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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, 7a-3:30p

+ After training, shift schedule is 12-hour days working 3-4 days per week 6am-6:30pm.

+ Workers should be flexible within day shift hours.

+ Potential overtime opportunities

+ Day 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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