Diploma or Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Mechatronics Engineering, Biomedical Engineering, Science, Pharmaceutical Technology or a related field.
Fresh graduates are encouraged to apply.
Candidates with 1–2 years of experience in pharmaceutical, medical device, biotechnology or manufacturing industries will have an added advantage.
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Diploma or Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Mechatronics Engineering, Biomedical Engineering, Science, Pharmaceutical Technology or a related field.
Fresh graduates are encouraged to apply.
Candidates with 1–2 years of experience in pharmaceutical, medical device, biotechnology or manufacturing industries will have an added advantage.
...
To lead, plan and develop departmental goals and objectives for Facilities Department
Responsible in all aspects of building maintenance & renovation including C&S, electrical, ventilating and air-conditioning (HVAC), M&E infrastructure, security and facilities management in a cost efficient & effective manner in line with approved SOPs, regulatory and audit requirements.
Responsible for monitor and track competencies of subordinates and outsource services.
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Objective: To oversee quality, technical, and engineering functions within the organization, ensuring high product standards, efficient processes, and reliable operations while supporting continuous improvement and business objectives.
Key Accountabilities:
To oversee quality assurance to ensure products meet customer and regulatory requirements.
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Objective: To oversee quality, technical, and engineering functions within the organization, ensuring high product standards, efficient processes, and reliable operations while supporting continuous improvement and business objectives.
Key Accountabilities:
To oversee quality assurance to ensure products meet customer and regulatory requirements.
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Conduct comprehensive quality inspections and testing of pharmaceutical products and medical devices at various stages of manufacturing to ensure compliance with established quality standards and specifications
Develop, implement and maintain quality assurance protocols, standard operating procedures (SOPs) and documentation systems in accordance with regulatory requirements and industry best practices
Monitor and analyse quality data, test results and manufacturing records to identify trends, variances and potential areas for improvement
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