A pharmaceutical manufacturing company in Ras Al Khaimah is hiring a Jr. Specialist – QC to perform chemical and physical analysis of raw materials, semi-finished products, and stability samples in accordance with approved specifications, SOPs, GMP, and GLP, while maintaining laboratory documentation, data integrity, and supporting quality management system activities across the QC laboratory.
About This Quality Control Opportunity
Sector Focus: Pharmaceutical Quality Control laboratory operations
Standards Scope: GMP, GLP, USP, EP, and BP pharmacopoeial compliance
Systems Used: SAP and AmpleLogic for laboratory data and QMS activities
Location: Ras Al Khaimah — a growing pharmaceutical manufacturing hub in the UAE
Career Impact & Growth Opportunity
Hands-On Analytical Work: Operate HPLC, GC, UV-Vis, dissolution apparatus, and other analytical instruments
Regulatory Exposure: Build expertise in GMP, GLP, data integrity (ALCOA+), and Good Documentation Practices
QMS Involvement: Support CAPA, AMS, and Change Control activities through the AmpleLogic system
Career Growth: Build a specialised pharmaceutical QC career with exposure to audits and method validation
Position Overview
This Jr. Specialist – QC role performs chemical and physical analysis of raw materials, semi-finished products, and stability samples in accordance with approved analytical methods, specifications, and SOPs. You will operate QC laboratory equipment including HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus, ensure compliance with GMP, GLP, and regulatory requirements, maintain accurate laboratory documentation, and support quality management system activities including CAPA, AMS, and Change Controls.
Why This Role Matters: As Jr. Specialist – QC, you play a direct role in ensuring pharmaceutical products meet USP, EP, and BP quality standards before reaching patients, gain hands-on experience with HPLC, GC, and other advanced analytical instruments, build expertise in data integrity, ALCOA+, and Good Documentation Practices essential across the pharma industry, contribute to method validation, audits, and continuous improvement initiatives, and grow your career within a structured, GMP-compliant Quality Control laboratory environment.
Key Responsibilities
Analytical Testing & Instrument Operation
- Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples
- Operate QC laboratory equipment including HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus
- Ensure analytical testing is performed accurately and within established timelines
- Ensure tested products meet quality specifications and pharmacopoeial standards (USP, EP, BP)
Documentation, Data Integrity & Compliance
- Maintain accurate and complete records in accordance with Good Documentation Practices (GDP)
- Enter analytical results and laboratory data into SAP accurately and on time
- Ensure compliance with data integrity principles and ALCOA+ requirements
- Support analytical method validation and method transfer activities
QMS, Audits & EHS Support
- Handle QMS activities including CAPA, AMS, and Change Controls through the AmpleLogic system
- Participate in internal and external audits and support timely closure of observations
- Follow SOPs, laboratory safety procedures, and company quality policies
- Ensure daily operations comply with EMS and EHS standards, using appropriate PPE
- Coordinate with QA, Production, R&D, and other departments to support quality requirements
Qualifications & Requirements
Educational Requirements
- Bachelor’s degree in Pharmacy, Chemistry, or a related Science discipline
Experience Requirements
- Minimum 3–6 years of relevant experience in pharmaceutical Quality Control
- Hands-on experience in HPLC, GC, UV-Vis spectrophotometry, dissolution testing, and other analytical techniques
- Experience in analytical method validation, method transfer, and assay analysis
Essential Skills
- Sound knowledge of GMP, GLP, SOPs, and regulatory guidelines including USP, EP, and BP
- Strong understanding of data integrity principles, ALCOA+ compliance, and GDP
- Working knowledge of QMS activities including CAPA, AMS, Change Controls, and audit compliance
- Proficiency in SAP, AmpleLogic, and other computer software applications
- Strong analytical, troubleshooting, and problem-solving skills with excellent attention to detail
- Effective communication skills and ability to work collaboratively across cross-functional teams
About This Pharmaceutical Manufacturing Opportunity
This role sits within a pharmaceutical Quality Control laboratory based in Ras Al Khaimah, UAE, responsible for ensuring raw materials, semi-finished products, and stability samples consistently meet approved specifications, GMP, and GLP standards. The QC laboratory plays a critical role in safeguarding product quality and regulatory compliance across the pharmaceutical manufacturing process, from raw material testing through to final product release.
Career Excellence: Build a specialised pharmaceutical QC career in one of the UAE’s growing manufacturing hubs.
Who Should Apply?
- Pharmacy & Chemistry Graduates: With 3-6 years of pharmaceutical QC experience
- Analytical Chemists: Skilled in HPLC, GC, UV-Vis, and dissolution testing
- GMP/GLP Compliance Specialists: Familiar with USP, EP, and BP pharmacopoeial standards
- Data Integrity & Documentation Professionals: Experienced with ALCOA+ and GDP requirements
- QMS-Trained Candidates: Comfortable with CAPA, AMS, Change Controls, and audit support
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