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  5. Production Team Leader

Production Team Leader

  • Julphar
  • Ras Al Khaimah, United Arab Emirates
  • Posted 18 Oct
  • Verified source
Job type
—
Work mode
—
Seniority
Lead
Salary
Not stated

Summary

Julphar is hiring a Production Team Leader for its OSD plant in Ras Al Khaimah, United Arab Emirates. The role oversees granulation, compression, coating and packaging, production schedules, material coordination, product quality and staff training. The successful candidate will support GMP and regulatory compliance, documentation, audit readiness, equipment performance and process improvements. Applicants should have a B.Pharm, M.Pharm, M.Sc. in Pharmaceuticals or Chemistry, or a related degree, with 6–10 years of OSD manufacturing experience, including 2–3 years in a supervisory or managerial role; shift work may be required.

The posting

As published on julphar.net. Pulled from the employer's site and shown as they wrote it.

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 Summary:

The Team Leader in the OSD plant is responsible for overseeing and managing production activities,S 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.

Key Responsibilities:

1. Production Management

  • Supervise and manage the OSD production process, including granulation, compression, coating, and packaging.
  • Ensure adherence to production schedules and optimize output while maintaining product quality.
  • Coordinate with the supply chain, planning, and warehouse teams to ensure smooth material availability.
  • Troubleshoot production-related issues and implement corrective and preventive actions (CAPA).

2. Compliance & Quality Assurance

  • Ensure all operations comply with cGMP, WHO, 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 activities.
  • Maintain proper documentation in accordance with regulatory and company standards.

3. Team Management & Training

  • Supervise and mentor production 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.

4. Equipment & Process Optimization

  • Ensure the proper functioning, calibration, and maintenance of production 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.

5. 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.

6. 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.

Qualifications & Experience:

  • 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.

Work Environment & Additional Information:

  • 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. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar

View the original posting

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Closes in

2288days0077hrs0033min5577sec

Closes in 4 weeks, Sunday, November 15 · end of day.

Sunday, November 15 · end of day

Posted Oct 18, 2026Nov 15, 2026

Skills

  • GMP
  • Leadership
  • Process Improvement

Julphar

Healthcare

All jobs at Julphar

ReferenceGH 693F 5236 DFA8

Always check the employer's original posting for details.

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