Specialist - Non Sterile
Julphar
Date: 5 hours ago
City: Ras al-Khaimah
Contract type: Full time

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
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
- In this role you will be responsible for adhering to and ensuring compliance with cGMP principles and maintain them in effective manner.
- Perform in-process quality check activities according to SOP in production / packaging departments (Tablets/Capsules/liquids/Semi solids/Injectable) in complying with cGMP principles and captures test results in batch records.
- Check the required tests for all products during production / packaging process.
- Inspect and check incoming materials by confirming specifications and return unacceptable materials.
- Revise all documents for in process control and perform a quality review of logbooks.
- Responsible to revise and document for inspection results and complete all required documents for in process control by completing reports and logs, summarizes re-work and waste, and inputs data into quality database on SAP system.
- Participate in Internal Audit programs.
- Preparation of Annual Product Quality Review reports.
- Responsible for Deviations and Market Complaint investigations and ensure implementation of CAPA lifecycle.
- Ensure the in-process check equipment’s are adequately calibrated and functions properly.
- Perform and check the line before start (production/packaging) and give the clearance for the work.
- Maintain accurate records and perform tests on all activities conducted in the plant.
- Maintain safe and healthy work environment by following standards and procedures and complying with regulations.
- Perform Self-inspection runs in his areas.
- In terms of competency, you are highly result oriented with strong sense of accountability & ownership.
- High on compliance adherence, having strong attention to detail, proactive and flexible
- Good communication, interpersonal, and collaboration skills.
- Should be having good learners mind to understand and grasp new learnings.
- Motivated, organized, focused & overall compliance.
- Must be able to manage tasks, plan workload effectively, priorities and easily adapt to changing situations.
- Ability to understand new learnings and implant in workplace.
- Bachelor’s degree in science/ pharmacy
- Minimum of 2 Years experience
- Good Computer knowledge and knowledge of QMS system “Agile, Trackwise, Ampelogic”
- Proficient in English.
- Quality and Business decisions taker
- Good Knowledge and command on cGMP
- Risk Assessment knowledge
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