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, basic principles and procedures. Assistance given for unusual problems.
• Function as a technical expert to process, equipment and/or systems during troubleshooting operations and multi-functional discussions.
• Frequently become actively involved in daily operations when required to meet schedules or to resolve sophisticated problems.
• Routinely supervise manufacturing processes for performance indicators and operations. Suggest problem resolution and provide troubleshooting mentorship.
• Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process and/or system modifications.

Qualifications:

• Bachelor degree in Chemical, Mechanical or Electrical Engineering (Preferable)
• 2 years of Engineering experience
• 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 start up, troubleshooting, PLC.
• Understand manufacturing equipment, failure modes and troubleshoot equipment (valves, pumps, utilities systems).
• Shift 5:00pm- 5:00am