Lead Manufacturing Engineering Technician

at  Thermo Fisher Scientific

JOB DESCRIPTION

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 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, improving patient diagnostics and therapies or growing efficiency in their laboratories, we are here to support them. Our distributed team of more than 75,000 colleagues delivers an outstanding 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 and Patheon. For more information, please visit www.thermofisher.com.

POSITION SUMMARY

The incumbent will support site wide routine operation and preventive maintenance, ad-hoc corrective maintenance to process equipment, utilities and facilities system. The incumbent may also be required to support equipment / instrument calibration and performance. Aligning with cGMP, EHS, Data Integrity, and regulatory requirements is a must for all tasks.

Minimum Requirements/Qualifications

• NITEC or Diploma in Engineering related qualifications
• Minimum 5 years with experience in the pharmaceutical industry, biopharma, and medical devices.
• Strong understanding of facilities and utilities systems and process equipment related validation / GMP requirements.
• Strong electrical knowledge is essential
• Safety certificates, example, confined space, will be advantage

RESPONSIBILITIES

• Participate in problem solving discussions with multi-functional team to identify/define root cause, evaluate alternative solutions, and develop action plans.
• Execute the routine maintenance for the site utilities systems, production equipment, control systems, automated filling lines, packaging etc in a timely manner and in compliance with Engineering standards and safety procedures.
• Complete training provided timely to improve proficiencies.
• Contribute to team effort by achieving desired results/important metrics. Share Knowledge and mentor colleagues to build up their proficiencies.
• Manage third-party vendor who is contracted to perform routine preventive maintenance, corrective maintenance and any other maintenance related activity.
• Ensure all GMP documentation related to maintenance activities is completed accurately and processed to full completion in compliance to data integrity requirement.
• Carry out any other duties and responsibilities as assigned by supervisor, including but not limited to the above.

Minimum Requirements/Qualifications

• NITEC or Diploma in Engineering related qualifications
• Minimum 5 years with experience in the pharmaceutical industry, biopharma, and medical devices.
• Strong understanding of facilities and utilities systems and process equipment related validation / GMP requirements.
• Strong electrical knowledge is essential
• Safety certificates, example, confined space, will be advantage.