HOD - Sterile

Date: Apr 3, 2025

Location: Ras Al khaima, United Arab Emirates

Company: Julphar

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.

 

Specific Job Description:

 

  • Oversee all aspects of production within the Sterile value stream, including both plants J2 and J8.
  •  Support the implementation of the strategic plans to optimize production efficiency and meet operational goals.
  •  Ensure compliance with regulatory standards, particularly GMP (Good Manufacturing Practices), and other relevant guidelines.
  •  Lead and manage cross-functional teams to achieve operational excellence and continuous improvement.
  •  Manage operational budgets and resources effectively to support production schedules and strategic initiatives.
  •  Foster a culture of quality, safety, and compliance throughout the value stream.
  •  Monitor and report on key performance indicators (KPIs) to track progress and identify areas for improvement.
  •  Collaborate with other departments such as Quality Assurance, Regulatory Affairs, and Supply Chain to ensure seamless operations and alignment with organizational objectives.
  •  Provide leadership and mentorship to team members, promoting professional development and engagement.
  •  Implement best practices in pharmaceutical manufacturing.

 

Core Competency:

 

  • Expertise in pharmaceutical manufacturing operations, specifically in sterile processes.
  • Strong understanding and application of GMP regulations and quality standards.
  •  Proven leadership ability to drive cross-functional teams and achieve operational goals.
  •  Strategic thinker with the ability to optimize production efficiency and implement continuous improvement initiatives.
  •  Excellent communication skills with the capacity to foster a culture of quality, safety, and compliance.
  •  Effective budget management and resource allocation to support operational objectives.

 

Qualification/Functional Knowledge:

 

  • Postgraduate in Pharmacy, Engineering or any related scientific discipline, with a strong understanding of pharmaceutical processes and regulations.
  • Minimum of 10 years of experience in a similar role within pharmaceutical manufacturing, with a track record of leadership and achievement.
  •  Proven ability to manage multiple tasks and priorities effectively in a fast-paced environment.
  •  Familiarity with regulatory requirements in core markets, including USFDA, MOHAP, and other relevant agencies.
  •  Strong analytical and problem-solving skills to address complex operational challenges.
  •  Excellent communication and interpersonal skills to lead cross-functional teams and collaborate effectively.
  •  Strategic mindset with the ability to drive continuous improvement initiatives and achieve operational excellence.
  •  Experience in budget management, resource allocation, and performance management within a regulated manufacturing environment.

 

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