Specialist - QC

Julphar; Ras Al Khaimah; On-site; AED 89,000 - 156,000; Full time

Job summary

Julphar in Ras Al Khaimah is seeking a QC Analyst to ensure GLP, GMP and safety compliance in the laboratory. You will perform chemical and physical analyses of finished products and raw materials, operate QC instruments, and record data in SAP.

The ideal candidate holds a Bachelor's degree in pharmacy or science and 3–6 years of relevant experience, with strong data integrity, communication, and problem-solving skills.

Qualifications

• Bachelor's degree in pharmacy/science.
• Minimum 3-6 years' experience in the same field.
• Proficient with computer software application.

Responsibilities

• Ensure and follow GLP, GMP, safety procedures and maintain hygienic lab conditions.
• Carry-out chemical and physical analyses of finished/raw material/stability samples.
• Operate QC equipment per section requirements.
• Record all analytical data accurately and enter data into SAP.
• Ensure final products meet specifications and regulations.
• Support external and internal audits and close audit observations on time.
• Follow SOPs strictly and assist in troubleshooting daily operations.

Skills

Strong communication

Problem-solving

Data integrity

Documentation

Computer literacy

Education

Bachelor's degree in pharmacy/science

Tools

HPLC

GC

UV-Vis spectrophotometry

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 Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

Detailed Job Description

• To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.
• Responsible to carry-out chemical and physical analysis of Simi Finished /Raw Material / Stability.
• Responsible for the operation of various QC equipment (depending on the section he is working)
• Responsible for recording all working data
• Entering data of analysis on SAP
• Ensure Final Products adhere to all specifications and regulations.
• To ensure the analysis is performed correctly as per applicable procedures
• To involve and support external and internal audits and to close the audit observations on time.
• Responsible for handling of Quality management system actions like CAPAs, AMS and Change controls using Ample logic system.
• To follow and ensure data integrity and good documentation practices are implemented in the QC labs.
• To follow Standard Operating Procedures (SOPs) strictly
• Assist in trouble shooting and solving problems that may come up in the day-to-day operation of the department.
• Helps supervisors/Designate in assigned tasks.

Core Competency

• Highly oriented with strong sense of accountability & ownership.
• Has Strong communication, interpersonal and problem-solving skills.
• Business acumen partnered with a dedication to legality.
• Must be able to manage tasks and priorities and easily adapt to changing situations.
• Highly disciplined and must be organized, self-motivated to learn new learnings and implement them at workplace.
• Proficient in HPLC, GC, UV-Vis spectrophotometry, and other analytical techniques.
• Deep knowledge of GMP, GLP, and regulatory guidelines (USP, EP, BP).
• Skilled in analytical method validation and transfer.
• Experienced in dissolution testing and assay analysis.
• Strong understanding of data integrity principles and ALCOA+ compliance.
• Accurate documentation and review of laboratory records and test reports.
• Effective communication with cross-functional teams (QA, production, R&D).
• Strong attention to detail and commitment to continuous improvement.
• Execute daily operations in compliance with EMS and EHS standards, using appropriate PPE and safe practices.
• Identify, reduce, and prevent environmental impacts and operational risks.
• Contribute to EHS activities, audits, and continual improvement initiatives.

Qualification/Functional Knowledge

• Bachelor's degree in pharmacy/science.
• Proficient with computer software application.
• Minimum 3-6 years' experience in the same field.

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