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Home/Jobs/Process Equipment Supervisor
Eva Pharma logo
Eva Pharma

Process Equipment Supervisor

🇸🇦 Riyadh, Saudi Arabia🏢 On-site
Process EquipmentMaintenancePharmaceuticalGxPMechanicalElectricalSupervision
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Eva Pharma
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Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as the best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary

We are seeking a passionate and talented (Process Equipment Supervisor) to join our dynamic team.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities:

• Manage/supervise the process equipment maintenance team of multi skill technicians, senior technicians under assigned section (dose form/scope of line as per Organization chart).
• Engage self and team to deal with day-to-day routine maintenance and troubleshooting of operational issues in production area equipment to ensure daily production targets are as per schedule.
• Being engaged for all new process equipment specifications setting, factory acceptance test and site acceptance tests, including and not limited to technical handover and training during commissioning.
• Professional serialization and aggregation including advanced automated systems configuration and troubleshooting.
• Prepare and execute documented maintenance work plans, equipment maintenance SOPs, planned preventive maintenance in respective assigned areas.
• Conduct the risk-based maintenance requirement assessment for major/ planned maintenance with all safety measures in place. Maintain, update and review CDA and PM Plan.
• Carry out spare parts assessment and maintain spare parts inventory effectively, including GxP Spares. Ordering, follow up and receipt of spares and lubricants as stated in SOPs.
• Investigate, identify and document the root cause of breakdowns for all GxP/ EHS/ Business critical equipment through structure problem solving approach (5W1H, 5why/Fishbone, CAPA). Requirements

• E/BS/High Institution (Mechanical/Industrial/Electronics/Electrical).
• Not Less than 7 year experience in Pharmaceutical / Packaging industry with at least 5 year role of hands on maintenance work and 02 years in supervision of technical team at Pharmaceutical/FMCG production process Industry.
• Strong supervisory skills in dealing with multi-skill team with evolving progress as Manger.
• Competencies through proven knowledge and experience to deal with maintenance of Pharmaceutical manufacturing & Packaging equipment covering all technical aspects (mechanical, electrical, electronic controls, hydraulics, data management).
• Good in problem solving, communication, and team-working skills.

Requirements

  • •Bachelor's degree in Mechanical/Industrial/Electronics/Electrical Engineering
  • •Not less than 7 years experience in Pharmaceutical/Packaging industry
  • •At least 5 years hands-on maintenance work
  • •At least 2 years in supervision of technical team
  • •Strong supervisory skills
  • •Knowledge of maintenance for Pharmaceutical manufacturing Packaging equipment
  • •Good problem solving, communication, and team-working skills

Nice to Have

  • •Engage for all new process equipment specifications setting, factory acceptance test and site acceptance tests
  • •Professional serialization and aggregation including advanced automated systems configuration and troubleshooting
  • •Ordering, follow up and receipt of spares and lubricants as stated in SOPs

Responsibilities

  • •Manage/supervise the process equipment maintenance team
  • •Deal with day-to-day routine maintenance and troubleshooting
  • •Ensure daily production targets are met
  • •Prepare and execute documented maintenance work plans
  • •Conduct risk-based maintenance requirement assessment
  • •Maintain, update and review CDA and PM Plan
  • •Carry out spare parts assessment and maintain spare parts inventory
  • •Investigate, identify and document the root cause of breakdowns

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