JT123 - MAINTENANCE TECHNICIAN

West Greenwich, RI

Temporary

Biopharmaceutical

Mid Level

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:

F&E Equipment group is responsible for the end to end life cycle of equipment in QC.
This includes procurement, development, and execution of validation and change control strategy, oversight and execution of general and preventative maintenance activities, and decommissioning support as required.
Execute routine work orders and interact routinely with end customers and vendors, ensuring reliable equipment support in a fast-paced environment.
Own change controls for new and/or replacing of equipment.
Manage the procurement of new QC equipment. Work autonomously to lead cross-functional stakeholders to identify end-user requirements, establish validation requirements and Change Control strategy.
Monitor and trouble shoot analytical benchtop equipment.
Lead projects and project planning responsibilities to ensure on time implementation of analytical instruments. Responsible for implementing projects on time and on budget.
Complete all assigned tasks on time, in collaboration with key stakeholders.
Provide oversight of vendor PMs.
Create new assets and PM scheduling in Maximo.
Obtain end user requirement and vendor quotes for lifecycle replacement of equipment.

Qualifications:

Associate degree and 2 years of experience OR 2 years in a technical school setting with hands-on experience OR High school diploma / GED and 4 years of experience
Experience in writing and managing Change Controls
Experience in executing general, preventative, and corrective maintenance in Maximo system.
Validation experience (Lab equipment, computer related systems)
Focus on data integrity and cGMP practices
Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.
GMP and GDP experience in a laboratory setting.
Proficient in Trackwise, Maximo, CDOCS
Experienced in Quality systems, including Change Control, Deviations, CAPA
Experienced in Quality processes, including validation and data integrity
Proficient in problem solving and LEAN principles
Commitment of 40-hour work week in West Greenwich, RI.
Fully Onsite
Working Schedule: 8AM - 5PM

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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