Specialist QC Jobs Ras Al Khaimah UAE 2026

A pharmaceutical manufacturer in Ras Al Khaimah, UAE is hiring a Specialist — Quality Control (QC) to perform chemical and physical analysis of raw materials, semi-finished products, and stability samples under approved specifications, SOPs, GMP, and GLP. You will operate HPLC, GC, UV-Vis, and dissolution equipment, keep accurate lab records, protect data integrity (ALCOA+), enter results in SAP, and support CAPA, AMS, and change controls through AmpleLogic. The role needs a Bachelor’s degree in Pharmacy, Chemistry, or a related science and 3–6 years of pharmaceutical QC experience.

About the Role & Employer — Ras Al Khaimah Pharma

Environment: A regulated pharmaceutical manufacturing site with a dedicated QC laboratory

Location: Ras Al Khaimah — a growing industrial and pharmaceutical hub in the northern emirates

Teams: You will work with Quality Assurance, Production, R&D, and QC supervisors

Confidential Search: The company name is shared with shortlisted candidates during recruitment

What Your Day in the QC Lab Looks Like

Testing: Chemical and physical analysis against approved methods and specifications

Instruments: HPLC, GC, UV-Vis spectrophotometers, dissolution apparatus, and other analytical tools

Standards: Results must meet USP, EP, and BP pharmacopoeial requirements

Systems: SAP for results and AmpleLogic for CAPA, AMS, and change controls

Safety: EMS and EHS standards, PPE, and safe lab practice in every task

Why This QC Specialist Role in Ras Al Khaimah Stands Out: This is a real bench role with real responsibility. You run the instruments, protect the data, and support method validation, transfers, and audits — all in a regulated environment that values accuracy. For a pharmaceutical QC analyst with a few years of experience, it is a clear step up toward senior laboratory positions in the UAE’s growing pharma sector.

As Specialist — QC in Ras Al Khaimah, you will test raw materials, semi-finished products, and stability samples to approved methods, specifications, and SOPs, within set timelines. You will operate HPLC, GC, UV-Vis, and dissolution equipment, make sure products meet USP, EP, and BP standards, and keep complete records under Good Documentation Practices. You will enter results into SAP, follow ALCOA+ data integrity principles, support method validation and transfer, and handle CAPA, AMS, and change controls in AmpleLogic. You will also join internal and external audits, troubleshoot lab issues, follow EMS and EHS rules, and work with QA, Production, and R&D.

Key Responsibilities

• Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples using approved methods, specifications, and SOPs.
• Operate QC equipment, including HPLC, GC, UV-Vis spectrophotometers, dissolution apparatus, and other analytical instruments.
• Finish testing accurately and on time, in line with GMP, GLP, and regulatory requirements.
• Make sure tested products meet specifications and pharmacopoeial standards, including USP, EP, and BP.

• Keep accurate, complete records of results, laboratory observations, and testing activity under Good Documentation Practices.
• Enter results and lab data into SAP accurately and on time.
• Follow data integrity principles and ALCOA+ requirements in every lab activity.

• Support analytical method validation and method transfer as needed.
• Handle QMS activities — CAPA, AMS, and change controls — through the AmpleLogic system.
• Join internal and external audits, provide lab documents, and help close audit observations on time.

Safety, Environment & Lab Housekeeping

• Follow approved SOPs, lab safety procedures, and company quality policies strictly.
• Keep the lab clean and hygienic, and handle materials and equipment properly.
• Meet EMS and EHS standards daily, wear the right PPE, and report and help prevent environmental and safety risks.
• Take part in EHS activities, audits, and continual improvement work.

Collaboration & Continuous Improvement

• Troubleshoot analytical issues and help solve day-to-day lab challenges.
• Work with Quality Assurance, Production, R&D, and other departments, and support QC supervisors in assigned tasks.
• Contribute to improvement initiatives that raise lab efficiency, analytical accuracy, compliance, and performance.

Qualifications & Experience

Bachelor’s degree in Pharmacy, Chemistry, or a related science discipline.

Minimum 3–6 years of relevant experience in pharmaceutical Quality Control.

Hands-on experience with HPLC, GC, UV-Vis, dissolution testing, and other pharmaceutical analytical techniques.

Sound knowledge of GMP, GLP, SOPs, and guidelines including USP, EP, and BP.

 Who Should Apply?

• Pharma QC Analysts in the UAE: Professionals with 3–6 years of hands-on testing who want a specialist-level role in Ras Al Khaimah.
• HPLC & GC Experts: Analysts with strong chromatography and dissolution experience and a good record of accurate results.
• Data Integrity-Minded Chemists: People who follow ALCOA+ and Good Documentation Practices without shortcuts.
• QMS-Experienced Lab Staff: Candidates who have handled CAPA, change controls, and audit observations, ideally in AmpleLogic or similar systems.
• Pharmacy & Chemistry Graduates Ready to Grow: Bachelor’s holders with solid QC experience who are eager to learn new techniques and take ownership.

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