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:- Candidates will be responsible for covering nearby regions and traveling across different areas of the island, visiting hospitals and healthcare facilities throughout Puerto Rico.
- As part of their duties, they will inspect, evaluate, and service infusion pumps, ensuring proper functionality and compliance with established quality and safety standards.
- Installs, checks out, operates, maintains, repairs, and modifies equipment.
- Provides guidance and training to customer personnel in establishing operation, maintenance, and inspection procedures and techniques.
- Analyzes equipment failures to determine cause and recommends corrective action.
- Advice and assists in effecting design changes to improve equipment efficiency and/or reduce cost of operation.
- Devises and implements preventive maintenance programs and keeps performance and maintenance records on equipment.
- Participates in installation planning phase.
- Assists technologists and/or management in evaluation of device problems, procedural issues, and documentation and quality issues.
- Adhere to all environmental, health and safety SOP’s, equipment, policies, and procedures, including any department specific requirements.
- Schedules service calls with customers in accordance with current procedures published by national and regional management.
- Repair devices in accordance with specific documents or SOP’s and complete necessary service documentation.
- Performs tests/diagnoses of systems.
- Identifies and implements corrective actions on processes and non-conformance issues covered by documentation in accordance with Quality/Regulatory requirements.
- Conducts all roles and responsibilities with the ethics and compliance platform.
- Bachelor’s Degree plus 2 years of experience, or associate degree plus 5 years of experience in a related field service, electronics, technical, etc., or In lieu of degree, 5-7 years field service experience.
- Computer Literate.
- Ability to read and comprehend material written in English.
- Problem solving skills.
- Ability to work independently.
- Willing to travel (locally and abroad).
- Overtime may be required at times.
- May require working some holidays and weekends.
- Required have own vehicle.
- Available for 1st shift.
- Monday – Friday, 7:45 AM – 4:45 PM.
- Weekends as needed.
- Car Allowance: up to $600.00.
- Cellphone Allowance: up to $50.00.
Skills Required
- Bachelor's degree plus 2 years of related experience
- Associate degree plus 5 years of related field service, electronics, or technical experience
- Alternatively, 5-7 years of field service experience without a degree
- Computer literacy
- Ability to read and comprehend English-language material
- Problem-solving skills
- Ability to work independently
- Willingness to travel locally and abroad
- Own vehicle
- Availability for first shift, Monday-Friday, 7:45 AM-4:45 PM
- Availability for overtime, weekends, and holidays as needed
What We Do
The Quality Consulting Group is a pharmaceutical, biotechnology, food and medical device specialty consultant that supports the manufacturing industry; services are provided in multiple areas including: Regulatory Compliance, Quality Operations, Validation, Manufacturing, Training and Technical Support. Starting, as individual services provider since 2002, Quality Consulting Group has supported clients implementing the latest standards such as Validation Guidance, ICH Guidelines, and Process Excellence and Risk Management tools. Quality Consulting Group has provided expertise in such areas as: business, operational, quality, regulatory and manufacturing strategies; organizational structures; management controls; manufacturing and quality systems methodologies and practices; compliance programs; and accuracy reviews; FDA, EMEA and other regulatory matter
