Sr. 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.Job Summary/Main PurposeThe 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. The Specialist operates various QC equipment, follows GLP, GMP, and safety procedures, and maintains hygienic conditions in the lab. Additionally, the Specialist is responsible for entering data on SAP, recording all working data, assisting supervisors, training newly joined staff, and ensuring final products adhere to all specifications and regulations. The role also includes creating and processing HPLC & GC analytical methods, performing investigations for lab incidents, and supporting external and internal audits.Key ResponsibilitiesTo adhere with the cGMP principles and to maintain them in an effective manner.Responsible to carry-out chemical and physical analysis of FP/RM/Stability, process validation.Responsible for the operation of various QC equipment (depending on the section).Follow GLP, GMP and safety procedures and maintain hygienic conditions in lab.Enter data on SAP.Responsible for recording all working data.Help supervisors in assigned tasks.Ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.Training newly joined staff.Enter and check data of analyst on SAP.Assist in trouble shooting and solving problems that may arise 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/Pharmacopeia for all analysts before starting analysis.Process and approve all HPLC & GC analytical data for all analysts, review and check all audit trails for all instruments.Train the QC personnel on all applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.Ensure the analysis is performed correctly as per applicable procedures.Perform investigations for lab incidents, OOS, OOT results, deviations and take appropriate corrective and preventive actions.Lock results in SAP, create notifications & reservations to maintain enough stock of chemicals & consumables.Involve and support external and internal audits and close audit observations on time.Review and approve protocols and reports such as method validation, method transfer, process validation and stability.Handle and close the quality management system actions like deviations, OOS, CAPAs, AMS and change controls using Amplelogic system.Follow and ensure data integrity and good documentation practices are implemented in the QC labs.Apart from the above, perform works assigned by the Head of the department/designee.Core CompetencyHighly oriented with strong sense of accountability & ownership.High on process compliance and implementation skills with strong attention to details.Strong communication, interpersonal and problem‑solving skills.Business acumen partnered with dedication to legality.Ability to manage tasks and priorities and adapt easily to changing situations.Highly disciplined, organized, self‑motivated to learn new skills and implement them at workplace.Can work in a cross‑functional environment interacting with other internal and external departments.Qualifications, Key Experiences / Functional Knowledge RequirementsBachelor’s degree in pharmacy or science.Minimum 2 years’ experience in the same field.Proficient with computer software applications.Adherence to cGMP principles and maintaining them effectively.Conduct chemical and physical analysis for RM, FP and stability.Operate various QC equipment and ensure compliance with GLP, GMP, and safety procedures.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.#J-18808-Ljbffr