Quality Control Specialist

TALENTMATE; Ras Al Khaimah; On-site; AED 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical manufacturer in Ras Al Khaimah is seeking a Quality Control Specialist responsible for ensuring compliance with cGMP guidelines, conducting chemical and physical analysis of products, and operating various QC equipment. The ideal candidate should hold a Bachelor's degree in Pharmacy or Science and have at least 2 years of relevant experience. This entry-level full-time role offers opportunities for training and development in a supportive environment that values diversity and professionalism.

Qualifications

• Minimum 2 years’ experience in the same field.
• Proficient with computer software applications.
• Experience adhering to cGMP principles.

Responsibilities

• Carry out chemical and physical analysis of products.
• Operate various QC equipment as required.
• Train newly joined staff on applicable procedures.

Skills

Attention to detail

Communication skills

Problem-solving skills

Accountability

Interpersonal skills

Education

Bachelor’s degree in Pharmacy or Science

Tools

SAP

HPLC

GC

Job description

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.

Our core values: Respect, Collaboration, Innovation, Integrity and Compassion, combined with a focus on diversity, inclusion and equal opportunities, are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable talent, create a healthy work environment and accomplish our goals through world‑class research and with the compassion and commitment of our employees.

Job Summary / Main Purpose

The Specialist in the Quality Control division at Julphar HQ – RAK is responsible for adhering to cGMP principles and maintaining them effectively. The role involves carrying out chemical and physical analysis of finished products, raw materials, and stability samples, as well as process validation. The Specialist operates various QC equipment, follows GLP, GMP and safety procedures, and maintains hygienic conditions in the lab. Additionally, the Specialist is responsible for entering data on SAP, recording all working data, assisting supervisors, training newly joined staff, and ensuring final products adhere to all specifications and regulations. The role also includes creating and processing HPLC & GC analytical methods, performing investigations for lab incidents, and supporting external and internal audits.

Key Responsibilities

• Adhere to and maintain cGMP principles effectively.
• Carry out chemical and physical analysis of finished products, raw materials, and stability samples, and support process validation.
• Operate various QC equipment as required.
• Follow GLP, GMP and safety procedures and maintain hygienic lab conditions.
• Enter and record all working data on SAP.
• Support supervisors in assigned tasks.
• Train newly joined staff and QA personnel on applicable procedures.
• Assist in troubleshooting and solving day‑to‑day operational problems.
• Ensure final products meet all specifications and regulations.
• Create HPLC & GC analytical methods from approved STM/Pharmacopeia before starting analysis.
• Process and approve all HPLC & GC analytical data and review audit trails for instruments.
• Train QC personnel and qualify analysts to perform QC analyses.
• Ensure analyses are performed correctly as per applicable procedures.
• Investigate lab incidents, OOS/OOT results, deviations and implement corrective and preventive actions.
• Lock results in SAP and create notifications for consumable stock management.
• Support and close external and internal audit observations.
• Review and approve protocols and reports such as method validation, method transfer, process validation and stability.
• Handle and close quality management system actions like Deviations, OOS, CAPAs, AMS and change controls using the Amplelogic system.
• Ensure data integrity and good documentation practices in the QC labs.
• Perform additional tasks assigned by the Head of the department or designee.

Core Competency

• Highly oriented with strong accountability & ownership.
• High process compliance and implementation skills with strong attention to detail.
• Strong communication, interpersonal and problem‑solving skills.
• Business acumen combined with a dedication to legality.
• Able to manage tasks and priorities and adapt to changing situations.
• Highly disciplined, organized, self‑motivated to learn and implement new knowledge.
• Capable of working cross‑functionally with internal and external departments.

Qualifications, Key Experiences / Functional Knowledge Requirements

• Bachelor’s degree in Pharmacy or Science.
• Minimum 2 years’ experience in the same field.
• Proficient with computer software applications.
• Experience adhering to cGMP principles and maintaining effective practices.
• Proficiency in conducting chemical and physical analysis for RM, FP and stability.
• Experience operating various QC equipment and ensuring compliance with GLP, GMP and safety procedures.

We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar.

Job Details: Role Level – Entry‑Level | Work Type – Full‑Time | Country – United Arab Emirates | City – Ras Al Khaimah | Company Website – www.julphar.net | Job Function – Quality Assurance & Control | Industry – Pharmaceutical Manufacturing.