Website Julphar
Julphar (Gulf Pharmaceutical Industries) is a public shareholding pharmaceutical company based in Diqdaqah, Ras Al Khaimah, United Arab Emirates. It was established in 1980 under Sheikh Saqr bin Mohammad al-Qassimi, the late ruler of Ras Al Khaimah and currently produces and distributes pharmaceutical products across five continents.
Title: Process Lead – 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.
Job Description
- Responsible for overseeing and leading quality control processes and projects within the department, ensuring that products meet quality standards and regulatory requirements. The role involves process optimization, managing QC projects, and leading a team of QC professionals.
- Develop, implement, and maintain QC processes to improve efficiency and product quality.
- Analyse current QC processes and propose improvements to optimize performance.
- Coordinate with cross-functional teams, including R&D, regulatory affairs, production, and compliance.
- Ensure that all products meet internal and external quality standards.
- Conduct audits and inspections to maintain compliance with regulatory requirements.
- Lead, train, and mentor QC staff to ensure a high level of competency and motivation.
- Analyse quality data to identify trends and areas for improvement.
- Prepare and present reports on QC activities and project progress to management.
- Ensure adherence to industry regulations and standards ( current regulatory & cGMP requirements).
- To adhere with the cGMP principles (premises, personal, equipment, documentation, QMS and audit) and to maintain them in an effective manner.
- To check and ensure proper usage of all the QC equipment.
- To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.
- 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 and the raw data is checked for correctness, accuracy and compliance.
- To perform investigation for the lab incidents, OOS, OOL results, deviations and take appropriate corrective and preventive actions.
- Follow up &Close all the EQMS actions (CAPA, OOS, Deviations, CC)
- To involve and support in external and internal audits and to close the audit observations on time.
- Apart from above, the works assigned by the Head of the department/designee.
- 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.
- To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.
- Shall be authorized designee for responsibilities of QC Sr Manager.
Core Competency
- High on communication and collaboration, having an ability to manage multiple stakeholders at a time.
- Strong eye for details, having expertise to understand, review and implement the compliance inputs from Quality point of view.
- In-depth knowledge of the industry’s standards and regulations guidelines, excellent knowledge of reporting procedures and record keeping.
- Must be able to manage tasks and priorities and easily adapt to changing situations.
- Ability to create cross functional relations and manage conflicts.
Qualification/Functional Knowledge
- Bachelor’s degree in chemistry or pharmacy or any related field.
- Minimum 10 years of experience in QC/QA department
- Proven experience in quality control and/or quality assurance roles, preferably in a leadership capacity.
- Strong knowledge of regulatory requirements and quality standards relevant to the industry.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong leadership and team management capabilities.
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
To apply for this job please visit careers.julphar.net.