Lead Manufacturing Engineering Technician

Job Description :

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Alignment with all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair, etc., are not permitted. Some level of PPE (Personal Protective Equipment) is necessary (safety glasses, gowning, gloves, lab coat, ear plugs, etc.).

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit

Roles And Responsibilities

• To support and provide problem-solving effort that is related to instrument issues to identify root cause, evaluate alternative solutions, and develop action plans. We support third-party vendor who is contracted to perform routine calibration, preventive maintenance, corrective maintenance and any other maintenance related activity.
• Complete the routine maintenance works as scheduled and in compliance with Engineering standards and safety procedures.
• All GMP documentation related to maintenance activities is completed accurately and processed to full completion in compliance to data integrity requirement.
• Complete training provided to build-up the competencies. Comply to the instrument maintenance procedures/SOPs and good documentation system to ensure quality assurance operations.
• Available for on-call duty and willing to work extra hours as needed to support ongoing operations.
  

Education

• NITEC or Diploma in Engineering related qualifications. Preferably in Electrical or Electrical & Electronics Engineering or Instrumentation.
  

Experience

• Minimum 5 years with meaningful experiences in pharmaceutical industry.
• Ability to read PID drawing, Instrument loop drawing and instrument panel drawing.
• Proficient in oral and written English. Proficient in operating within a fast-paced and regulated environment.
• Experience in solving field instrumentation and automation systems issues.
• Experience in PLC, SCADA and HMI panel operations will be added advantage.
  

Knowledge, Skills, Abilities

• Knowledge in Calibration Processes and basics of Automation System.
• Strong understanding of facilities systems related validation / GMP requirements.
• Strong ability to fix issues and a good knowledge of different RCA tools.
• Good interpersonal skills and collaboration.
• Able to work independently and diligent in performing operational checks.