USP/EP pharmacopoeia compliance and regulatory adherence
Mission: Delivering pharmaceutical excellence through rigorous quality assurance
QC Analyst Role — Laboratory Testing & Quality Assurance
Department: Quality Control Laboratory
Primary Focus: Analytical testing, HPLC analysis, water system monitoring
Scope: Pharmaceutical product quality assurance across production
Mission: Ensuring pharmaceutical quality and regulatory compliance
QC Analyst Position Overview
The QC Analyst position at our pharmaceutical company represents a critical quality control role ensuring pharmaceutical excellence and regulatory compliance in Al Ain’s healthcare manufacturing. You’ll be responsible for comprehensive analytical testing across raw materials, packaging materials, in-process samples, and finished pharmaceutical products using state-of-the-art instrumentation. Your responsibilities include performing detailed analyses using HPLC (High-Performance Liquid Chromatography), UV-Vis spectroscopy, Karl Fischer titration, dissolution testing, disintegration testing, pH measurement, and other routine QC instruments against BP (British Pharmacopoeia), USP (United States Pharmacopoeia), EP (European Pharmacopoeia), and in-house specifications. You’ll conduct comprehensive stability studies and maintain detailed stability records, prepare and review analytical reports, generate Certificates of Analysis for clients, collect and test daily purified water samples from user points and distribution loops, test conductivity, TOC (Total Organic Carbon), pH and other chemical parameters per pharmacopoeia, collect microbiological samples and coordinate testing, track water results and trend data reporting excursions immediately, perform daily instrument checks including balance verification and HPLC system suitability, record and monitor laboratory temperature/humidity and equipment logs, receive/log/store samples and maintain retention samples, prepare and label reagents, volumetric solutions, and mobile phases, manage reference standards and chemical inventory with expiry control, maintain laboratory cleanliness and safe chemical waste disposal, support OOS (Out-of-Specification) and OOT (Out-of-Trend) investigations, assist with deviations and CAPA (Corrective and Preventive Action), support method validation and verification, participate in internal audits and PIC/S readiness activities, and maintain ALCOA+ (Attributable, Legible, Contemporary, Original, Accurate, plus complete audit trails) compliant records.
As QC Analyst, you’ll combine technical expertise with regulatory knowledge ensuring pharmaceutical products meet international quality standards, develop expertise in chromatography and spectroscopy techniques, support pharmaceutical production through rigorous quality assurance, maintain comprehensive laboratory documentation supporting compliance, collaborate with production teams ensuring quality standards, advance pharmaceutical career in GMP environment, and work within professional laboratory team supporting healthcare product quality. With 3-5 years GMP pharmaceutical laboratory experience, Bachelor’s degree in Chemistry or Pharmacy, hands-on HPLC experience, strong pharmacopoeia knowledge, excellent English communication, and availability to join within 4 weeks, this position offers excellent opportunity for pharmaceutical quality control professionals seeking roles in established GMP pharmaceutical operations.
Why This Role Matters: As QC Analyst at pharmaceutical company, you ensure pharmaceutical products are safe, effective, and compliant through rigorous quality testing, protect consumer health through analytical excellence, support pharmaceutical manufacturing through quality assurance, maintain regulatory compliance with international standards, advance pharmaceutical quality career with established company, work with advanced analytical instrumentation, contribute to healthcare product quality, and ensure GMP pharmaceutical excellence.
Key Responsibilities & QC Testing Duties
Testing & Analytical Analysis
- Test raw materials and packaging materials against BP/USP/EP specifications
- Analyze in-process samples and finished pharmaceutical products
- Perform analyses using HPLC and UV-Vis chromatography
- Conduct Karl Fischer titration and dissolution testing
- Execute disintegration testing and pH measurement
- Operate routine QC instruments with technical expertise
Stability Studies & Records Management
- Conduct comprehensive stability studies per protocols
- Maintain detailed stability study records and documentation
- Prepare and review analytical reports
- Generate Certificates of Analysis for pharmaceutical products
- Document testing procedures and results comprehensively
- Maintain ALCOA+ compliant records
Water System Testing & Monitoring
- Collect daily purified water samples from user points and distribution loop
- Test conductivity, TOC, pH, and chemical parameters
- Collect microbiological water samples
- Coordinate with microbiology testing team
- Track water results and trend analysis data
- Report excursions immediately to management
Daily Laboratory Operations
- Perform daily instrument checks and balance verification
- Conduct HPLC system suitability testing
- Record and monitor laboratory temperature and humidity
- Monitor fridge and incubator logs
- Receive, log, and store samples properly
- Maintain retention sample management
Reagent & Inventory Management
- Prepare and label reagents and volumetric solutions
- Prepare mobile phases for chromatography
- Manage reference standards and chemical inventory
- Control chemical expiry dates and rotation
- Maintain laboratory cleanliness and organization
- Ensure safe chemical waste disposal compliance
Quality Support & Regulatory Compliance
- Support OOS (Out-of-Specification) investigations
- Support OOT (Out-of-Trend) investigations
- Assist deviation and CAPA (Corrective Action) processes
- Support method validation and verification activities
- Prepare regulatory submission data
- Participate in internal audits and PIC/S readiness
Qualifications & Requirements
Educational Requirements
- Bachelor’s degree in Chemistry required
- Bachelor’s degree in Pharmacy acceptable
- Master’s degree in Chemistry preferred
Professional Experience
- 3-5 years QC experience in GMP pharmaceutical laboratory
- Hands-on HPLC experience with method running
- System suitability knowledge and troubleshooting
- Pharmaceutical product testing background
Technical Knowledge & Skills
- Strong knowledge of pharmacopoeia testing (BP/USP/EP)
- Expertise in HPLC operation and analysis
- UV-Vis spectroscopy knowledge
- Karl Fischer titration expertise
- GMP documentation and ALCOA+ compliance
- Laboratory instrument operation proficiency
Professional Competencies
- Good written and spoken English proficiency
- Strong analytical thinking and attention to detail
- Documentation and record-keeping accuracy
- Problem-solving and troubleshooting capability
- Ability to follow protocols and procedures
- Professional attitude and work reliability
Career Development & Growth Opportunities
Professional Advancement
- QC Analyst role with established pharmaceutical company
- Opportunity to advance to Senior QC Analyst positions
- Career growth in pharmaceutical quality field
- Exposure to regulatory and compliance advancements
Benefits & Compensation
- Competitive salary: AED 2,500-3,500 per month
- Life Insurance coverage
- Medical Insurance benefits
- Paid leave entitlements
- Transportation allowance
- Visa sponsorship provided
- Travel allowance support
About Our Pharmaceutical Company — Healthcare Excellence Leader
Our pharmaceutical company represents a quality-focused healthcare manufacturer committed to producing safe, effective, and compliant pharmaceutical products. Based in Al Ain’s pharmaceutical hub, the company operates world-class GMP laboratory facilities maintaining highest quality standards. The organization specializes in pharmaceutical product development, manufacturing, and quality assurance supporting healthcare needs across the UAE and regional markets. The company values quality professionals dedicated to pharmaceutical excellence, rigorous analytical standards, and regulatory compliance ensuring patient safety.
Career Excellence in Pharmaceutical QC: Join established pharmaceutical company, perform rigorous quality testing ensuring pharmaceutical excellence, work with advanced HPLC and analytical instrumentation, develop expertise in pharmacopoeia standards and GMP compliance, support pharmaceutical manufacturing through quality assurance, advance pharmaceutical career with healthcare leader, work in professional laboratory environment, contribute to pharmaceutical safety and efficacy, and enjoy competitive compensation with comprehensive benefits.
Who Should Apply?
- Pharmaceutical Analysts: With GMP laboratory experience
- QC Professionals: From pharmaceutical backgrounds
- Chemistry Graduates: With 3-5 years experience
- Laboratory Technicians: Ready for analyst roles
- HPLC Specialists: Seeking pharmaceutical positions
- International Candidates: From any nationality (Filipino, Indian preferred)
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