Specialist - QC

Julphar; United Arab Emirates; On-site; AED 150,000 - 190,000; Full time

Job summary

Julphar UAE is seeking a skilled QC Analyst to join our pharmaceutical lab. You will perform GLP/GMP compliant analysis of Simi Finished/Raw Material/Stability, operate QC instruments, record data accurately, and ensure final products meet specifications.

You will support internal and external audits, uphold ALCOA+ data integrity, follow SOPs, and collaborate with QA, Production and R&D to drive continuous improvement in quality and safety.

Qualifications

• Bachelor’s degree in pharmacy/science is required.
• Proficient with computer software applications.
• Minimum 3-6 years’ experience in the same field.

Responsibilities

• Perform GLP, GMP, safety procedures and maintain hygienic lab conditions.
• Carry-out chemical and physical analysis of Finished/Raw Material/ Stability.
• Operate QC equipment and record all working data.
• Enter data of analysis on SAP.
• Ensure final products adhere to specifications and regulations.
• Follow SOPs strictly and support audits.
• Handle CAPAs, AMS and Change controls using Ample logic system.
• Maintain data integrity and ALCOA+ compliance.
• Collaborate with QA, production and R&D.

Skills

HPLC

GC

UV-Vis

ALCOA+

GMP/GLP

Analytical methods

Dissolution testing

Audit support

Communication

Problem solving

Education

Bachelor’s degree in pharmacy/science

Tools

SAP

Computer software

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.
• Help supervisors/Designate in assigned tasks.
• 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.

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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