JT815 - 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:

• Provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
• Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects.
• Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity
• Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems.
• Initiate and complete routine technical tasks.
• Function as a technical expert to equipment or systems regarding troubleshooting operations.
• Routinely monitor manufacturing processes for performance indicators and operations. Suggest problem resolution and provide troubleshooting guidance.
• 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 chemical engineering, Mechanical Engineering, and Electrical engineering fields are preferable.
• 2 years of Engineering experience
• Preferably, resource should have experience in GMP-related field (manufacturing operations, engineering operations).
• Resource should be capable of resolving equipment related problems by using technical skills to analyze the condition, understand variables that impact the process, and propose and resolve issue.
• Resource should understand control systems (input, output, control).
• Experience in drug substance/API operations.
• Preferred experience in equipment starts up, troubleshooting, PLC.
• Candidate must be able to understand manufacturing equipment, failure modes and troubleshoot equipment (valves, pumps, utilities systems).
• Candidate should be excellent self-learning skills and use technology to his/her advantage.
• Non-Standard Shift 12hrs (5pm to 5am)