2.0 Key Responsibilities and End Results: (Essential responsibilities include but are not limited to the following):

• To maintain automation equipment in excellent condition ensuring consistent quality, output and yield.

• Follow systematic root cause problem solving and troubleshooting to resolve issues.

• Carry out preventative and corrective maintenance, completing all associated paperwork and records.

• Lead and implement process improvements to achieve more efficient operations, while adhering to

change management and cGMP requirements.

• Assist with the commissioning of new equipment / projects.

• Order and maintain appropriate stock of spare parts.

• Cross Train technicians as required.

• Flexible to travel to support new equipment buy-offs / training.

• Support all company safety and quality programs and initiatives.

• Ensure ongoing compliance with GMP in all practices, recording of events and processes.

• Ensure compliance with all learnings from all GMP training events.

• Other responsibilities may be assigned from time to time as needed, based on the evolution of the

company and the requirements of the department/position.

Skills/Attributes:

• Systematic & structured troubleshooting / problem solving skills.

• Ability to provide innovative solutions to complex technical problems.

• Adherence to change management procedures and cGMP requirements.

• Good written and oral communication skills.

• Ability to work well in a team environment.

• High level of safe working practices and awareness.

• Computer literate with MS Office skills.

Job Specifications:

• The successful candidate will have Level 6, Level 7 or Level 8 HETAC qualification in Manufacturing

Technology, Mechanical / Automation Engineering, Electrical, Electronics, Mechatronics or similar.

• Qualified trades personnel with industrial experience will also be considered.

• Experience in high volume automation / robotics required.

• Experience in a Healthcare medical device manufacturing environment highly desirable.

• Experience in Pneumatics, Electronics, Hydraulics, Programmable Controllers, Servo Motor drives, Vision

systems, Ultrasonic welding, workshop machining desirable.

• Understanding of Process Capability.

• Understanding of MSA or GR&R.

• Experience in leading process improvement projects in medical device environment.

• Experience in FAT, SAT, IOPQ of automated assembly lines.

Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.

BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil.com e-mail address; direct phone call from a member of the Jabil team; or direct e-mail with a jabil.com e-mail address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number, birth certificate, financial institution, driver's license number or passport information over the phone or via e-mail. If you believe you are a victim of identity theft, contact your local police department. Any scam job listings should be reported to whatever website it was posted in.

Accommodation Statement

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to Always_Accessible@Jabil.com with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.

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