Specialist - QC

Julphar; United Arab Emirates; On-site; AED 100,000 - 201,000; Full time

Job summary

Julphar in the United Arab Emirates seeks a QC Analyst to ensure GLP and GMP adherence, perform chemical and physical analyses, operate QC instruments, and maintain meticulous records. The role includes data entry in SAP, analytical method validation, and support for audits and CAPAs.

The ideal candidate holds a Bachelor’s degree in pharmacy or science with 3–6 years of relevant experience in a pharma QC environment, and a strong commitment to data integrity and regulatory compliance.

Qualifications

• Bachelor’s degree in pharmacy or science required.
• Experience in GMP/GLP environments is essential.
• Proficient with QA/QC documentation and record-keeping.

Responsibilities

• Ensure GLP, GMP, safety procedures and maintain hygienic lab conditions.
• Carry out chemical and physical analysis of finished/ raw material and stability.
• Operate QC equipment as per section assignment.
• Record all analytical data accurately.
• Enter analysis data into SAP.
• Ensure final products meet specifications and regulatory requirements.
• Adhere to SOPs and assist audits; address observations.
• Manage CAPAs, AMS, and change controls in the quality system.
• Maintain data integrity and good documentation practices in QC labs.
• Support problem solving and troubleshoot day-to-day operations.
• Assist supervisors and delegates in assigned tasks.

Skills

GMP/GLP knowledge

Data integrity

Analytical method validation

Auditing

Documentation & data recording

Cross-functional communication

Troubleshooting

EMS & EHS compliance

Education

Bachelor’s degree in pharmacy/science

Tools

SAP

HPLC

GC

UV-Vis

Job description

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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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