Specialist - Lactam

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
  
  

• 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.
  
  

• 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