A reputable pharmaceutical company in Ras Al Khaimah, UAE is hiring a skilled and detail-oriented QC Specialist (Jr. Specialist – QC) to perform chemical and physical analysis of raw materials, semi-finished products, and stability samples in full compliance with approved specifications, SOPs, GMP, and GLP standards. This is an excellent career opportunity for a qualified pharmaceutical analyst with 3–6 years of hands-on HPLC, GC, dissolution, and UV-Vis experience, strong knowledge of USP, EP, and BP pharmacopoeial standards, and proficiency in SAP and AmpleLogic systems — in one of the UAE’s most stable pharmaceutical manufacturing environments.
About the Role — QC Specialist Pharmaceutical RAK UAE
Industry: Pharmaceutical manufacturing — quality control laboratory operations in Ras Al Khaimah, UAE
Analytical Scope: Raw materials, semi-finished products, and stability samples testing per approved methods and pharmacopoeial standards
Regulatory Framework: GMP, GLP, GDP, ALCOA+, USP, EP, BP, and applicable UAE regulatory requirements
Systems Used: SAP for data entry and AmpleLogic for QMS activities including CAPA, AMS, and Change Controls
Collaboration: Cross-functional coordination with Quality Assurance, Production, and R&D departments
Pharmaceutical QC Career Opportunity in RAK UAE
Stable Industry: Pharmaceutical manufacturing in Ras Al Khaimah is a growing, well-regulated, and career-stable sector in the UAE
Technical Growth: Build deep analytical expertise in HPLC, GC, dissolution, method validation, and regulatory compliance
Career Advancement: Clear pathway to Senior QC Analyst, QC Supervisor, QA Manager, and Validation Specialist roles in the UAE pharma industry
Professional Environment: Structured SOPs, GMP compliance culture, and continuous improvement focus — ideal for analytically driven professionals
Position Overview
The QC Specialist (Jr. Specialist – QC) at this pharmaceutical facility in Ras Al Khaimah is a full-time, on-site analytical laboratory role responsible for performing chemical and physical analysis of raw materials, semi-finished products, and stability samples in full compliance with approved analytical methods, pharmacopoeial standards, GMP, GLP, and company SOPs. You will operate advanced QC instruments including HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus; maintain accurate laboratory records in SAP; support QMS activities through AmpleLogic; participate in internal and external audits; and contribute to continuous improvement of laboratory efficiency, data integrity, and regulatory compliance across the quality control function.
Why This Role Matters: As QC Specialist in Ras Al Khaimah’s pharmaceutical sector, you will be a critical guardian of product quality and patient safety — ensuring every raw material, semi-finished product, and stability sample meets the highest pharmacopoeial and regulatory standards before reaching patients, build advanced analytical expertise in HPLC, GC, and dissolution testing within a fully GMP-compliant professional environment, and develop a meaningful pharmaceutical QC career at a structured, compliance-driven organization in one of the UAE’s most active pharmaceutical manufacturing hubs.
Key Responsibilities
Analytical Testing & Laboratory Operations
- Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples in strict accordance with approved analytical methods, specifications, and SOPs
- Operate QC laboratory equipment including HPLC, GC, UV-Vis spectrophotometers, dissolution apparatus, and other applicable analytical instruments safely and accurately
- Ensure all analytical testing activities are performed accurately and within established timelines — in full compliance with GMP, GLP, and applicable regulatory requirements
- Ensure tested products meet established quality specifications and applicable pharmacopoeial standards including USP, EP, and BP throughout all testing activities
- Assist in troubleshooting analytical issues and resolving day-to-day laboratory operational challenges — escalating unresolved issues to QC supervisors as appropriate
Data Integrity, Documentation & SAP Management
- Maintain accurate and complete records of analytical results, laboratory observations, and testing activities in accordance with Good Documentation Practices (GDP) at all times
- Enter analytical results and all relevant laboratory data into SAP accurately and within established timeframes — ensuring complete and auditable data trails
- Ensure full compliance with data integrity principles and ALCOA+ requirements across all laboratory activities — protecting the accuracy, completeness, and traceability of all QC data
- Maintain laboratory cleanliness, hygienic working conditions, and proper handling of all laboratory materials, chemicals, and equipment in compliance with EHS standards
Quality Management System & Audit Support
- Handle and support Quality Management System (QMS) activities including CAPA, AMS, and Change Controls through the AmpleLogic system — ensuring timely and compliant closure
- Support analytical method validation and method transfer activities as required — following approved validation protocols and regulatory requirements
- Participate in internal and external regulatory audits — providing required laboratory documentation, sample data, and analytical records to support timely and favorable audit outcomes
- Coordinate effectively with Quality Assurance, Production, R&D, and other departments to support quality and operational requirements across the pharmaceutical facility
EHS, Safety & Continuous Improvement
- Use appropriate Personal Protective Equipment (PPE) and follow all safe laboratory practices to minimize workplace hazards and operational risks throughout every working shift
- Ensure daily laboratory operations comply with Environmental Management System (EMS) and Environmental, Health, and Safety (EHS) standards applicable to the facility
- Identify, report, and actively support the prevention of environmental impacts and safety risks associated with all laboratory activities and chemical handling
- Contribute actively to continuous improvement initiatives aimed at enhancing laboratory efficiency, analytical accuracy, quality compliance, and overall operational performance
Qualifications & Requirements
Educational Background
- Bachelor’s degree in Pharmacy, Chemistry, or a related Science discipline is required for this pharmaceutical QC Specialist role in Ras Al Khaimah, UAE
- Additional professional development or certifications in analytical chemistry, method validation, or pharmaceutical quality systems are a strong advantage
Experience Requirements
- Minimum 3 to 6 years of relevant experience in pharmaceutical Quality Control — with proven hands-on expertise in HPLC, GC, UV-Vis, dissolution, and analytical troubleshooting
- Sound practical knowledge of GMP, GLP, SOPs, and applicable regulatory guidelines including USP, EP, and BP pharmacopoeial standards
- Experience in analytical method validation, method transfer, and assay analysis within a GMP-compliant pharmaceutical manufacturing environment
- Strong understanding of data integrity principles, ALCOA+ compliance, and Good Documentation Practices in a regulated laboratory setting
- Working knowledge of QMS activities including CAPA, AMS, Change Controls, and audit compliance — ideally with experience in AmpleLogic or similar QMS platforms
- Proficiency in SAP for laboratory data entry and result documentation, alongside general computer software applications
About the Pharmaceutical QC Opportunity — Ras Al Khaimah UAE
Ras Al Khaimah has established itself as one of the UAE’s most important pharmaceutical manufacturing hubs, with a growing cluster of GMP-certified facilities producing a wide range of pharmaceutical products for domestic and international markets. Companies operating in RAK’s pharmaceutical sector benefit from a well-developed regulatory environment, strong government support for manufacturing investment, and a skilled workforce of pharmaceutical professionals drawn from across the UAE and the broader GCC region. For QC specialists, Ras Al Khaimah offers excellent career stability, competitive compensation, and a professional, compliance-focused work environment that supports genuine long-term career growth in the pharmaceutical analytical sciences.
Career Path: A QC Specialist role in Ras Al Khaimah’s pharmaceutical sector provides a strong foundation for advancement toward Senior QC Analyst, QC Supervisor, QA Specialist, Validation Scientist, and Regulatory Affairs Officer positions — all high-demand and well-compensated roles across the UAE and GCC pharmaceutical industry.
Who Should Apply?
- Pharmaceutical QC Analysts: With 3–6 years of hands-on HPLC, GC, dissolution, and UV-Vis experience in a GMP-compliant UAE or GCC pharma facility
- Pharmacy / Chemistry Graduates: With solid analytical testing experience and strong knowledge of USP, EP, BP, and ALCOA+ data integrity requirements
- SAP & AmpleLogic Users: With proficiency in pharmaceutical QMS platforms for CAPA, AMS, and Change Control management in a regulated environment
- Method Validation Specialists: With proven experience in analytical method validation, method transfer, and assay analysis for pharmaceutical products
- UAE-Based QC Professionals: Ready to contribute to a structured, compliance-driven pharmaceutical QC laboratory in Ras Al Khaimah with minimal transition time
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