Sr Maintenance Engineer (GMP, M&E, Pharmaceutical, Office hours 5 days)

Sr Maintenance Engineer (GMP, M&E, Pharmaceutical, Office hours 5 days)

Job Description

• Monitor and supervise mechanical work activities.
• Propose and make improvements of upgrading work.
• Troubleshooting of plant equipment.
• Plan and proposal for plant equipment replacement work.
• Prepare work specifications and documentation for projects and upgrading work.
• Coordinate all project activities from design to production stage with contractors.
• Coordinate and supervise all related work with contractors.
• Coordinate Computerised Maintenance Management System (CMMS) activities for preventive maintenance.
• Organise maintenance activities and maintenance equipment in good condition.
• Motivate and co-operate with team members.
• Documentation record for Good Manufacturing Practice (GMP).
• Do risk assessment and safety awareness for team members.
• Scope, plan and execute multiple projects simultaneously.
• Supervise one or more highly technical personnel that resolve equipment operational issues; investigate, complete CAPA’s and remediate audit observation response items.
• Support investigations, participate and complete corrective actions/preventative actions (CAPA’s) based on root cause analysis and remediate audit observation response items.
• Support risk management initiatives to ensure organizational strategic objectives in the areas of asset capability, quality and production.
• Conducts Root Cause Analysis (RCA) or Root Cause Failure Analysis (RCFA).
• Troubleshoot complex systems.
• Develop required training and standards.
• Develop engineering solutions to improve the operational efficiency and uptime of production equipment.
• Work with equipment manufacturers to improve and upgrade equipment.
• Understand functionality and be familiar with computerized maintenance management system or asset management systems.

BASIC QUALIFICATIONS

• Bachelor’s degree in an engineering discipline or similar / equivalent discipline is required.
• A minimum of 3 years of experience in a sterile or pharmaceutical environment is required.
• Engineering knowledge in one or more of the following: Electrical, Mechanical, Automation, Statistics, Maintenance, Reliability and Quality.
• Excellent written, communications and presentation skills.
• Possess good analytical and computer skills.
• Have a thorough understanding of cGMP's.
• Able to perform mathematical calculation and have the ability to perform complex data analysis.

PREFERRED QUALIFICATIONS

3 years of experience in a sterile or pharmaceutical environment is preferred.