Specialist – Quality Control

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** Location** | Ras Al Khaimah, Ras al-Khaimah, United Arab Emirates ||
** Qualifications** | Bachelor’s Degree ||
** Experience** | 2 Year+ |## Job Overview 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.## Company Overview Julphar is on a journey of culture transformation with a mission to provide a better quality of life by delivering best in class solutions and real value with compassion and professionalism.

The company focuses on diversity, inclusion, and equal opportunities to make a positive impact on the lives of patients and create a healthy work environment.## Quick Details
* Salary Range:
Market Competitive
* Job Type: Full-time

* Qualifications:

Bachelor’s degree in pharmacy/science

* Experience:

2 years’ experience in the same field##

Key Responsibilities
* Adhere to cGMP principles and maintain them effectively.
* Carry out chemical and physical analysis of finished products, raw materials, and stability samples, as well as process validation.
* Operate various QC equipment and follow GLP, GMP, and safety procedures.
* Enter data on SAP and maintain accurate records of all working data.
* Create HPLC & GC analytical methods and process analytical data.
* Perform investigations for lab incidents, OOS, OOT results, and deviations.## Requirements
* Bachelor’s degree in pharmacy/science.
* Minimum 2 years’ experience in the same field.
* Proficient with computer software applications.
* Strong communication, interpersonal, and problem-solving skills.
* High on process compliance and implementation skills with strong attention to details.## Benefits
* Opportunity to work with a company focused on innovation and quality.
* Be part of a team committed to making a positive impact on patients’ lives.
* Work in a healthy and inclusive work environment.
* Develop skills in pharmaceutical manufacturing and quality control.
* Gain experience with cGMP principles and SAP.
* Exposure to internal and external audits.
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