JT878 - 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, basic principles and procedures
• 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
• Support the execution of manufacturing/quality systems such as deviations, equipment qualification and/or process validation, procedures, training, and new product introductions
• Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations
• Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of moderate scope and complexity
• Apply basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects
• Support 7/24 non-standard shift operation including extended hours and weekends as per business needs

Qualifications:
• Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, Industrial, or related field).
• Experience supporting HVAC, utilities, and facility systems within a regulated pharmaceutical or biotechnology environment.
• Knowledge of GMP requirements and applicable regulatory standards.
• Experience in troubleshooting, optimizing, and modifying facility systems.
• Knowledge of preventive maintenance strategies, facility modifications, and capital projects.
• Ability to collaborate with cross-functional teams, including Facilities, Maintenance, Manufacturing, Quality, Validation, and EHS.
• Ability to coordinate with external engineering firms and service providers.
• Strong analytical, problem-solving, and communication skills
• Nonstandar shift 12hr.