OSD Production Lead & GMP Compliance Expert

Julphar

Ras Al Khaimah

On-site

AED 201,000 - 335,000

Full time

31 hours ago
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Job summary

Julphar in Ras Al Khaimah seeks a Senior Specialist/Team Leader for the OSD plant to lead production/packaging, ensure GMP compliance, and drive cross-functional coordination. The role requires overseeing CAPA, deviations, and batch documentation to maintain quality and regulatory readiness.

The incumbent will supervise operators and technicians, train staff on SOPs and safety, and partner with QA, R&D, engineering, and regulatory teams to optimize processes and ensure efficient production while

Qualifications

  • Education: B. Pharm / M. Pharm / M.Sc. in Pharmaceuticals, Chemistry, or related field.
  • Experience: 6-10 years in OSD pharmaceutical manufacturing, with at least 2-3 years in a supervisory or managerial role.
  • Knowledge & Skills: GMP, regulatory compliance, and safety guidelines; experience with OSD equipment like granulators, tablet presses, coating machines, and blenders; leadership and strong communication and documentation skills.

Responsibilities

  • Oversee and manage OSD production/packaging processes; ensure schedules, output, and quality.
  • Ensure compliance with cGMP, WHO, FDA/foreign regulatory standards; maintain in-process quality checks and document deviations.
  • Supervise packaging staff, conduct SOP/GMP training, and monitor performance for continuous improvement.
  • Maintain equipment calibration and maintenance; identify process improvement opportunities and collaborate with engineering/maintenance.
  • Ensure safety compliance and waste handling per regulatory norms; conduct risk assessments and preventive actions.
  • Prepare plant for regulatory inspections and customer audits; manage batch records and validation protocols.

Job description

Julphar in Ras Al Khaimah seeks a Senior Specialist/Team Leader for the OSD plant to lead production/packaging, ensure GMP compliance, and drive cross-functional coordination. The role requires overseeing CAPA, deviations, and batch documentation to maintain quality and regulatory readiness.

The incumbent will supervise operators and technicians, train staff on SOPs and safety, and partner with QA, R&D, engineering, and regulatory teams to optimize processes and ensure efficient production while

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