JT566 - ENGINEER

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:

• Provide solutions to a variety of technical problems of moderate scope and complexity. 
• Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems.
• Perform assignments that have clear and specific objectives and require investigation of limited number of variables.
• Initiate and complete routine technical tasks.
• Function as a technical expert to equipment or systems regarding troubleshooting operations.
• Frequently become actively involved in daily operations when required to meet schedules or to resolve complex problems.
• Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of significant complexity.
• Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications.

Qualifications:

• Bachelor's degree in Engineering & 2 years of Engineering experience
• Previous experiences in any regulated environment (Biotechnology, Pharmaceutical, Medical Devices, etc.).
• Experience in Validation with preference in Process Validation.
• Shift: 8hrs | Due to the nature of the work (support to new product introductions, projects optimization and commercial manufacturing) in some cases, non-standard shift might be required (coverage outside day shift such as second/third shifts, weekends, holidays)