Title: Senior Specialist - Quality Control

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 adhere with the cGMP principles and to maintain them in an effective manner.
Responsible to follow up chemical and physical analysis of finished products/ Raw &Packaging Materials
Supervising and follow up analysts, instrumental and physical lab in QC.
Supervising analysts results of FP/RM/PM.
Supervising and follow up analyst instrumental and physical lab in QC department
Responsible for the operation of various QC equipment (depending on the section he working)
To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.
Training newly joined staff
Entering and checking data of analyst on SAP
Assist in trouble shooting and solving problems that may come up in the day to day operation of the department.
Ensure Final Products adhere to all specifications and regulations.
Create HPLC & GC analytical methods from approved STM/Pharmacopoeia for all analysts before start analysis
Processing and approve for all HPLC &GC analytical data for all analysts, review and check all the Audit trial for all the instruments.
To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.
To ensure the analysis are performed correctly as per applicable procedures
To perform investigation for the lab incidents, OOS, OOT results, deviations and take appropriate corrective and preventive actions.
To lock the results in SAP, to create notifications & reservations for maintaining enough stock of chemicals & consumables.
To involve and support in external and internal audits and to close the audit observations on time.
Review and approve protocols and reports such as method validation, method transfer, process validation and stability.
To handle and close the Quality management system actions like Deviations, OOS, CAPAs, AMS and Change controls using Amplelogic system.
To follow and ensure data integrity and good documentation practices are implemented in the QC labs.
Apart from above, the works assigned by the Head of the department/designee.

Core Competency:

Solid Technical knowledge with strong implementation skill, people management skill.
High on communication and collaboration, having an ability to manage multiple stakeholders at a time.
In terms of competency you are highly result oriented with strong sense of accountability & ownership.
In-depth knowledge of the industry’s standards and regulations guidelines excellent knowledge of reporting procedures and record keeping
Methodical and diligent with outstanding planning abilities an analytical mind able to “see” the complexities of procedures and regulations.
Excellent communication skills.
Business acumen partnered with a dedication to legality.
Must be able to manage tasks and priorities and easily adapt to changing situations.
Good command in English (Communication, writing and speaking)
KPI management, proven experience in conducting Risk Assessments.
Problem Solving and high agility on taking right scientific decisions.

Qualification/Functional Knowledge:

Bachelor’s degree in Pharmacy/Science.
Minimum 2 years’ experience in the same field.
Proficient with computer software application.

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.

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