QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Repairs and maintains machinery and mechanical equipment such as engines, motors, pneumatic tools, conveyor systems, production machines and other equipment.  

• Operates manufacturing equipment for troubleshooting, repairs, and for functional test purposes.

• Performs all duties with strict observance to cGMP's, cSOP's, cGDP's and other internal and external regulations. 

• Troubleshoots mechanical, electrical and electronic issues.

• Fill out all necessary documentation to comply with Company specifications (SOP's).

• Performs preventive maintenance work and reports according to established standards. 

• Must keep the work area in the cleanest and ordered conditions, following the 6’s concepts

• Responsible for the requesting + replacement of parts, following up on request in a timely manner for assigned equipment.

• Observes mechanical devices in operation and listens to their sounds to locate cause of trouble. 

• Dismantles devices to gain access to and remove defective parts.

• Inspects used parts to determine-changes in dimensional requirements and causes of failure.

• Adjust functional parts of devices and control instruments, Replace or repair defective parts. 

• Installs special functional and structural parts in devices.

• Lubricates and cleans parts.

• Carries tools and equipment to and from storage and working areas. 

Qualifications:

• Associate’s degree in Electronics, Instrumentation (preferred) or Mechanics and

• Zero to five years of experience in related areas.

• Computer literate. 

• Ability to read and interpret documents such as safety rules operating and maintenance instructions, and procedure manuals.

• Ability to write routine reports and correspondence.

• Ability to speak effectively with the immediate supervisor.  Ability to communicate, read, write and understand English/Spanish languages.  

• cGMPs Training, Safety Trainings, certificates, licenses, exams and registrations that the immediate supervisor refers. 

•  Able to follow all GMP requirements while conducting the assigned duties and completing official documents.    

• Able to work extra hours, Holidays (e.g. shutdowns, special projects). 

• Available for 3rd shift.

  Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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