Sr. Specialist

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.

The Sr. Specialist/Team Leader in the OSD plant is responsible for overseeing and managing production/Packaging activities, ensuring compliance with GMP, regulatory guidelines, and safety protocols. The role involves coordinating with cross-functional teams to achieve production targets, maintaining product quality, and optimizing operational efficiency.

• Production/Packaging Management
• Supervise and manage the OSD production/Packaging process, including granulation, compression, coating, and packaging.
• Ensure adherence to production/packaging schedules and optimize output while maintaining product quality.
• Coordinate with the supply chain, planning, and warehouse teams to ensure smooth material availability.
• Troubleshoot production/packaging-related issues and implement corrective and preventive actions (CAPA).
• Compliance & Quality Assurance
• Ensure all operations comply with cGMP, WHO, SFDA, USFDA, MHRA, and other regulatory standards.
• Work closely with the Quality Assurance (QA) team to ensure in-process quality checks.
• Handle deviations, change controls, and investigations related to production/packaging activities.
• Maintain proper documentation in accordance with regulatory and company standards.
• Team Management & Training
• Supervise and mentor production/packaging staff, including operators, technicians, and junior executives.
• Conduct training programs on SOPs, GMP guidelines, and safety procedures.
• Monitor employee performance and provide feedback for continuous improvement.
• Equipment & Process Optimization
• Ensure the proper functioning, calibration, and maintenance of production/packaging equipment.
• Identify opportunities for process improvements and cost reduction while maintaining quality.
• Collaborate with the engineering and maintenance teams for timely resolution of equipment issues.
• Safety & Compliance
• Ensure adherence to workplace safety guidelines and implement safety measures.
• Conduct risk assessments and take necessary preventive actions to minimize hazards.
• Ensure proper handling and disposal of waste as per environmental and regulatory norms.
• Regulatory & Audit Readiness
• Prepare the plant for regulatory inspections and customer audits.
• Ensure timely completion of all documentation, including batch manufacturing records (BMR), standard operating procedures (SOPs), and validation protocols.
• Address audit findings and implement corrective measures.

• Education:
  
  B. Pharm / M. Pharm / M.Sc. in Pharmaceuticals, Chemistry, or related field.
• Experience:
  
  6-10 years of experience in OSD pharmaceutical manufacturing, with at least 2-3 years in a supervisory or managerial role.
• Knowledge &
  
  Skills:
  • Strong understanding of GMP, regulatory compliance, and safety guidelines.
  • Experience in operating and troubleshooting OSD equipment like granulators, tablet presses, coating machines, and blenders.
  • Leadership and team management skills.
  • Excellent problem-solving and decision-making abilities.
  • Strong communication and documentation skills.

• The role requires working in a controlled manufacturing environment.
• May involve working in shifts, depending on production needs.
• Requires collaboration with QA, R&D, engineering, and regulatory teams.

We value people from different backgrounds.