Specialist - Lactam

Job Description

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

• SOP related documentation write, review/approve on periodic revisions basis or as on demand situations to comply with audit observations, CAPA / Change controls / deviations compliance.
• Preparation and review of protocols and reports for inhouse studies, developmental activities related to process.
• Strict adherence to data integrity and to follow the ALCOA principles and good documentation practices.
• Responsible to adhere with cGMP principles and maintain them in an effective manner.
• Ensure compliance to implemented quality system.
• Handling the production team, appraisals, annual reviews, assigning duties,
• Prepare and control Monthly overtime and Following up the weekly shift change.
• Prepare and follow the yearly OJT
• Perform on Job Training (OJT) for production staff as per schedule.
• Review and sign in batch documents and checks all related logbooks and records.
• Handling the SAP related activities such as production module/Gl/reservations/Consumable reservations/PR generations as per situational demands.
• Manage department resources in a cost-effective manner to achieve company goals
• Following up the attendance, Leaves, shift planning and documents related to staff.
• Coordinate with Julphar Training Centre regarding basic cGMP and other training.
• Prepare and following the yearly OJT for staff.
• Prepare and Review BMR, SOPs, validation documents
• Ensure area readiness to pass all internal and external inspections
  
  

Core Competency

• Good on Process compliance & implementation skill
• strong understanding and practice of cost consciousness
• Good Command in English
• High on Accountability & Ownership
• Good in team building, Time & Task Management.
• Disciplined, Open for new learnings at the workplace.
  
  

Qualification/ Functional Knowledge

• Pharmacist or related field
• Proficient with computer software application.
• Good Knowledge of cGMP and GDP in manufacturing area.
• Effective manpower and resources handling.
• Proven Experience in pharmaceutical industry
  
  

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

Job Details

Role Level: Mid-Level Work Type: Full-Time Country: United Arab Emirates City: Ras Al Khaimah Company Website: http://www.julphar.net Job Function: Others Company Industry/

Sector: Pharmaceutical Manufacturing

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