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:
Support the maintenance, operation, and repair of all manufacturing equipment within the client's facility
Provide support to engineering and operations in the design, installation, testing, operation, and maintenance of manufacturing and support equipment
Ensure all assigned equipment and associated subsystems are maintained in accordance with Federal, State, Local, and client's regulations, procedures, and policies
Maintain all assigned equipment areas in a constant state of inspection readiness
Identify training deficiencies and provide recommendations and training where applicable
Continuously evaluate and improve maintenance practices and documentation
Perform troubleshooting of electrical, pneumatic, and mechanical equipment
Complete preventive maintenance and assigned paperwork following all cGMP documentation guidelines
Coordinate contractors for repairs, modifications, and installations of equipment
Work directly with Manufacturing, Engineering, and Quality organizations on new system installations or modifications
Attend all required cGMP and Safety training
Qualifications:
Associate degree and 4 years of experience
Minimum of 2+ years of experience in manufacturing maintenance is ideal.
Mechanical maintenance experience in a manufacturing environment
Thorough working knowledge of pharmaceutical packaging equipment operation, maintenance, and repair
Full working knowledge of pumps, valves, motors, and proper lubrication
Strong documentation and attention to detail
Full working knowledge of cGMP and Predictive Maintenance philosophy and techniques
Ability to create, read, interpret, and revise engineering documents
Strong writing skills for preparing technical reports and documentation
Ability to identify and implement process improvements
Ability to read and understand P&IDs, work from SOPs, and use basic computer skills
Knowledge of and ability to use Computerized Maintenance Management Systems (Maximo)
Detail-oriented and organized with good record-keeping practices
Effective communication skills and ability to work with minimum supervision
Capable of multi-tasking and working overtime or temporarily modifying shift schedule as needed
Ability to lift up to 50 pounds, climb ladders, and work at elevations up to 15 feet
Experience with CMMS programs, writing work orders, documenting troubleshooting steps, etc.
2-3month training period, 8hr days, 7am-3:30pm
After training, shift schedule is 12-hour days working 3-4 days per week 6pm-6:30am.
Workers should be flexible within day shift hours.
Potential overtime opportunities
Night 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.