Tech 2, Maintenance

Overview

Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO

The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki.

 

Join us

 

We are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America.

The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States.

External US

About This Role

 

The Technician 2, Maintenance is responsible for the installation, maintenance, and repair of process related systems/equipment. Ensure these systems meet the stringent requirements of pharmaceutical manufacturing. Also responsible for conducting regular inspections and preventive maintenance on process related equipment to ensure equipment is operating efficiently with minimal downtime.

 

What You’ll Do

 

• Performs preventative maintenance and repairs on process equipment, such as bioreactors, centrifuges, ultrafiltration skids, parts washers, autoclaves, isolators, and fillers• Provides recommendations to develop preventative maintenance plans to minimize equipment downtime• Contributes to Standard Operating Procedure (SOPs) development and revisions for process maintenance related activities• Diagnoses and troubleshoots equipment malfunctions• Assists in the installation and commissioning of new equipment• Maintains accurate maintenance records and documentation• Follows SOPs to ensure compliance with safety and Good Manufacturing Practices (GMP) quality standards• Adheres to all safety requirements and follows safe work practices• Notifies management or Environmental, Health & Safety (EHS) when unsafe conditions or hazards are found• Attends all required safety and health training• Supports site operations and emergency work orders during off-hours, as needed• Performs spare parts assessments, as required• Other duties, as assigned

 

Who You Are

 

You are able to work cross functionally with other maintenance and technical trades, such as manufacturing operators, engineers, spare parts coordinators, validation, quality, and external suppliers. You have the ability to provide input and recommendations for written instructions on Preventative Maintenance tasks and SOPs. You enjoy training and mentoring entry-level technicians. You are willing to learn and develop new skills related to the maintenance of pharmaceutical production processes.

 

Basic Requirements

• High School Diploma/GED
• 4 years of maintenance experience in a pharmaceutical or similar manufacturing setting
• Experience with Computerized Maintenance Management Systems (CMMS)

Preferred Requirements

• Associates degree in Mechanical, Electrical, Chemical Engineering or a related field
• 5+ years of maintenance experience in a pharmaceutical or similar manufacturing environment
• Certified Maintenance & Reliability Professional, Certified Maintenance & Reliability Technician or certification in another relevant field

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

 

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.  While performing the duties of this job, the employee is regularly required to:

• Experience prolonged sitting, standing, walking, bending, stooping, and stretching.
• Use hand-eye coordination and manual dexterity sufficient to operate portable tools, test instruments, as well as a computer keyboard, telephone, calculator, an